Crystallography Open Database

Result: there are 10048 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Searching journal of publication like 'Organic Letters'

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 11 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1555060 CIFC16 H17 N O4P 1 21 16.9082; 11.2913; 19.3834
90; 91.357; 90		1511.53Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555061 CIFC34 H22 Cl2 N4 O4P b c a10.6177; 21.038; 26.249
90; 90; 90		5863.4Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555077 CIFC30 H22 Cl2 N4 O12P 4310.6627; 10.6627; 29.5381
90; 90; 90		3358.3Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555078 CIFC29 H20 I4 O4P -112.1779; 21.8512; 21.9539
60.52; 87.603; 86.921		5077.5Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555080 CIFC38 H26 Cl2 O4P 1 21/c 113.2235; 24.195; 10.2868
90; 110.556; 90		3081.6Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555083 CIFC19 H21 N O4 SP 1 21/n 18.2569; 11.0688; 20.1396
90; 95.9683; 90		1830.66Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555086 CIFC27 H27 N O5 SP 1 21/n 110.98; 21.409; 11.347
90; 104.07; 90		2587.3Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555089 CIFC38 H34 P2P -18.6263; 12.097; 16.023
107.86; 95.73; 104.279		1514.1Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555090 CIFC32 H32 O P2P 1 21/c 114.7596; 10.4392; 17.7877
90; 105.924; 90		2635.5Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555091 CIFC18 H23 N O2P 1 21/c 112.58; 15.83; 8.839
90; 109.551; 90		1658.7Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555095 CIFC19 H16 O2C 1 2 117.095; 5.874; 15.476
90; 106; 90		1493.8Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555096 CIFC21 H13 Cl I3 N O2P -18.885; 11.599; 11.638
87.07; 72.279; 76.183		1109.11Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555100 CIFC21 H15 Cl I N O2P 1 21/n 111.057; 13.631; 13.716
90; 110.38; 90		1937.8Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555102 CIFC22 H22 OP -19.1622; 9.508; 10.568
83; 65.519; 78.417		820Manojveer, Seetharaman; Balamurugan, Rengarajan
In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes.
Organic letters, 2015, 17, 3600-3603
1555105 CIFC8 H10 O4P c a 2110.571; 5.838; 12.338
90; 90; 90		761.4Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555106 CIFC12 H14 O6F d d 237.2102; 18.06; 6.8155
90; 90; 90		4580.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555107 CIFC10 H12 O3P b c a8.8394; 8.5924; 23.437
90; 90; 90		1780.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555108 CIFC9 H12 O4P 21 21 216.345; 8.9881; 15.108
90; 90; 90		861.6Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555109 CIFC8 H10 O4P 1 21 15.3883; 12.812; 6.0438
90; 114.32; 90		380.21Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555112 CIFC19 H22 N2 OP 21 21 217.4987; 12.2482; 16.8063
90; 90; 90		1543.58Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.
Organic letters, 2015, 17, 3628-3631
1555114 CIFC18 H23 N O5 SP 18.6291; 9.4332; 12.4474
82.659; 70.506; 68.236		887.04Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555119 CIFC12 H15 F N2 O4 SP 1 21/n 16.70613; 8.92562; 21.9646
90; 91.7362; 90		1314.12Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555122 CIFC11 H14 N2 O2 SP 1 21/n 115.2033; 5.10542; 15.6074
90; 108.006; 90		1152.1Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555124 CIFC16 H16 N2 O2 SP 1 21/n 18.236; 21.1919; 8.4904
90; 103.856; 90		1438.76Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555126 CIFC13 H19 N O3 SP 21 21 217.789; 11.669; 15.029
90; 90; 90		1366Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555128 CIFC14 H17 Br Cl N O4 SP 1 21 19.24; 6.262; 14.504
90; 91.561; 90		838.9Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555130 CIFC20 H24 Br N O4 SP 1 21 114.656; 10.051; 14.998
90; 104.87; 90		2135.3Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555133 CIFC14 H18 Br N O4 SP 1 21 16.4495; 15.276; 8.0516
90; 96.47; 90		788.2Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555134 CIFC20 H23 Br Cl N O4 SP 21 21 217.6751; 12.59; 22.275
90; 90; 90		2152.4Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555135 CIFC40 H41 N O4 S2P -111.0456; 12.0988; 14.8761
68.867; 70.725; 86.448		1746.7Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555148 CIFC43 H48 N O3 S2P 21 21 2111.13642; 14.74032; 46.2616
90; 90; 90		7594.04Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555149 CIFC8 H8 N2 O4P 21 21 214.888; 9.8; 18.388
90; 90; 90		880.8Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi
Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.
Organic letters, 2015, 17, 4666-4669
1555151 CIFC21 H23 N OP 1 21/c 19.1308; 14.0389; 14.7904
90; 106.943; 90		1813.6Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán
Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives.
Organic letters, 2015, 17, 4136-4139
1555154 CIFC14 H11 Cl N2P 1 21/n 115.4081; 7.7461; 19.9246
90; 98.208; 90		2353.69Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555155 CIFC19 H14 Cl N2 O PP 1 21/c 111.949; 8.5662; 17.479
90; 103.621; 90		1738.8Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555158 CIFC7 H3 Cl2 N2P b c a11.4945; 7.5152; 17.4299
90; 90; 90		1505.66Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555161 CIFC23 H24 O4P 1 21/c 18.759; 21.523; 10.067
90; 104.55; 90		1837Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555162 CIFC18 H20 O6P 1 21/c 17.7505; 21.813; 9.5132
90; 94.65; 90		1603Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555163 CIFC16.5 H16 Cl1.5 N2 O3P 1 21/c 116.298; 11.852; 9.939
90; 90.99; 90		1919.6Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555165 CIFC17 H17 Br O5P b c a11.48; 10.279; 26.181
90; 90; 90		3089.4Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555167 CIFC18 H20 O5P 1 21/c 110.526; 19.394; 7.8119
90; 96.58; 90		1584.2Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555170 CIFC22 H26 O7P 21 21 219.136; 10.6809; 42.2825
90; 90; 90		4126Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555171 CIFC23 H28 O7P 21 21 218.5586; 9.2119; 27.3349
90; 90; 90		2155.11Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555172 CIFC34 H30 N2 O6P 1 21/n 111.4637; 45.4434; 12.0124
90; 116.324; 90		5608.9Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong
Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines.
Organic letters, 2015, 17, 4176-4179
1555175 CIFC26 H18 N4 O5P -19.141; 10.706; 12.0986
73.26; 68.76; 72.31		1030.1Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555177 CIFC21 H15 N3 O3P 1 21/c 116.334; 13.572; 7.87
90; 104.13; 90		1691.9Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555181 CIFC24 H19 N2 O2 S2P 1 21/c 18.3103; 22.0934; 11.8386
90; 104.267; 90		2106.56Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555183 CIFC48 H38 Cl2 N4 O4 S4P 21 21 2112.652; 19.153; 22.403
90; 90; 90		5428.8Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555187 CIFC19 H21 Cl2 N O2 SP 21 21 216.1472; 11.724; 27.834
90; 90; 90		2006Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555188 CIFC19 H20 Cl N O2 SP 1 21 110.133; 9.753; 19.638
90; 100.289; 90		1909.6Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555192 CIFC19 H20 Cl N O2 SP 21 21 218.434; 9.511; 23.843
90; 90; 90		1913Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555194 CIFC25 H19 N3 OP 21 21 217.2944; 14.078; 19.047
90; 90; 90		1955.9Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555196 CIFC21 H19 N3 OP b c a12.7097; 15.6515; 17.3613
90; 90; 90		3453.6Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555197 CIFC22 H34 N4 O9P -19.7492; 10.793; 12.316
106.75; 97.22; 95.45		1219.3Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun
(+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp.
Organic letters, 2015, 17, 4216-4219
1555206 CIFC26 H24 N4 O4C 1 c 19.0718; 20.806; 12.975
90; 107.07; 90		2341.1Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao
Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides.
Organic letters, 2015, 17, 4220-4223
1555207 CIFC42 H22 F6P -19.9256; 11.9918; 12.9082
90.335; 100.557; 103.488		1466.85Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555208 CIFC42 H22 F6P b c a9.5341; 17.1742; 34.8068
90; 90; 90		5699.3Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555211 CIFC65 H65 Cl3 N4 O6 ZnP 4318.5406; 18.5406; 21.1268
90; 90; 90		7262.4Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555213 CIFC70 H77 Cl1.5 N4 O5 ZnC 1 2/c 139.3331; 14.7758; 28.6914
90; 131.696; 90		12450.8Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555214 CIFC67 H71 N4 O5 ZnP -116.9996; 24.3355; 32.7331
89.3681; 83.194; 89.522		13444.9Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555216 CIFC14 H11 N3C 1 2/c 114.857; 12.127; 13.289
90; 106.898; 90		2290.9Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy.
Organic letters, 2015, 17, 4236-4239
1555218 CIFC33 H23 Cl3 N2 O2P 1 21 19.07268; 11.9732; 13.4535
90; 106.945; 90		1397.99Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555219 CIFC32.5 H26 N2 O3.5P 21 21 211.4574; 24.0028; 9.1294
90; 90; 90		2510.67Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555220 CIFC34 H24 O2P 21 21 211.1679; 24.1852; 9.1499
90; 90; 90		2471.37Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555221 CIFC32 H22.67 N2 O2.33P 21 21 2110.41941; 18.297; 36.8632
90; 90; 90		7027.75Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555222 CIFC32 H22 N2 O2P 21 21 217.9491; 16.7592; 18.1848
90; 90; 90		2422.6Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555223 CIFC245 H138 Cl10 F24 N8 O32 S8P -116.057; 18.336; 18.879
79.909; 74.398; 79.264		5214Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T.
Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties.
Organic letters, 2015, 17, 4252-4255
1555224 CIFC41 H36 N2 O9P 1 21/c 119.0503; 11.68507; 14.8134
90; 92.939; 90		3293.19Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555225 CIFC40 H32 N2 O9P b c a13.9815; 16.6793; 26.5582
90; 90; 90		6193.4Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555226 CIFC28 H24 N2 O3 SP 21 21 218.9629; 14.1297; 18.6198
90; 90; 90		2358.1Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui
Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst.
Organic letters, 2015, 17, 4260-4263
1555227 CIFC24 H25 F3 I N O4 SP 1 21/c 113.4658; 20.2837; 19.439
90; 100.921; 90		5213.3Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555229 CIFC24 H26 F2 I N O4 SP 1 21/n 112.121; 15.7186; 25.7853
90; 91.321; 90		4911.4Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555230 CIFC23 H25 F2 I N2 O4 SP n a 2124.1416; 10.1959; 20.5376
90; 90; 90		5055.2Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555231 CIFC16 H26 O6P 1 21 16.5502; 13.639; 9.1291
90; 91.21; 90		815.4Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T.
Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.
Organic letters, 2015, 17, 4284-4287
1555233 CIFC22 H36 O6 SiP 1 21 16.395; 46.881; 8.2621
90; 111.164; 90		2309.9Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H.
Synthesis of the A-D Ring System of the Gambieric Acids.
Organic letters, 2015, 17, 4694-4697
1555236 CIFC14 H17 F O2P 21 21 215.8616; 11.0435; 18.6965
90; 90; 90		1210.27Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555237 CIFC23 H23 F N2 O6P -17.9045; 11.1779; 11.7527
91.21; 92.807; 94		1034.33Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555241 CIFC76 H48 O4C 2 2 219.5716; 40.233; 14.5609
90; 90; 90		5607.3Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555242 CIFC26 H18 O2C 2 2 219.6233; 28.1324; 14.4388
90; 90; 90		3908.97Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555243 CIFC26 H18 Br2 O2C 2 2 219.5385; 16.362; 14.106
90; 90; 90		2201.5Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555244 CIFC76 H78 O16 S4P 43 21 213.3557; 13.3557; 44.138
90; 90; 90		7873.1Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555249 CIFC40 H34 Br N3 O3P 21 21 2112.8306; 13.8096; 19.054
90; 90; 90		3376.1Jing, Changcheng; Xing, Dong; Hu, Wenhao
Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles.
Organic letters, 2015, 17, 4336-4339
1555251 CIFC18 H16 O SP 1 21/n 15.3543; 15.615; 17.226
90; 93.57; 90		1437.4Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555254 CIFC24 H16 O SP 1 21/c 19.1038; 11.532; 16.523
90; 101.54; 90		1699.6Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555256 CIFC21 H30 O4 SiP 1 21/c 115.86; 8.9849; 32.138
90; 117.571; 90		4059.6Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555257 CIFC20 H28 O3 SiC 1 2/c 134.403; 6.7764; 16.1333
90; 92.333; 90		3758Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555258 CIFC9 H5 Cl2 N3 SP b c a6.9189; 13.8264; 21.5767
90; 90; 90		2064.1Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A.
Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine.
Organic letters, 2015, 17, 4118-4121
1555276 CIFC23 H42 N4 O9P 3213.414; 13.414; 13.869
90; 90; 120		2161Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555277 CIFC32.33333 H57.66667 N6 O12.66667P 115.4725; 16.0538; 16.749
107.8; 106.461; 106.157		3482.3Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555278 CIFC39 H70 N8 O15P 1 21 19.319; 23.446; 11.396
90; 108.442; 90		2362.1Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555279 CIFC37 H54 N6 O8P 1 21 111.813; 9.272; 19.747
90; 104.524; 90		2093.8Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555280 CIFC44 H71 N7 O12P 6127.637; 27.637; 11.845
90; 90; 120		7835Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555281 CIFC43 H69 N3 O12P 21 21 2111.226; 12.666; 33.431
90; 90; 90		4753.5Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.
γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.
Organic letters, 2015, 17, 4738-4741
1555283 CIFC18 H28 O7P 1 21 19.874; 10.305; 18.765
90; 99.09; 90		1885.4Chaudhary, Sandeep; Sharma, Vashundhra; Jaiswal, Pradeep K.; Gaikwad, Anil N.; Sinha, Sudhir K.; Puri, Sunil K.; Sharon, Ashoke; Maulik, Prakas R.; Chaturvedi, Vinita
Stable Tricyclic Antitubercular Ozonides Derived from Artemisinin.
Organic letters, 2015, 17, 4948-4951
1555284 CIFC19 H29 N OC 1 2/c 127.579; 8.3362; 17.969
90; 122.94; 90		3467Cheng, Yong-Feng; Rong, Hao-Jie; Yi, Cheng-Bo; Yao, Jun-Jun; Qu, Jin
Redox-Triggered α-C-H Functionalization of Pyrrolidines: Synthesis of Unsymmetrically 2,5-Disubstituted Pyrrolidines.
Organic letters, 2015, 17, 4758-4761
1555291 CIFC28 H22 Cl N2 O2 P SP 1 21/n 19.87691; 17.4624; 14.111
90; 101.632; 90		2383.81Takada, Hisashi; Kumagai, Naoya; Shibasaki, Masakatsu
Stereoselective Total Synthesis of KAE609 via Direct Catalytic Asymmetric Alkynylation to Ketimine.
Organic letters, 2015, 17, 4762-4765
1555293 CIFC9 H7 N O2P 1 21/n 14.4189; 10.48312; 16.03096
90; 95.3299; 90		739.405Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian
Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.
Organic letters, 2015, 17, 5156-5159
1555294 CIFC14 H13 N3 O3 SP n a 218.9685; 11.8374; 12.3725
90; 90; 90		1313.51Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian
Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.
Organic letters, 2015, 17, 5156-5159
1555296 CIFC21 H22 N2 O6 SP -110.449; 10.564; 10.913
65.028; 72.368; 76.052		1031.7Xu, Changming; Zhang, Long; Luo, Sanzhong
Catalytic Asymmetric Oxidative α-C-H N,O-Ketalization of Ketones by Chiral Primary Amine.
Organic letters, 2015, 17, 4392-4395
1555300 CIFC35 H44 N6 O9 SP -18.5759; 13.69; 15.1168
94.615; 91.322; 103.134		1721.18Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz
A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.
Organic letters, 2015, 17, 4774-4777
1555301 CIFC34 H43 N7 O11 SP 1 21/n 113.5559; 16.9708; 16.5586
90; 103.987; 90		3696.43Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz
A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.
Organic letters, 2015, 17, 4774-4777
1555303 CIFC10 H9 N3 OP 1 21/n 117.897; 4.7536; 21.443
90; 105.729; 90		1756Nguyen, Thanh Binh; Corbin, Mathilde; Retailleau, Pascal; Ermolenko, Ludmila; Al-Mourabit, Ali
Elements as Direct Feedstocks for Organic Synthesis: Fe/I2/O2 for Diamination of 2-Cyclohexenones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2015, 17, 4956-4959
1555304 CIFC36 H26 N2 O4 S2P -110.972; 11.356; 12.6933
105.75; 96.509; 100.348		1475.31Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro
Fluorescent Photochromic Diarylethene That Turns on with Visible Light.
Organic letters, 2015, 17, 4802-4805
1555305 CIFC36 H26 N2 O4 S2P -17.8828; 13.6596; 14.9014
112.825; 96.4272; 96.2488		1449.13Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro
Fluorescent Photochromic Diarylethene That Turns on with Visible Light.
Organic letters, 2015, 17, 4802-4805
1555306 CIFC18 H18 N2 O4P 1 21/c 111.3073; 12.3863; 11.762
90; 103.475; 90		1601.99Deng, Guisheng; Wang, Feng; Lu, Shengle; Cheng, Bo
Synthesis of Pyrano[3,2-c]pyrazol-7(1H)-one Derivatives by Tandem Cyclization of 2-Diazo-3,5-dioxo-6-ynoates (Ynones).
Organic letters, 2015, 17, 4651-4653
1555307 CIFC16 H22 O5P 1 21/c 113.19; 10.5762; 12.1985
90; 109.1; 90		1608Gao, Bao; Xie, Yinjun; Shen, Zhiqiang; Yang, Lei; Huang, Hanmin
Decarboxylative Alkylcarboxylation of α,β-Unsaturated Acids Enabled by Copper-Catalyzed Oxidative Coupling.
Organic letters, 2015, 17, 4968-4971
1555308 CIFC17 H13 N O3P 21 21 217.1386; 8.0009; 23.6032
90; 90; 90		1348.1Cheng, Tanyu; Ye, Qunqun; Zhao, Qiankun; Liu, Guohua
Dynamic Kinetic Resolution of Phthalides via Asymmetric Transfer Hydrogenation: A Strategy Constructs 1,3-Distereocentered 3-(2-Hydroxy-2-arylethyl)isobenzofuran-1(3H)-one.
Organic letters, 2015, 17, 4972-4975
1555309 CIFC17 H12 N2 OP -16.9324; 8.0825; 12.0884
92.847; 95.144; 94.822		671.09Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555310 CIFC19 H14 N2 OP b c a14.5086; 13.0756; 15.3147
90; 90; 90		2905.3Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555311 CIFC21 H20 N2 O3P 1 21/c 19.9575; 10.3499; 34.9584
90; 95.625; 90		3585.4Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555312 CIFC23 H22 N2 O3P 1 21/n 112.4989; 10.3089; 15.2366
90; 91.7; 90		1962.37Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark
Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.
Organic letters, 2015, 17, 4838-4841
1555313 CIFC25 H17 ClP 1 21 110.027; 5.4598; 16.953
90; 106.348; 90		890.6Mendis, Shehani N.; Tunge, Jon A.
Palladium-Catalyzed Stereospecific Decarboxylative Benzylation of Alkynes.
Organic letters, 2015, 17, 5164-5167
1555314 CIFC20 H18 F3 N3 O5P 21 21 218.1216; 11.5944; 21.1982
90; 90; 90		1996.1Henderson, Alexander S.; Medina, Sandra; Bower, John F.; Galan, M. Carmen
Nucleophilic Aromatic Substitution (SNAr) as an Approach to Challenging Carbohydrate-Aryl Ethers.
Organic letters, 2015, 17, 4846-4849
1555315 CIFC22 H17 PP 1 21 112.1722; 5.9237; 12.6791
90; 115.892; 90		822.45Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555316 CIFC22 H17 As Au ClP 1 21/c 18.5323; 19.1547; 12.0545
90; 99.9913; 90		1940.23Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555317 CIFC22 H17 Au Cl PP b c a9.915; 17.298; 22.652
90; 90; 90		3885Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555318 CIFC24 H21 As O2P n m a7.88163; 16.2823; 15.3253
90; 90; 90		1966.71Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555319 CIFC22 H17 AsP 1 21 112.2262; 6.03311; 12.5465
90; 115.216; 90		837.26Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke
Practical Synthesis and Properties of 2,5-Diarylarsoles.
Organic letters, 2015, 17, 4854-4857
1555320 CIFC21 H17 NP c a 2120.9818; 8.85852; 8.04013
90; 90; 90		1494.4Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555321 CIFC22 H20 B F4 NP -18.30165; 11.9912; 19.0328
81.1115; 89.9577; 75.0852		1807.32Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555322 CIFC22 H20 I NP 1 21/c 18.35321; 18.1932; 12.3367
90; 109.572; 90		1766.51Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri
A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.
Organic letters, 2015, 17, 4862-4865
1555323 CIFC20 H16 Cl N3 O6P 1 21 16.5669; 20.611; 7.3177
90; 92.8; 90		989.3He, Fu-Sheng; Zhu, Han; Wang, Zheng; Gao, Ming; Yu, Xingxin; Deng, Wei-Ping
Asymmetric Construction of 3,4-Diamino Pyrrolidines via Chiral N,O-Ligand/Cu(I) Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Phthalimidonitroethene.
Organic letters, 2015, 17, 4988-4991
1555324 CIFC51 H53 Cl2 N5 O3P 1 21/c 111.813; 18.382; 21.241
90; 92.944; 90		4606Tian, Yaming; Tian, Lumin; He, Xiang; Li, Chunju; Jia, Xueshun; Li, Jian
Indium(III) Chloride-Catalyzed Isocyanide Insertion Reaction to Construct Complex Spirooxindole.
Organic letters, 2015, 17, 4874-4877
1555325 CIFC17 H31 SiP -16.5951; 11.238; 12.03
105.996; 93.545; 94.888		850.6Sabbasani, Venkata R.; Lee, Daesung
Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.
Organic letters, 2015, 17, 4878-4881
1555326 CIFC13 H23 SiP -16.2702; 10.955; 11.088
75.965; 74.11; 74.699		694.6Sabbasani, Venkata R.; Lee, Daesung
Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.
Organic letters, 2015, 17, 4878-4881
1555327 CIFC15 H10 Cl F2 NP 1 21/n 16.5538; 13.9376; 13.754
90; 92.544; 90		1255.11Aikawa, Kohsuke; Maruyama, Kenichi; Honda, Kazuya; Mikami, Koichi
α-Difluoromethylation on sp(3) Carbon of Nitriles Using Fluoroform and Ruppert-Prakash Reagent.
Organic letters, 2015, 17, 4882-4885
1555328 CIFC35 H30 Br F N4 O4P 18.4125; 9.7659; 11.5692
108.577; 95.876; 110.228		820.9Bao, Xiaoze; Wang, Baomin; Cui, Longchen; Zhu, Guodong; He, Yuli; Qu, Jingping; Song, Yuming
An Organocatalytic Asymmetric Friedel-Crafts Addition/Fluorination Sequence: Construction of Oxindole-Pyrazolone Conjugates Bearing Vicinal Tetrasubstituted Stereocenters.
Organic letters, 2015, 17, 5168-5171
1555329 CIFC17 H13 Cl O2F d d 224.4402; 52.631; 4.31801
90; 90; 90		5554.3Suzuki, Takeyuki; Ismiyarto, ?; Ishizaka, Yuka; Zhou, Da-Yang; Asano, Kaori; Sasai, Hiroaki
One-Pot Catalysis Using a Chiral Iridium Complex/Brønsted Base: Catalytic Asymmetric Synthesis of Catalponol.
Organic letters, 2015, 17, 5176-5179
1555330 CIFC21 H15 F3 N2P 1 21/c 119.794; 11.828; 7.3236
90; 91.476; 90		1714.1Tang, Mi; Tong, Lingfeng; Ju, Lei; Zhai, Wanwan; Hu, Yang; Yu, Xinhong
Benzoic Acid Catalyzed Annulations of α-Amino Acids and Aromatic Aldehydes Containing an ortho-Michael Acceptor: Access to 2,5-Dihydro-1H-benzo[c]azepines and 10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a]azepines.
Organic letters, 2015, 17, 5180-5183
1555331 CIFC18 H22 N2 O2P 1 21/c 18.34; 25.16; 8.134
90; 109.63; 90		1608Yuan, Jingwen; Zhang, Qian; Yu, Mangfei; Huang, Peng; Zhang, Rui; Dong, Dewen
Phenyliodine(III) Diacetate Mediated Oxidative Cyclization of 1-Alkenoyl-1-carbamoyl Cycloalkanes: Access to Spiro-Fused Dihydrofuran-3(2H)-ones.
Organic letters, 2015, 17, 5012-5015
1555332 CIFC24 H15 F2 N O2P -18.126; 9.511; 12.21
84.646; 78.696; 74.768		892Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555333 CIFC44 H36 F4 N2 O4 Si2P 1 21/c 16.2172; 11.8634; 29.226
90; 94.257; 90		2149.7Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555334 CIFC34 H20 F4 N2 O4P 1 21/c 117.755; 9.629; 15.724
90; 99.347; 90		2652.5Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo
Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.
Organic letters, 2015, 17, 5016-5019
1555335 CIFC51 H46 F12 N6 Ni O16 S4P 1 21 113.6455; 18.1359; 24.9551
90; 104.465; 90		5979.9Takeda, Takuya; Harada, Shinji; Nishida, Atsushi
Catalytic Asymmetric Nazarov Cyclization of Heteroaryl Vinyl Ketones through a Crystallographically Defined Chiral Dinuclear Nickel Complex.
Organic letters, 2015, 17, 5184-5187
1555336 CIFC26 H18 Br N O2P 1 21/n 110.612; 16.848; 23.394
90; 96.68; 90		4154.2Liang, Ling; Li, Erqing; Dong, Xuelin; Huang, You
DABCO-Mediated [4 + 4]-Domino Annulation: Access to Functionalized Eight-Membered Cyclic Ethers.
Organic letters, 2015, 17, 4914-4917
1555337 CIFC17 H20 O3P 1 21 18.3018; 14.7835; 12.3636
90; 101.126; 90		1488.86Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.
Organic letters, 2015, 17, 5040-5043
1555338 CIFC17 H20 O3P -18.0539; 9.0826; 9.9175
102.862; 97.071; 96.384		694.648Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.
Organic letters, 2015, 17, 5040-5043
1555339 CIFC22 H28 O3P 21 21 2111.3754; 11.9359; 14.185
90; 90; 90		1925.98Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun
Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.
Organic letters, 2015, 17, 5040-5043
1555340 CIFC81 H22 O S2C 1 2/c 145.917; 10.214; 19.5587
90; 104.361; 90		8886.3Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
1555341 CIFC79 H22 OP -19.9134; 14.8425; 17.0648
67.983; 89.643; 77.467		2264.5Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
1555342 CIFC80 H24 OP 1 21/c 114.971; 17.4948; 16.7353
90; 107.46; 90		4181.3Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang
Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.
Organic letters, 2015, 17, 5192-5195
1555343 CIFC13 H21 N O2P 21 21 216.0749; 8.2818; 25.017
90; 90; 90		1258.6Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555344 CIFC11 H19 N O2P 21 21 2110.7069; 10.8672; 19.656
90; 90; 90		2287.1Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555345 CIFC15 H19 N O3P 1 21 15.8171; 7.1215; 16.2736
90; 94.53; 90		672.05Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555346 CIFC9 H15 N O2P 1 21 16.1254; 6.9441; 10.8047
90; 102.426; 90		448.82Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555347 CIFC8 H11 N O2P 21 21 216.742; 7.2944; 15.8577
90; 90; 90		779.86Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555348 CIFC13 H13 N O3P 1 21 18.236; 6.3687; 10.9331
90; 92.94; 90		572.71Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.
Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.
Organic letters, 2015, 17, 5204-5207
1555349 CIFC24 H40 O8P 1 21 17.32024; 8.9338; 17.2413
90; 91.3123; 90		1127.24Wu, Ping; Xue, Jinghua; Yao, Lei; Xu, Liangxiong; Li, Hanxiang; Wei, Xiaoyi
Bisacremines E-G, Three Polycyclic Dimeric Acremines Produced by Acremonium persicinum SC0105.
Organic letters, 2015, 17, 4922-4925
1555350 CIFC25 H25 N O9P -110.925; 10.939; 11.295
113.793; 97.632; 99.629		1187.3Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin
Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.
Organic letters, 2015, 17, 5216-5219
1555351 CIFC25 H22 O6P -110.167; 11.5366; 11.951
68.165; 67.543; 79.903		1201.6Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin
Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.
Organic letters, 2015, 17, 5216-5219
1555352 CIFC24 H20 O2P 1 21/c 110.2764; 23.0983; 7.47
90; 101.197; 90		1739.4Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides.
Organic letters, 2015, 17, 5220-5223
1555353 CIFC21 H24 Br N OP -18.3568; 9.126; 13.2967
72.212; 72.822; 85.148		922.49Wong, Ying-Chieh; Ke, Zhihai; Yeung, Ying-Yeung
Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide.
Organic letters, 2015, 17, 4944-4947
1555354 CIFC18 H32 N2 OP 21 21 215.287; 9.4826; 34.033
90; 90; 90		1706.23Bosch, Caroline; Fiser, Béla; Gómez-Bengoa, Enrique; Bradshaw, Ben; Bonjoch, Josep
Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine E and Putative Structure of (-)-Huperzine N.
Organic letters, 2015, 17, 5084-5087
1555355 CIFC24 H24 Br N O4P 21 21 216.6742; 12.874; 25.688
90; 90; 90		2207.2Das, Tapas; Saha, Prasenjit; Singh, Vinod K.
Silver(I)-Ferrophox Catalyzed Enantioselective Desymmetrization of Cyclopentenedione: Synthesis of Highly Substituted Bicyclic Pyrrolidines.
Organic letters, 2015, 17, 5088-5091
1555356 CIFC98 H156 Cd4 Cl14 Lu2 N56 O62P n m a35.112; 12.3662; 19.6459
90; 90; 90		8530.3Zhao, Wen-Xuan; Wang, Chuan-Zeng; Chen, Li-Xia; Cong, Hang; Xiao, Xin; Zhang, Yun-Qian; Xue, Sai-Feng; Huang, Ying; Tao, Zhu; Zhu, Qian-Jiang
A Hemimethyl-Substituted Cucurbit[7]uril Derived from 3α-Methyl-glycoluril.
Organic letters, 2015, 17, 5072-5075
1555357 CIFC21 H16 F2 OP -18.2834; 10.8217; 18.382
78.708; 82.706; 89.789		1602.4Yang, Chao; Xu, Zheng-Liang; Shao, Hui; Mou, Xue-Qing; Wang, Jie; Wang, Shao-Hua
A Tin(IV) Chloride Promoted Tandem C-O Bond Cleavage/Nazarov Cyclization/Nucleophilic Addition Reaction of 1,1-Disubstituted Allylic Ethers toward the Synthesis of Multisubstituted Indenes.
Organic letters, 2015, 17, 5288-5291
1555358 CIFC25 H26 F6 N3 P PdP 21 21 219.6947; 12.5617; 21.062
90; 90; 90		2565Álvarez-Casao, Yolanda; Monge, David; Álvarez, Eleuterio; Fernández, Rosario; Lassaletta, José M
Pyridine-Hydrazones as N,N'-Ligands in Asymmetric Catalysis: Pd(II)-Catalyzed Addition of Boronic Acids to Cyclic Sulfonylketimines.
Organic letters, 2015, 17, 5104-5107
1555359 CIFC19 H23 F2 N O3P 1 21 112.3361; 6.0532; 13.2095
90; 115.922; 90		887.15Aikawa, Kohsuke; Yoshida, Seiya; Kondo, Daisuke; Asai, Yuya; Mikami, Koichi
Catalytic Asymmetric Synthesis of Tertiary Alcohols and Oxetenes Bearing a Difluoromethyl Group.
Organic letters, 2015, 17, 5108-5111
1555360 CIFC38 H30 N2 O4 S2P -19.37; 12.582; 14.702
90.83; 105.888; 110.831		1546Dhiman, Seema; Ramasastry, S. S. V.
One-Pot Relay Gold(I) and Brønsted Acid Catalysis: Cyclopenta[b]annulation of Indoles via Hydroamination/Nazarov-Type Cyclization Cascade of Enynols.
Organic letters, 2015, 17, 5116-5119
1555361 CIFC60 H60 Cl2 N4 O4 RuP -112.0889; 12.4331; 18.0531
75.323; 86.447; 89.594		2619.7Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555362 CIFC22 H24 N2 O4 SP 1 21/c 115.928; 11.573; 11.95
90; 107.075; 90		2105.7Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555363 CIFC24 H23 N O2 SP 1 21/c 116.4534; 8.1341; 16.6107
90; 116.278; 90		1993.3Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555364 CIFC22 H25 N O2 SP -18.1967; 9.0717; 15.216
87.208; 82.37; 65.005		1016.4Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro
Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.
Organic letters, 2015, 17, 5284-5287
1555365 CIFC24 H25 Br N2 O4 SC 1 2 19.512; 19.054; 30.838
90; 93.81; 90		5577Shu, Xing-zhong; Schienebeck, Casi M.; Li, Xiaoxun; Zhou, Xin; Song, Wangze; Chen, Lianqing; Guzei, Ilia A.; Tang, Weiping
Rhodium-Catalyzed Stereoselective Intramolecular [5 + 2] Cycloaddition of 3-Acyloxy 1,4-Enyne and Alkene.
Organic letters, 2015, 17, 5128-5131
1555366 CIFC19 H20 N2 O3P 1 21/c 112.4342; 16.375; 8.6369
90; 106.914; 90		1682.49Sar, Dinabandhu; Bag, Raghunath; Yashmeen, Afsana; Bag, Subhendu Sekhar; Punniyamurthy, Tharmalingam
Synthesis of Functionalized Pyrazoles via Vanadium-Catalyzed C-N Dehydrogenative Cross-Coupling and Fluorescence Switch-On Sensing of BSA Protein.
Organic letters, 2015, 17, 5308-5311
1555367 CIFC18 H23 N O7P 6510.2093; 10.2093; 30.4222
90; 90; 120		2746.08N V G, Moorthy; Dyapa, Rajendar; Pansare, Sunil V.
Formal Synthesis of (+)-Lasubine II and (-)-Subcosine II via Organocatalytic Michael Addition of a Ketone to an α-Nitrostyrene.
Organic letters, 2015, 17, 5312-5315
1555368 CIFC19 H21 N2 O2.5P 1 21 19.5014; 17.2076; 9.9401
90; 90.682; 90		1625.1Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.
Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.
Organic letters, 2015, 17, 5732-5735
1555369 CIFC42 H46 N4 O5P 1 21/c 121.8506; 6.802; 25.1773
90; 113.248; 90		3438.21Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.
Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.
Organic letters, 2015, 17, 5732-5735
1555370 CIFC19 H16 O5P 1 21 17.0727; 8.9761; 11.4306
90; 96.806; 90		720.56Yang, Chunfang; Huang, Chunshuai; Zhang, Wenjun; Zhu, Yiguang; Zhang, Changsheng
Heterologous Expression of Fluostatin Gene Cluster Leads to a Bioactive Heterodimer.
Organic letters, 2015, 17, 5324-5327
1555371 CIFC14 H11 N O2 S2P 21 21 217.5169; 10.5263; 16.5993
90; 90; 90		1313.42Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555372 CIFC15 H17 N O4 SP 21 21 217.7171; 7.9486; 23.816
90; 90; 90		1460.88Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555373 CIFC16 H13 N O2 SP 4310.7582; 10.7582; 11.4283
90; 90; 90		1322.7Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555374 CIFC14 H11 N O3 SP 21 21 217.5472; 10.3052; 16.2327
90; 90; 90		1262.5Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555375 CIFC11 H11 N O2 SP 21 21 218.0916; 9.4218; 13.8016
90; 90; 90		1052.2Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.
Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.
Organic letters, 2015, 17, 5340-5343
1555376 CIFC24 H21 Br O6P 21 21 216.625; 10.223; 31.029
90; 90; 90		2101.5Liang, Zhi-Qin; Wang, Dong-Ling; Zhang, Han-Ming; Ye, Song
Enantioselective Synthesis of Bicyclic δ-Lactones via N-Heterocyclic Carbene-Catalyzed Cascade Reaction.
Organic letters, 2015, 17, 5140-5143
1555377 CIFC24 H24 F3 N O4C 1 2/c 128.0198; 9.2681; 17.0333
90; 104.376; 90		4284.9Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555378 CIFC21 H21 N2 O4P -19.5002; 9.6957; 10.3129
96.467; 104.739; 98.162		898.32Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555379 CIFC23 H20 F3 N3 OP 1 21/c 113.6453; 9.9432; 14.4487
90; 91.039; 90		1960Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555380 CIFC22 H27 N3 OC 1 2/c 132.003; 7.0392; 19.0154
90; 120.399; 90		3694.8Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555381 CIFC22 H20 N2 O5P c c n22.182; 22.337; 14.877
90; 90; 90		7371Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555382 CIFC24 H22 N2 OP 1 21/c 117.6141; 8.5636; 12.8104
90; 107.202; 90		1845.89Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555383 CIFC25 H24 N2 O2P 1 21/c 117.188; 9.172; 13.025
90; 108.831; 90		1943.5Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming
Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.
Organic letters, 2015, 17, 5368-5371
1555384 CIFC30 H32 B2 F4 N4P 1 2/c 112.718; 8.6639; 12.342
90; 101.101; 90		1334.5Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.
Organic letters, 2015, 17, 5360-5363
1555385 CIFC30 H34 B2 F4 N4P 1 21/n 117.6404; 8.5702; 20.1377
90; 114.568; 90		2768.8Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.
Organic letters, 2015, 17, 5360-5363
1555386 CIFC25 H24 N4 O4P n a 218.7914; 22.2498; 11.9566
90; 90; 90		2338.79Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
1555387 CIFC37 H42 N4 O6P 21 21 217.8202; 15.433; 28.4386
90; 90; 90		3432.2Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
1555388 CIFC34 H34 N4 O4P 1 21 110.2983; 10.6899; 13.1072
90; 94.794; 90		1437.89Chingle, Ramesh; Lubell, William D.
Azopeptides: Synthesis and Pericyclic Chemistry.
Organic letters, 2015, 17, 5400-5403
1555389 CIFC29 H25 Br N2 O3P b c a12.7295; 15.5318; 24.571
90; 90; 90		4858Li, Falin; Chen, Jiangfei; Hou, Yading; Li, Yujie; Wu, Xin-Yan; Tong, Xiaofeng
1,3-Dipolar Cycloadditions of 4-Acetoxy Allenoates: Access to 2,3-Dihydropyrazoles, 2,3-Dihydroisoxazoles, and Indolizines.
Organic letters, 2015, 17, 5376-5379
1555390 CIFC23 H25 N S2P 1 21/c 17.4977; 11.606; 23.037
90; 91.639; 90		2003.8Yamauchi, Takayuki; Shibahara, Fumitoshi; Murai, Toshiaki
Direct C-H Bond Arylation of Thienyl Thioamides Catalyzed by Pd-Phenanthroline Complexes.
Organic letters, 2015, 17, 5392-5395
1555391 CIFC48 H70 Cl I2 N7 OP 21 21 2111.7863; 15.6266; 27.3025
90; 90; 90		5028.57Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555392 CIFC54.5 H73 Cl5 I2 N8P n m a16.4441; 19.3772; 19.7044
90; 90; 90		6278.62Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555393 CIFC37 H35 I2 N7C 1 2/c 150.2116; 8.9517; 25.5239
90; 111.754; 90		10655.4Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555394 CIFC91 H108 Cl3 I4 N15 O4P 1 21/c 120.9995; 15.2694; 28.6315
90; 90.725; 90		9179.9Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555395 CIFC37 H35 I2 N7 O2P 1 21/c 117.3106; 15.673; 15.0038
90; 109.469; 90		3837.91Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.
Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.
Organic letters, 2015, 17, 5740-5743
1555396 CIFC13 H20 N2 O7P 21 21 217.5247; 13.1309; 15.066
90; 90; 90		1488.61Habibian, Maryam; Martínez-Montero, Saúl; Portella, Guillem; Chua, Zhijie; Bohle, D. Scott; Orozco, Modesto; Damha, Masad J.
Seven-Membered Ring Nucleoside Analogues: Stereoselective Synthesis and Studies on Their Conformational Properties.
Organic letters, 2015, 17, 5416-5419
1555397 CIFC62 H73.33 N13 O12R -3 :H20.9278; 20.9278; 11.7428
90; 90; 120		4454Ren, Changliang; Shen, Jie; Zeng, Huaqiang
One-Pot Synthesis of Strained Macrocyclic Pyridone Hexamers and Their High Selectivity toward Cu(2+) Recognition.
Organic letters, 2015, 17, 5946-5949
1555398 CIFC19 H26 O2P 1 21 17.2207; 10.6225; 10.6751
90; 101.193; 90		803.23Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555399 CIFC18 H22 O3P 21 21 217.5988; 8.4424; 21.953
90; 90; 90		1408.33Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555400 CIFC20 H23 N O3P 21 21 217.2672; 12.3762; 18.5597
90; 90; 90		1669.27Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555401 CIFC19 H23 N O2P 1 21 17.5354; 8.5029; 11.9989
90; 90.259; 90		768.79Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.
Organic letters, 2015, 17, 5432-5435
1555402 CIFC22 H15 Cl OP -16.5461; 8.998; 14.2101
92.224; 101.253; 92.809		818.92Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555403 CIFC22 H15 Br OP 1 21/c 16.253; 15.418; 17.593
90; 92.18; 90		1694.9Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555404 CIFC22 H16 OP 1 21/c 116.0902; 5.6098; 17.2424
90; 94.43; 90		1551.7Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555405 CIFC23 H22 Cl N O4P 21 21 225.273; 6.4369; 12.9596
90; 90; 90		2108.3Liu, Hua-Chao; Liu, Kang; Xue, Zhi-Yong; He, Zhao-Lin; Wang, Chun-Jiang
Silver(I)-Catalyzed Enantioselective Desymmetrization of Cyclopentenediones: Access to Highly Functionalized Bicyclic Pyrrolidines.
Organic letters, 2015, 17, 5440-5443
1555406 CIFC17 H15 N O6 SP 1 21 17.5529; 11.091; 10.123
90; 104.11; 90		822.4Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555407 CIFC24 H21 N O6 SP 21 21 217.7963; 11.5859; 23.086
90; 90; 90		2085.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555408 CIFC18 H15 Br2 Cl2 N O5 SP 1 21 111.974; 5.7044; 15.451
90; 95.49; 90		1050.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555409 CIFC20 H19 N O5 SP 21 21 217.7017; 8.4118; 27.288
90; 90; 90		1767.9Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555410 CIFC17 H14 N4 O5 SP 1 21 18.3457; 10.924; 9.879
90; 109.46; 90		849.2Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555411 CIFC17 H14 Br N O5 SP 1 21 18.091; 6.973; 15.224
90; 101.811; 90		840.7Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555412 CIFC17 H12 Br F2 N O5 SP 21 21 216.8957; 12.551; 22.629
90; 90; 90		1958.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555413 CIFC21 H17 N O5 S2C 2 2 2111.289; 10.612; 32.425
90; 90; 90		3884.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555414 CIFC19 H17 Br Cl N O5 SP 21 21 219.155; 9.47; 23.095
90; 90; 90		2002.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555415 CIFC14 H22 O4P 21 21 216.5953; 9.079; 21.403
90; 90; 90		1281.6Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555416 CIFC18 H28 O4 SiP 21 21 217.2691; 11.4811; 21.668
90; 90; 90		1808.4Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555417 CIFC15 H18 O7P 1 21 17.187; 8.7702; 11.015
90; 98.176; 90		687.23Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555418 CIFC17 H16 F6 O9P 1 21/c 113.5602; 8.6298; 17.3709
90; 92.1; 90		2031.4Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555419 CIFC11 H17 O5P 1 21/n 16.4697; 11.6627; 16.0124
90; 93.278; 90		1206.23Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555420 CIFC17 H19 F3 O9P 1 21/c 113.9325; 8.4366; 16.9502
90; 92.536; 90		1990.4Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555421 CIFC24 H31 N O5 SP 21 21 215.8376; 10.6992; 37.5454
90; 90; 90		2345Serpier, Fabien; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Access to Polyfunctionalized Chiral Piperidines through Enantioselective Addition-Carbocyclization Cascade Reaction Catalyzed by a Rhodium(I)-Diene Complex.
Organic letters, 2015, 17, 5496-5499
1555422 CIFC16 H18 Li N2 OP b c n15.9311; 9.7436; 9.2498
90; 90; 90		1435.81Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555423 CIFC28 H32 N2 Si2P 1 21/c 18.4866; 18.1483; 16.7017
90; 97.928; 90		2547.8Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555424 CIFC44 H62 Li2 N4 O2C 1 2/c 126.34; 11.0689; 18.748
90; 134.32; 90		3910.7Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555425 CIFC39 H46 N2 Si2P c a 2113.9869; 12.5966; 19.4789
90; 90; 90		3431.9Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555426 CIFC13 H15 B F N O5P 1 21/c 113.4038; 9.8242; 11.011
90; 110.376; 90		1359.2St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.
Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.
Organic letters, 2015, 17, 5764-5767
1555427 CIFC15.5 H20 B N2 O7.5 SP 1 21/c 110.3226; 15.7804; 11.1047
90; 107.792; 90		1722.38St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.
Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.
Organic letters, 2015, 17, 5764-5767
1555428 CIFC15 H12 Cl2 O S2P n m a6.9371; 9.8082; 22.3442
90; 90; 90		1520.31Huang, Xin; Wang, Jichao; Ni, Zhangqin; Wang, Sichang; Pan, Yuanjiang
Synthesis of α,α-Disulfenylated Aldehydes via Oxidative Transformation of Tertiary Amines.
Organic letters, 2015, 17, 5488-5491
1555429 CIFC82 H54 N4P -110.1789; 11.9937; 13.2135
108.6; 95.189; 102.354		1471.38Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang
Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.
Organic letters, 2015, 17, 6138-6141
1555430 CIFC82 H54 N4P -110.0347; 11.9855; 25.329
77.339; 87.855; 87.767		2968.7Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang
Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.
Organic letters, 2015, 17, 6138-6141
1555431 CIFC20 H15 Cl N2 O5P 1 21 112.275; 11.187; 13.371
90; 104.835; 90		1774.9Gao, Hang; Luo, Zhenli; Ge, Pingjin; He, Junqian; Zhou, Feng; Zheng, Peipei; Jiang, Jun
Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid.
Organic letters, 2015, 17, 5962-5965
1555432 CIFC25.5 H31 Cl1.5 N2 O5 P SP 1 21 113.5437; 13.0346; 16.0277
90; 102.411; 90		2763.4Kayal, Satavisha; Mukherjee, Santanu
Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates.
Organic letters, 2015, 17, 5508-5511
1555433 CIFC19 H18 F3 N O2 SP 1 c 18.9711; 9.9056; 10.1296
90; 94.135; 90		897.8Zhu, Zi-Zhong; Chen, Kai; Yu, Liu-Zhu; Tang, Xiang-Ying; Shi, Min
Copper(I)-Catalyzed Intramolecular Trifluoromethylation of Methylenecyclopropanes.
Organic letters, 2015, 17, 5994-5997
1555434 CIFC40 H20 O3P 1 21/c 17.63737; 22.5914; 15.1095
90; 99.906; 90		2568.11Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555435 CIFC22 H16 O4P n a 2123.0883; 8.2485; 17.6035
90; 90; 90		3352.5Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555436 CIFC24 H24 N4 O3C 1 2 137.9789; 14.5891; 21.4715
90; 119.848; 90		10318.8Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai
One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.
Organic letters, 2015, 17, 5816-5819
1555437 CIFC25 H28 N4 O5P 21 21 218.2785; 9.2956; 29.7576
90; 90; 90		2289.96Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai
One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.
Organic letters, 2015, 17, 5816-5819
1555438 CIFC44 H63 N5 O11P 1 21/c 119.5349; 6.5541; 34.67
90; 95.943; 90		4415.1Tabor, M. Greg; Shenvi, Ryan A.
Synthesis of Lepadiformine Using a Hydroamination Transform.
Organic letters, 2015, 17, 5776-5779
1555439 CIFC15 H15 N OP 1 21 17.0716; 6.6011; 13.3983
90; 92.659; 90		624.76Vita, Maria Victoria; Caramenti, Paola; Waser, Jerome
Enantioselective Synthesis of Homoallylic Azides and Nitriles via Palladium-Catalyzed Decarboxylative Allylation.
Organic letters, 2015, 17, 5832-5835
1555440 CIFC29 H30 Br N3 OP -18.9762; 9.2143; 15.8055
91.311; 97.75; 93.388		1292.4Duan, Xiao-Yong; Yang, Xiu-Long; Jia, Pan-Pan; Zhang, Man; Han, Bing
Hydrazonyl Radical-Participated Tandem Reaction: A Strategy for the Synthesis of Pyrazoline-Functionalized Oxindoles.
Organic letters, 2015, 17, 6022-6025
1555441 CIFC18 H13 N O3P 1 21/n 19.2686; 16.156; 9.4109
90; 95.246; 90		1403.3Sengoku, Tetsuya; Murata, Yusuke; Aso, Yuwa; Kawakami, Ai; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure.
Organic letters, 2015, 17, 5846-5849
1555442 CIFC104 H170 Cl8 Cu2 N16 O17C 1 2/c 125.299; 19.2324; 28.254
90; 91.806; 90		13740Ganss, Alexander; Belda, Raquel; Pitarch, Javier; Goddard, Richard; García-España, Enrique; Kubik, Stefan
Synthesis and Structural Characterization of a Cyclen-Derived Molecular Cage.
Organic letters, 2015, 17, 5850-5853
1555443 CIFC28 H32 Br N3 O3P 1 21/c 116.0245; 8.5681; 19.233
90; 95.076; 90		2630.3Douchez, Antoine; Lubell, William D.
Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.
Organic letters, 2015, 17, 6046-6049
1555444 CIFC20 H15 Br Cl N3 O3P 1 21/n 18.8959; 13.3302; 15.9639
90; 91.132; 90		1892.7Douchez, Antoine; Lubell, William D.
Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.
Organic letters, 2015, 17, 6046-6049
1555445 CIFC24 H21 N5 O2P -18.7322; 9.9954; 12.0561
78.166; 89.574; 82.698		1021.37Ramanathan, Mani; Wang, Yu-Hao; Liu, Shiuh-Tzung
One-Pot Reactions for Synthesis of 2,5-Substituted Tetrazoles from Aryldiazonium Salts and Amidines.
Organic letters, 2015, 17, 5886-5889
1555446 CIFC18 H22 O2P 21 21 219.0068; 10.478; 16.4734
90; 90; 90		1554.65Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei
Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols.
Organic letters, 2015, 17, 6058-6061
1555447 CIFC21 H16 O3P b c a15.108; 7.54; 27.9119
90; 90; 90		3179.6Ravi Kumar, Devarapalli; Satyanarayana, Gedu
Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.
Organic letters, 2015, 17, 5894-5897
1555448 CIFC15 H12 O3P 1 21/n 17.8593; 4.0079; 36.679
90; 93.567; 90		1153.1Ravi Kumar, Devarapalli; Satyanarayana, Gedu
Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.
Organic letters, 2015, 17, 5894-5897
1555449 CIFC20 H30 O2C 1 2 120.0748; 6.8584; 25.9078
90; 106.399; 90		3421.9Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555450 CIFC24 H36 O4P 1 21 111.623; 7.3026; 12.673
90; 95.271; 90		1071.1Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555451 CIFC24 H36 O4C 1 2 131.775; 7.261; 19.184
90; 104.026; 90		4294.1Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555452 CIFC24 H36 O4P 1 21 110.27; 7.257; 14.424
90; 92.479; 90		1074Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555453 CIFC38 H54 O5P 21 21 2110.0955; 13.4185; 24.927
90; 90; 90		3376.8Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555454 CIFC62 H84 N8 O2 S2 Si4P -18.2413; 12.7682; 15.6926
80.64; 82.824; 75.922		1574.06Cortizo-Lacalle, Diego; Gozalvez, Cristian; Olano, Mikel; Sun, Xiangnan; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio
Bisthiadiazole-Fused Tetraazapentacenequinone: An Air-Stable Solution-Processable n-Type Organic Semiconductor.
Organic letters, 2015, 17, 5902-5905
1555455 CIFC31 H23 Cl2 N O4 SP -19.8014; 12.1207; 13.323
99.552; 106.402; 111.742		1343.8Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang
Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.
Organic letters, 2015, 17, 6078-6081
1555456 CIFC30 H21 Cl2 N O3 SP -17.3264; 7.7051; 23.332
84.594; 88.837; 82.404		1299.7Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang
Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.
Organic letters, 2015, 17, 6078-6081
1555457 CIFC23 H18 N2 O3 SP -19.5468; 10.4076; 11.3179
103.653; 93.612; 114.414		978.53Qiao, Huijie; Sun, Suyan; Yang, Fan; Zhu, Yu; Zhu, Weiguo; Dong, Yaxi; Wu, Yusheng; Kong, Xiangtao; Jiang, Ling; Wu, Yangjie
Copper(I)-Catalyzed Sulfonylation of 8-Aminoquinoline Amides with Sulfonyl Chlorides in Air.
Organic letters, 2015, 17, 6086-6089
1555458 CIFC56 H40 F6 N6P 1 21/c 17.398; 11.831; 25.874
90; 94.823; 90		2256.6Tasior, Mariusz; Chotkowski, Maciej; Gryko, Daniel T.
Extension of Pyrrolopyrrole π-System: Approach to Constructing Hexacyclic Nitrogen-Containing Aromatic Systems.
Organic letters, 2015, 17, 6106-6109
1555459 CIFC136 H112 OP -110.6194; 15.7603; 16.3359
73.944; 87.761; 73.938		2522.8He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555460 CIFC62.74 H45.48 Cl1.48P -19.9913; 15.4197; 15.7043
102.428; 92.308; 99.776		2321He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555461 CIFC104 H80 OP -110.2023; 12.2529; 16.1191
98.99; 102.37; 105.55		1846.7He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555462 CIFC52 H40 O0.5P -110.11; 10.19; 36.97
91.2; 94.1; 95.6		3779.3He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555463 CIFC58 H52 OC 1 2/c 130.72; 17.174; 16.373
90; 97.824; 90		8557.7He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555464 CIFC19 H17 Cl N2 O1.425P 1 21/c 113.0804; 18.104; 15.8995
90; 102.512; 90		3675.7Jiang, Pingping; Li, Feng; Xu, Yongbao; Liu, Qingwen; Wang, Jing; Ding, Hong; Yu, Renfu; Wang, Qifeng
Aromaticity-Dependent Regioselectivity in Pd(II)-Catalyzed C-H Direct Arylation of Aryl Ureas.
Organic letters, 2015, 17, 5918-5921
1555465 CIFC21 H14 O4P n a 219.2786; 23.641; 7.5289
90; 90; 90		1651.5Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555466 CIFC15 H12 O3P 1 21/n 113.899; 6.5834; 14.579
90; 117.751; 90		1180.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555467 CIFC20 H14 O2P 21 21 217.3238; 9.814; 19.747
90; 90; 90		1419.3Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555468 CIFC14 H10 O3P 1 21/n 110.271; 9.1771; 11.2051
90; 97.686; 90		1046.7Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555469 CIFC22 H14 O3P b c a12.5409; 7.8473; 31.588
90; 90; 90		3108.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555470 CIFC19 H14 O3P -16.866; 10.24; 11.188
69.311; 72.734; 83.093		702.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555471 CIFC17 H13 N O3P 1 21/c 14.629; 16.421; 17.474
90; 91.158; 90		1328Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555472 CIFC18 H12 O3P -17.4224; 7.787; 12.133
99.775; 91.453; 97.925		683.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555473 CIFC21 H19 N O5P 1 21/c 19.3725; 21.712; 9.3146
90; 106.094; 90		1821.2Hong, Jung-Ho; Atta, Ananta Kumar; Jung, Kwang-Bok; Kim, Seul-Bi; Heo, Jungseok; Cho, Dong-Gyu
Conformationally Locked Tolans, β-Sheet Structures, and Photophysical Properties.
Organic letters, 2015, 17, 6222-6225
1555474 CIFC17 H22 N O3 SP 1 21 18.5345; 8.8037; 11.0062
90; 90.369; 90		826.94Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.
Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.
Organic letters, 2015, 17, 6226-6229
1555475 CIFC13 H18 N3 O4P 1 21 16.1187; 15.5628; 7.4298
90; 90.617; 90		707.46Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.
Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.
Organic letters, 2015, 17, 6226-6229
1555476 CIFC10 H20 O S2 SiP 1 21 16.642; 14.2879; 13.6807
90; 91.605; 90		1297.79Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B
An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.
Organic letters, 2015, 17, 6242-6245
1555477 CIFC18 H34 O S4 SiP -19.7683; 10.4783; 12.5293
102.548; 99.034; 115.038		1088.3Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B
An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.
Organic letters, 2015, 17, 6242-6245
1555478 CIFC23 H21 N OP 1 21/c 112.2975; 14.2131; 10.3046
90; 107.61; 90		1716.7Taguchi, Masamitsu; Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki
Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group.
Organic letters, 2015, 17, 6250-6253
1555479 CIFC24 H8 Br2 N2P 1 21/n 111.5512; 7.5173; 22.879
90; 91.554; 90		1985.9Min, Lijun; Pan, Bin; Gu, Yanlong
Synthesis of Quinoline-Fused 1-Benzazepines through a Mannich-Type Reaction of a C,N-Bisnucleophile Generated from 2-Aminobenzaldehyde and 2-Methylindole.
Organic letters, 2016, 18, 364-367
1555480 CIFC21 H18 Br NP 1 21 110.094; 14.285; 11.689
90; 90.952; 90		1685.2Zhang, Zhenhua; Du, Haifeng
Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines.
Organic letters, 2015, 17, 6266-6269
1555481 CIFC24 H24 N2 O2P 1 21/c 19.0073; 29.18; 7.8919
90; 104.587; 90		2007.39Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.
Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.
Organic letters, 2015, 17, 6270-6273
1555482 CIFC24 H24 N2 OP -110.369; 13.94; 14.494
83.533; 85.279; 75.051		2008.1Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.
Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.
Organic letters, 2015, 17, 6270-6273
1555483 CIFC25 H30 N2 O5P 1 21 18.73; 13.8357; 9.1173
90; 93.75; 90		1098.88Zhang, Hua; Zhu, Kong-Kai; Han, Ying-Shan; Luo, Cheng; Wainberg, Mark A.; Yue, Jian-Min
Flueggether A and Virosinine A, Anti-HIV Alkaloids from Flueggea virosa.
Organic letters, 2015, 17, 6274-6277
1555484 CIFC16 H24 N3 O3 PP b c a28.26; 11.505; 11.128
90; 90; 90		3618Ahamad, Shakir; Kant, Ruchir; Mohanan, Kishor
Metal-Free Three-Component Domino Approach to Phosphonylated Triazolines and Triazoles.
Organic letters, 2016, 18, 280-283
1555485 CIFC22 H13 Cl F N3 O SP n a 2117.7894; 18.2676; 5.7336
90; 90; 90		1863.2Fan, Wei; Li, Qun; Li, Yanrong; Sun, Hao; Jiang, Bo; Li, Guigen
I2/O2-Enabled N-S Bond Formation to Access Functionalized 1,2,3-Thiadiazoles.
Organic letters, 2016, 18, 1258-1261
1555486 CIFC25 H19.78 N3 O2.39 PdP -18.4976; 11.7441; 20.5928
80.687; 83.765; 78.031		1977.91Wiest, Johannes M.; Pöthig, Alexander; Bach, Thorsten
Pyrrole as a Directing Group: Regioselective Pd(II)-Catalyzed Alkylation and Benzylation at the Benzene Core of 2-Phenylpyrroles.
Organic letters, 2016, 18, 852-855
1555487 CIFC20 H21 N O2P b c a14.6593; 7.8044; 27.406
90; 90; 90		3135.4Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555488 CIFC17 H17 N O SP 1 21/c 18.6142; 9.0565; 18.42
90; 103.352; 90		1398.18Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555489 CIFC15 H17 N OP 1 21/n 114.5023; 8.2306; 20.0369
90; 98.744; 90		2363.9Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555490 CIFC19 H19 N OP b c a13.21; 7.8624; 27.4014
90; 90; 90		2846Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555491 CIFC23 H29 N O4 SP -19.523; 9.6405; 11.7824
83.18; 76.85; 71.05		995.1Murai, Kenichi; Matsuura, Kei; Aoyama, Hiroshi; Fujioka, Hiromichi
Oxidative Rearrangement via in Situ Generated N-Chloroamine: Synthesis of Fused Tetrahydroisoquinolines.
Organic letters, 2016, 18, 1314-1317
1555492 CIFC16 H17 N3 O3P -18.6512; 13.1178; 13.2085
94.755; 97.921; 102.375		1440.34Zhang, Lin-Bao; Zhang, Shou-Kun; Wei, Donghui; Zhu, Xinju; Hao, Xin-Qi; Su, Jian-Hang; Niu, Jun-Long; Song, Mao-Ping
Cobalt(II)-Catalyzed C-H Amination of Arenes with Simple Alkylamines.
Organic letters, 2016, 18, 1318-1321
1555493 CIFC17 H21 NP -16.0723; 8.6709; 14.006
75.45; 78.72; 70.16		666.5Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555494 CIFC19 H33 N O6P 1 21/c 119.714; 6.3466; 16.045
90; 90.8; 90		2007.3Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555495 CIFC24 H22 Br N3 O5.5P 21 21 2112.8376; 12.9227; 14.0967
90; 90; 90		2338.59Kumarswamyreddy, Nandarapu; Kesavan, Venkitasamy
Enantioselective Synthesis of Dihydrospiro[indoline-3,4'-pyrano[2,3-c]pyrazole] Derivatives via Michael/Hemiketalization Reaction.
Organic letters, 2016, 18, 1354-1357
1555496 CIFC25 H22 F N O2P 21 21 219.56524; 18.64102; 22.57118
90; 90; 90		4024.57Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555497 CIFC25 H22 Cl N O2P 1 21 110.8203; 8.0501; 11.8593
90; 90.3984; 90		1032.97Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555498 CIFC88 H89 B3 N6P 1 21/n 19.8983; 28.293; 24.5786
90; 96.552; 90		6838.3Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555499 CIFC45 H51 B3 F6 N6P 1 21/n 116.672; 6.7638; 37.518
90; 99.692; 90		4170.4Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555500 CIFC19 H26 O3P 21 21 216.43415; 13.9695; 18.8234
90; 90; 90		1691.88Lin, Han; Xiao, Li-Jun; Zhou, Min-Jie; Yu, Hong-Ming; Xie, Jian-Hua; Zhou, Qi-Lin
Enantioselective Approach to (-)-Hamigeran B and (-)-4-Bromohamigeran B via Catalytic Asymmetric Hydrogenation of Racemic Ketone To Assemble the Chiral Core Framework.
Organic letters, 2016, 18, 1434-1437
1555501 CIFC20 H20 O7P 1 21/c 113.364; 7.917; 21.513
90; 127.54; 90		1804.8More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555502 CIFC21 H24 O6P 1 21/c 111.9383; 10.2634; 15.2907
90; 97.621; 90		1857More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555503 CIFC11 H12 O3P -17.2646; 8.0955; 8.184
90.831; 97.639; 93.425		476.06More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555504 CIFC33 H37 Cl N2 O6C 1 2/c 125.162; 15.406; 16.174
90; 109.269; 90		5919Di Maso, Michael J.; Nepomuceno, Gabriella M.; St Peter, Michael A.; Gitre, Haley H.; Martin, Kevin S.; Shaw, Jared T.
Synthesis of (±)-Bisavenanthramide B-6 by an Anionic Anhydride Mannich Reaction.
Organic letters, 2016, 18, 1740-1743
1555505 CIFC164 H260 N4 O75 S3P 21 21 2118.0825; 18.5554; 56.7015
90; 90; 90		19024.9Inouye, Masahiko; Yoshizawa, Atsushi; Shibata, Mari; Yonenaga, Yuki; Fujimoto, Kazuhisa; Sakata, Takuma; Matsumoto, Shinya; Shiro, Motoo
Cyclodextrin-Isolated Alkynylpyrenes as UV-Stable and Blue-Light-Emitting Molecules Even in Condensed States.
Organic letters, 2016, 18, 1960-1963
1555506 CIFC26 H36 O3P 1 21 110.2913; 7.9908; 13.7239
90; 97.986; 90		1117.65Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555507 CIFC26 H38 O3P 1 21 110.3364; 8.2959; 12.9455
90; 96.995; 90		1101.81Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555508 CIFC18 H21 N O5P 1 21/n 112.4616; 7.5556; 17.8282
90; 109.236; 90		1584.9Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555509 CIFC17 H18 Cl N O5P 21 21 216.891; 11.883; 20.413
90; 90; 90		1671.5Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555510 CIFC23 H23 N O5P 1 21/n 116.5186; 6.7973; 17.4934
90; 97.222; 90		1948.6Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555511 CIFC17 H19 N O5P 21 21 217.7825; 12.1682; 16.9656
90; 90; 90		1606.63Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555512 CIFC26 H22 N3 O2 PP 1 21/c 111.3945; 16.435; 12.4553
90; 107.236; 90		2227.7Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555513 CIFC26 H22 N3 O2 PP 1 21/c 110.704; 21.3272; 11.2625
90; 120.672; 90		2211.4Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555514 CIFC21 H28 O4P 1 21/c 115.5552; 15.6415; 8.1031
90; 94.596; 90		1965.2Elliott, Daniel C.; Ma, Tsz-Kan; Selmani, Aymane; Cookson, Rosa; Parsons, Philip J.; Barrett, Anthony G. M.
Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates.
Organic letters, 2016, 18, 1800-1803
1555515 CIFC19 H16 Cl N O2P 1 21/c 112.568; 7.479; 17.461
90; 108.353; 90		1557.8Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555516 CIFC19 H17 N O2P -18.206; 8.581; 10.584
90.785; 100.066; 104.431		709.4Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555517 CIFC15 H16 O3R -3 :H29.475; 29.475; 7.245
90; 90; 120		5451Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555518 CIFC18 H22 O5P 1 21/n 16.613; 28.29; 8.886
90; 103.404; 90		1617.1Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555519 CIFC13 H15 Br Cl N O2P 1 21/c 110.4382; 24.2507; 10.9589
90; 95.0262; 90		2763.4Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555520 CIFC9 H7 Cl N2P 1 21/c 19.8146; 3.9248; 20.553
90; 103.021; 90		771.35Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555521 CIFC23 H16 F2 N4 O2P 1 21 17.8577; 14.9042; 9.3787
90; 113.529; 90		1007.05Qiao, Jin-Bao; Zhao, Yu-Ming; Gu, Peiming
Asymmetric Intramolecular Desymmetrization of meso-α,α'-Diazido Alcohols with Aryldiazoacetates: Assembly of Chiral C3 Fragments with Three Continuous Stereocenters.
Organic letters, 2016, 18, 1984-1987
1555522 CIFC15 H21 N3 O3P -16.433; 7.542; 15.771
90.874; 95.675; 109.593		716.4Mehr, S Hessam M; Patrick, Brian O.; MacLachlan, Mark J.
Stabilization of a Strained Heteroradialene by Peripheral Electron Delocalization.
Organic letters, 2016, 18, 1840-1843
1555523 CIFC17 H25 Cl F N OP 1 21/c 113.3762; 9.6596; 13.4588
90; 93.8818; 90		1735.01Hamel, Jean-Denys; Cloutier, Mélissa; Paquin, Jean-François
Exploiting a Difference in Leaving Group Ability: An Approach to β-Substituted Monofluoroalkenes Using gem-Chlorofluoropropenes.
Organic letters, 2016, 18, 1852-1855
1555524 CIFC20 H14P 1 21 16.4855; 7.5481; 13.9074
90; 95.824; 90		677.3Zhou, Yujing; Ye, Fei; Zhou, Qi; Zhang, Yan; Wang, Jianbo
Cu(I)-Catalyzed Tandem Reaction of Carbene Coupling and Horner-Wadsworth-Emmons Type Olefination: Access toward Enynes.
Organic letters, 2016, 18, 2024-2027
1555525 CIFC23 H39 N O3 S SiP 21 21 2111.2183; 17.958; 25.733
90; 90; 90		5184.1Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555526 CIFC25 H37 N3 O3P 21 21 218.174; 12.797; 21.823
90; 90; 90		2282.7Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555527 CIFC21 H33 N O5P 21 21 211.42; 19.1624; 9.3685
90; 90; 90		2050.2Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555528 CIFC18 H31 N O5P 21 21 217.71375; 8.88494; 28.0459
90; 90; 90		1922.16Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555529 CIFC21 H31 N O5P 1 21 111.5555; 6.7668; 12.9264
90; 98.846; 90		998.74Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555530 CIFC38 H22P 1 21/n 117.4392; 7.3355; 17.5242
90; 94.296; 90		2235.49Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555531 CIFC36 H18P 1 21/c 112.7866; 3.9237; 42.438
90; 95.156; 90		2120.53Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555532 CIFC15 H11 Br N2 OP 1 21/c 17.5865; 11.136; 15.609
90; 96.63; 90		1309.9Wang, Jie; Zha, Shanke; Chen, Kehao; Zhang, Feifei; Song, Chao; Zhu, Jin
Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C-H Functionalization of Benzimidates with Dioxazolones.
Organic letters, 2016, 18, 2062-2065
1555533 CIFC20 H20 O2 S2P 1 21/n 110.3493; 16.6118; 11.4274
90; 116.111; 90		1764.1Lai, Junshan; Liang, Yongping; Liu, Teng; Tang, Shouchu
Dithiane Induced Cycloaddition/Aromatization Tactic for the Synthesis of Multisubstituted Furans.
Organic letters, 2016, 18, 2066-2069
1555534 CIFC20 H28 N2 O3P 1 21 19.7442; 6.1717; 14.9524
90; 90.609; 90		899.16Hsieh, Sheng-Ying; Bode, Jeffrey W.
Silicon Amine Reagents for the Photocatalytic Synthesis of Piperazines from Aldehydes and Ketones.
Organic letters, 2016, 18, 2098-2101
1555535 CIFC19 H25 Cl N O RhP 1 21/c 113.0578; 15.8566; 18.5108
90; 91.055; 90		3832.1Wang, Qiang; Li, Xingwei
Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis.
Organic letters, 2016, 18, 2102-2105
1555536 CIFC15 H15 Br O3 SP 1 21 15.92604; 12.2676; 9.9444
90; 103.755; 90		702.21Pagire, Santosh K.; Paria, Suva; Reiser, Oliver
Synthesis of β-Hydroxysulfones from Sulfonyl Chlorides and Alkenes Utilizing Visible Light Photocatalytic Sequences.
Organic letters, 2016, 18, 2106-2109
1555537 CIFC46 H39 Au2 F6 N O5 P2 S3P 1 c 114.011; 16.7528; 20.7802
90; 105.001; 90		4711.4Tamai, Taichi; Fujiwara, Keiko; Higashimae, Shinya; Nomoto, Akihiro; Ogawa, Akiya
Gold-Catalyzed Anti-Markovnikov Selective Hydrothiolation of Unactivated Alkenes.
Organic letters, 2016, 18, 2114-2117
1555538 CIFC12 H13 N O2P 1 21/n 19.8079; 8.8394; 12.567
90; 99.596; 90		1074.3Fraboni, Americo J.; Brenner-Moyer, Stacey E
Dienamine-Catalyzed Nitrone Formation via Redox Reaction.
Organic letters, 2016, 18, 2146-2149
1555539 CIFC16 H15 Br Cl3 N O2P -17.5091; 10.1225; 12.5419
76.957; 81.066; 75.302		893.46García-García, Carolina; Ortiz-Rojano, Laura; Álvarez, Susana; Álvarez, Rosana; Ribagorda, María; Carreño, M Carmen
Friedel-Crafts Alkylation of Indoles with p-Quinols: The Role of Hydrogen Bonding of Water for the Desymmetrization of the Cyclohexadienone System.
Organic letters, 2016, 18, 2224-2227
1555540 CIFC17 H11 N OP -13.991; 10.967; 15.118
73.536; 86.417; 81.507		627.5Wang, Lianjie; Liu, Xiaocui; Wang, Mang; Liu, Jun
Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans.
Organic letters, 2016, 18, 2162-2165
1555541 CIFC20 H27 O3.5I 4119.7536; 19.7536; 9.0366
90; 90; 90		3526.1Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555542 CIFC20 H26 O3P 21 21 219.7169; 10.1381; 17.5286
90; 90; 90		1726.76Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555543 CIFC22 H32 O4C 1 2 118.2916; 8.7712; 12.993
90; 103.232; 90		2029.24Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555544 CIFC22 H20 Br N O2P 1 21 18.6651; 5.8524; 18.9495
90; 93.712; 90		958.94Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555545 CIFC24 H25 N O4P 112.7971; 12.8656; 14.0933
88.968; 86.108; 66.582		2124.21Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555546 CIFC28 H25 N O2P 21 21 215.9977; 8.669; 42.0392
90; 90; 90		2185.79Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555547 CIFC40 H40 N2 O SP -110.2707; 12.5581; 14.2615
78.265; 69.761; 81.577		1684Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555548 CIFC26 H25 Cl2 N O4 SP -19.9795; 10.2314; 12.8722
92.489; 106.194; 96.538		1250.1Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555549 CIFC21 H15 NP -110.3062; 11.6276; 13.2088
75.92; 88.72; 87.09		1533.28Saunthwal, Rakesh K.; Patel, Monika; Verma, Akhilesh K.
Metal- and Protection-Free [4 + 2] Cycloadditions of Alkynes with Azadienes: Assembly of Functionalized Quinolines.
Organic letters, 2016, 18, 2200-2203
1555550 CIFC12 H9 F3 N2 OP 1 21/c 19.3458; 13.3878; 9.015
90; 104.592; 90		1091.57Nguyen, Thanh Binh; Ermolenko, Ludmila; Retailleau, Pascal; Al-Mourabit, Ali
Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2016, 18, 2177-2179
1555551 CIFC16 H18 N2 O2P 1 21 18.94706; 11.2291; 14.9983
90; 102.552; 90		1470.83Halskov, Kim Søholm; Næsborg, Line; Tur, Fernando; Jørgensen, Karl Anker
Asymmetric [3 + 2] Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Aldehydes by Synergistic Palladium and Organocatalysis.
Organic letters, 2016, 18, 2220-2223
1555552 CIFC8 H9 Cl N4 OP 21 21 215.3345; 17.4841; 6.9026
90; 90; 90		1850.7Sun, Huan-Li; Chen, Fei; Xie, Ming-Sheng; Guo, Hai-Ming; Qu, Gui-Rong; He, Yan-Mei; Fan, Qing-Hua
Asymmetric Hydrogenation of α-Purine Nucleobase-Substituted Acrylates with Rhodium Diphosphine Complexes: Access to Tenofovir Analogues.
Organic letters, 2016, 18, 2260-2263
1555553 CIFC18 H22 F N O4P 21 21 219.7821; 11.5835; 14.8591
90; 90; 90		1683.7Zhu, Luyi; Chen, Qiliang; Shen, Dan; Zhang, Weihao; Shen, Cong; Zeng, Xiaofei; Zhong, Guofu
Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction.
Organic letters, 2016, 18, 2387-2390
1555554 CIFC28 H24 O6 S2P 1 21/c 116.268; 7.4469; 22.374
90; 110.413; 90		2540.3Ni, Chunjie; Wang, MingLi; Tong, Xiaofeng
Access to Thiophene and 1H-Pyrrole via Amine-Initiated (3 + 2) Annulation and Aromatization Cascade Reaction of β'-Acetoxy Allenoate and 1,2-Bisnucleophile.
Organic letters, 2016, 18, 2240-2243
1555555 CIFC33 H26 Cl N O5 SP 1 21/c 110.2049; 23.693; 12.5597
90; 107.704; 90		2892.9Lv, Leiyang; Li, Zhiping
Iron-Catalyzed Radical [2 + 2 + 2] Annulation of Benzene-Linked 1,7-Enynes with Aldehydes: Fused Pyran Compounds.
Organic letters, 2016, 18, 2264-2267
1555556 CIFC22 H18 Br2 O4P 1 21/n 18.4295; 10.9126; 22.07
90; 90.7067; 90		2030.02Li, Shuangjiang; Huang, Changfeng; Thakellapalli, Haresh; Farajidizaji, Behzad; Popp, Brian V.; Petersen, Jeffrey L.; Wang, Kung K.
Syntheses and Structures of Functionalized [9]Cycloparaphenylenes as Carbon Nanohoops Bearing Carbomethoxy and N-Phenylphthalimido Groups.
Organic letters, 2016, 18, 2268-2271
1555557 CIFC91 H80 Cl2 O12P -114.0233; 16.2794; 19.2082
66.9176; 72.0505; 77.5633		3815.2Li, Shuangjiang; Huang, Changfeng; Thakellapalli, Haresh; Farajidizaji, Behzad; Popp, Brian V.; Petersen, Jeffrey L.; Wang, Kung K.
Syntheses and Structures of Functionalized [9]Cycloparaphenylenes as Carbon Nanohoops Bearing Carbomethoxy and N-Phenylphthalimido Groups.
Organic letters, 2016, 18, 2268-2271
1555558 CIFC24 H20 O2P 1 21/c 111.2926; 12.6823; 13.3977
90; 112.956; 90		1766.8Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Correction to "Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides".
Organic letters, 2016, 18, 2323-2324
1555559 CIFC29 H24 O3P 1 21/c 113.3405; 7.7448; 22.406
90; 104.615; 90		2240.1Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Correction to "Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides".
Organic letters, 2016, 18, 2323-2324
1555560 CIFC14 H8 F2 N2 O SP -15.737; 7.6865; 13.5874
88.575; 86.523; 88.004		597.55Castanheiro, Thomas; Suffert, Jean; Gulea, Mihaela; Donnard, Morgan
Aerobic Copper-Mediated Domino Three-Component Approach to 2-Aminobenzothiazole Derivatives.
Organic letters, 2016, 18, 2588-2591
1555561 CIFC20 H17 Br N2 O2P -17.7454; 10.3627; 11.1019
107.48; 90.474; 97.723		841.1Liang, Ling; Huang, You
Phosphine-Catalyzed [3 + 3]-Domino Cycloaddition of Ynones and Azomethine Imines To Construct Functionalized Hydropyridazine Derivatives.
Organic letters, 2016, 18, 2604-2607
1555562 CIFC23 H30 F2 N2 O2P 1 21/n 113.5393; 9.9243; 17.0947
90; 103.566; 90		2232.9Wang, Qiang; He, Yu-Tao; Zhao, Jia-Hui; Qiu, Yi-Feng; Zheng, Lan; Hu, Jing-Yuan; Yang, Yu-Chen; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Regioselective Difluoroalkylation and Carbonylation of Alkynes.
Organic letters, 2016, 18, 2664-2667
1555563 CIFC20 H15 Cl2 N O4 SP 1 21/c 115.368; 8.0607; 16.717
90; 114.31; 90		1887.2Jia, Penghao; Huang, You
Sequential Annulation Domino Reaction of Sulfur Ylides and α,β-Unsaturated Cyclic Ketimines: Synthesis of Cyclic 2-Alkenyl Aziridines.
Organic letters, 2016, 18, 2475-2478
1555564 CIFC16 H24 N2 O3 SP 21 21 218.6938; 9.8115; 18.943
90; 90; 90		1615.8Crossley, Steven W. M.; Martinez, Ruben M.; Guevara-Zuluaga, Sebastián; Shenvi, Ryan A.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Organic letters, 2016, 18, 2620-2623
1555565 CIFC21 H22 N2 O6P -17.7666; 15.5767; 16.2634
91.394; 99.881; 90.214		1937.69Crossley, Steven W. M.; Martinez, Ruben M.; Guevara-Zuluaga, Sebastián; Shenvi, Ryan A.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Organic letters, 2016, 18, 2620-2623
1555566 CIFC37 H36 F N O5 S2P -18.6308; 13.95; 15.866
102.47; 103.64; 105.496		1707.7Guang, Jie; Rout, Saroj; Bihani, Manisha; Larson, Ariel J.; Arman, Hadi D.; Zhao, John C.-G.
Organocatalyzed Enantioselective Direct Mannich Reaction of α-Styrylacetates.
Organic letters, 2016, 18, 2648-2651
1555567 CIFC20 H17 F5 N2 O5P 1 21/c 15.76; 42.882; 8.034
90; 94.022; 90		1979.5Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555568 CIFC17 H26 N2 O2P 1 21/n 113.2033; 7.3109; 17.144
90; 97.707; 90		1639.9Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555569 CIFC13 H15 Cl F5 N O2P 1 21/n 114.84; 6.9273; 15.2459
90; 109.128; 90		1480.8Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555570 CIFC24 H19 Br N2 O2P 1 21 111.311; 5.661; 16.455
90; 108.595; 90		998.6Winterton, Sarah E.; Ready, Joseph M.
[3 + 2]-Cycloadditions of Azomethine Imines and Ynolates.
Organic letters, 2016, 18, 2608-2611
1555571 CIFC24 H35 N O5P 15.9846; 7.913; 12.691
99.814; 95.953; 107.509		557Nagaraju, Karre; Chegondi, Rambabu; Chandrasekhar, Srivari
Expanding Diversity without Protecting Groups: (+)-Sclareolide to Indolosesquiterpene Alkaloid Mycoleptodiscin A and Analogues.
Organic letters, 2016, 18, 2684-2687
1555572 CIFC25 H34 N2 O4P 21 21 216.0956; 15.5691; 24.6358
90; 90; 90		2338.01Nagaraju, Karre; Chegondi, Rambabu; Chandrasekhar, Srivari
Expanding Diversity without Protecting Groups: (+)-Sclareolide to Indolosesquiterpene Alkaloid Mycoleptodiscin A and Analogues.
Organic letters, 2016, 18, 2684-2687
1555573 CIFC23 H21 B N2 O2P 1 21/n 111.7488; 11.331; 16.0382
90; 110.789; 90		1996.09Mazzanti, Andrea; Mercanti, Elia; Mancinelli, Michele
Axial Chirality about Boron-Carbon Bond: Atropisomeric Azaborines.
Organic letters, 2016, 18, 2692-2695
1555574 CIFC27 H38 O3P -110.004; 10.563; 12.631
94.414; 111.883; 93.763		1228.5Shen, Yangyong; Qi, Jifeng; Mao, Zhenjun; Cui, Sunliang
Fe-Catalyzed Hydroalkylation of Olefins with para-Quinone Methides.
Organic letters, 2016, 18, 2722-2725
1555575 CIFC16 H15 F3 N2P 21 21 216.37164; 8.13751; 26.6535
90; 90; 90		1381.96Ma, Wenpeng; Chen, Fei; Liu, Youran; He, Yan-Mei; Fan, Qing-Hua
Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives.
Organic letters, 2016, 18, 2730-2733
1555576 CIFC27 H24 N2 O2 SP 1 21 110.581; 9.532; 11.106
90; 90.577; 90		1120.1Ma, Wenpeng; Chen, Fei; Liu, Youran; He, Yan-Mei; Fan, Qing-Hua
Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives.
Organic letters, 2016, 18, 2730-2733
1555577 CIFC18 H17 N O3P -19.2442; 9.4365; 10.1285
109.029; 92.163; 110.061		773.37Li, Chao; Jiang, Kun; Ouyang, Qin; Liu, Tian-Yu; Chen, Ying-Chun
[3 + 1]- and [3 + 2]-Cycloadditions of Azaoxyallyl Cations and Sulfur Ylides.
Organic letters, 2016, 18, 2738-2741
1555578 CIFC24 H19 N0.25 O3P c a 2120.6513; 5.9284; 14.7885
90; 90; 90		1810.5Li, Chao; Jiang, Kun; Ouyang, Qin; Liu, Tian-Yu; Chen, Ying-Chun
[3 + 1]- and [3 + 2]-Cycloadditions of Azaoxyallyl Cations and Sulfur Ylides.
Organic letters, 2016, 18, 2738-2741
1555579 CIFC49 H42 B Cl3 F2 N2 O4P -111.661; 12.035; 17.572
102.313; 101.456; 102.201		2276.9Gobo, Yuki; Yamamura, Masaki; Nakamura, Takashi; Nabeshima, Tatsuya
Synthesis and Chiroptical Properties of a Ring-Fused BODIPY with a Skewed Chiral π Skeleton.
Organic letters, 2016, 18, 2719-2721
1555580 CIFC48 H41 B F2 N2 O4C 1 2/c 119.489; 25.41; 16.809
90; 100.702; 90		8179Gobo, Yuki; Yamamura, Masaki; Nakamura, Takashi; Nabeshima, Tatsuya
Synthesis and Chiroptical Properties of a Ring-Fused BODIPY with a Skewed Chiral π Skeleton.
Organic letters, 2016, 18, 2719-2721
1555581 CIFC21 H33 N O2 SiP 1 21/n 116.5088; 8.4395; 16.9774
90; 109.4; 90		2231.1Boobalan, Ramadoss; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Ruthenium-Catalyzed C-H Alkynylation of Aromatic Amides with Hypervalent Iodine-Alkyne Reagents.
Organic letters, 2016, 18, 3314-3317
1555582 CIFC19 H28 Cl N O2 SiP 1 21/c 118.781; 13.854; 8.134
90; 93.886; 90		2111.5Boobalan, Ramadoss; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Ruthenium-Catalyzed C-H Alkynylation of Aromatic Amides with Hypervalent Iodine-Alkyne Reagents.
Organic letters, 2016, 18, 3314-3317
1555583 CIFC43 H47 N3 O5P 1 21 18.9792; 16.193; 13.2363
90; 106.625; 90		1844.1Gorske, Benjamin C.; Mumford, Emily M.; Conry, Rebecca R.
Tandem Incorporation of Enantiomeric Residues Engenders Discrete Peptoid Structures.
Organic letters, 2016, 18, 2780-2783
1555584 CIFC49 H55 N3 O6P 1 21 112.9668; 13.1573; 13.5181
90; 109.297; 90		2176.7Gorske, Benjamin C.; Mumford, Emily M.; Conry, Rebecca R.
Tandem Incorporation of Enantiomeric Residues Engenders Discrete Peptoid Structures.
Organic letters, 2016, 18, 2780-2783
1555585 CIFC15 H23 N O2 SP 21 21 216.5067; 10.2546; 22.3875
90; 90; 90		1493.77Kubiak, 2nd, Robert W; Mighion, Jeffrey D.; Wilkerson-Hill, Sidney M; Alford, Joshua S.; Yoshidomi, Tetsushi; Davies, Huw M. L.
Enantioselective Intermolecular C-H Functionalization of Allylic and Benzylic sp(3) C-H Bonds Using N-Sulfonyl-1,2,3-triazoles.
Organic letters, 2016, 18, 3118-3121
1555586 CIFC26 H26 Br N O5P -19.8599; 11.9104; 11.9139
61.836; 72.739; 86.003		1173.79Das, Saikat; Chakrabarty, Shyamal; Daniliuc, Constantin G.; Studer, Armido
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor-Acceptor Cyclopropanes with Nitrosoarenes.
Organic letters, 2016, 18, 2784-2787
1555587 CIFC22 H24 Br N O5P 21 21 218.662; 9.2342; 26.0487
90; 90; 90		2083.55Das, Saikat; Chakrabarty, Shyamal; Daniliuc, Constantin G.; Studer, Armido
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor-Acceptor Cyclopropanes with Nitrosoarenes.
Organic letters, 2016, 18, 2784-2787
1555588 CIFC53.59 H49.59 Cl1.77 Cu N6 O2P -18.0804; 16.5626; 17.4337
82.85; 78.821; 77.371		2225.3Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555589 CIFC54 H52 Cl3 Cu N6P 1 21/c 112.031; 30.509; 13.9111
90; 113.596; 90		4679.2Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555590 CIFC55.5 H50.5 Cl4.5 Cu N6C 1 2/c 125.4929; 11.6131; 33.0447
90; 98.807; 90		9667.6Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555591 CIFC45 H52 Cl2 O12 P2P 1 21 113.3931; 9.5262; 17.8614
90; 101.589; 90		2232.4Durantie, Estelle; Huwiler, Samuel; Leroux, Jean-Christophe; Castagner, Bastien
A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates.
Organic letters, 2016, 18, 3162-3165
1555592 CIFC66 H66 O12 P2P 111.2057; 15.2204; 18.506
71.165; 81.596; 89.993		2951.5Durantie, Estelle; Huwiler, Samuel; Leroux, Jean-Christophe; Castagner, Bastien
A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates.
Organic letters, 2016, 18, 3162-3165
1555593 CIFC27 H36 F3 N O3 S2 SiP -17.1867; 11.58; 17.91
87.008; 85.211; 87.346		1482Karmakar, Rajdip; Mamidipalli, Phani; Salzman, Ryan M.; Hong, Seongwon; Yun, Sang Young; Guo, Wei; Xia, Yuanzhi; Lee, Daesung
Benzannulation of Triynes Initiated by an Alder-Ene Reaction and Subsequent Trifluoromethylthiolate Addition.
Organic letters, 2016, 18, 3530-3533
1555594 CIFC27 H21 N OP 1 21 110.7656; 8.6732; 11.0548
90; 95.097; 90		1028.13Cioc, Răzvan C; Schuckman, Peter; Preschel, Hans D.; Vlaar, Tjøstil; Ruijter, Eelco; Orru, Romano V. A.
Brønsted Acid-Catalyzed Cyanotritylation of Aldehydes by Trityl Isocyanide.
Organic letters, 2016, 18, 3562-3565
1555595 CIFC24 H21 Cl F3 N O4C 1 2/c 126.236; 8.1806; 21.79
90; 100.102; 90		4604.2Zhu, Yuanyuan; Dong, Zhenghao; Cheng, Xin; Zhong, Xiaoling; Liu, Xiaolin; Lin, Li; Shen, Zhiqiang; Yang, Peiju; Li, Yuan; Wang, Hailin; Yan, Wenjin; Wang, Kairong; Wang, Rui
Asymmetric Synthesis of CF3- and Indole-Containing Thiochromanes via a Squaramide-Catalyzed Michael-Aldol Reaction.
Organic letters, 2016, 18, 3546-3549
1555596 CIFC31 H27 Cl F3 N O5 SP 1 21 110.4656; 10.4575; 26.8799
90; 89.999; 90		2941.84Zhu, Yuanyuan; Dong, Zhenghao; Cheng, Xin; Zhong, Xiaoling; Liu, Xiaolin; Lin, Li; Shen, Zhiqiang; Yang, Peiju; Li, Yuan; Wang, Hailin; Yan, Wenjin; Wang, Kairong; Wang, Rui
Asymmetric Synthesis of CF3- and Indole-Containing Thiochromanes via a Squaramide-Catalyzed Michael-Aldol Reaction.
Organic letters, 2016, 18, 3546-3549
1555597 CIFC30 H38 O5P 1 21/n 123.324; 9.264; 26.981
90; 105.014; 90		5631Yuan, Zhenbo; Wei, Weiwei; Lin, Aijun; Yao, Hequan
Bifunctional Organo/Metal Cooperatively Catalyzed [3 + 2] Annulation of para-Quinone Methides with Vinylcyclopropanes: Approach to Spiro[4.5]deca-6,9-diene-8-ones.
Organic letters, 2016, 18, 3370-3373
1555598 CIFC19 H20 N2 O1.76R 3 :H24.3768; 24.3768; 7.2197
90; 90; 120		3715.4Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555599 CIFC19 H20 N2 OP 21 21 216.8328; 11.6515; 19.2975
90; 90; 90		1536.32Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555600 CIFC19 H21 I N2 OP 1 21 17.272; 9.1963; 13.4788
90; 101.735; 90		882.6Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555601 CIFC19 H20 N2 OP 1 21 110.3077; 7.8255; 10.6948
90; 117.859; 90		762.69Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555602 CIFC41 H39 N3 O4 S2C 1 2/c 138.8089; 9.9944; 20.8313
90; 111.915; 90		7496Zhang, Jingyi; Zhang, Qingshuang; Xia, Biao; Wu, Jie; Wang, Xiao-Na; Chang, Junbiao
Metal-Free [2 + 2 + 2] Cycloaddition of Ynamides with Nitriles to Construct 2,4-Diaminopyridines.
Organic letters, 2016, 18, 3390-3393
1555603 CIFC20 H16 N4 O2P 1 21/c 16.1927; 35.576; 8.386
90; 106.723; 90		1769.4Shelke, Anil M.; Suryavanshi, Gurunath
Fluoride-Assisted Synthesis of 1,4,5,6-Tetrahydropyridazines via [4 + 2] Cyclodimerization of in Situ-Generated Azoalkenes Followed by a C-N Bond Cleavage.
Organic letters, 2016, 18, 3968-3971
1555604 CIFC82 H63 Cl6 N15 O3P 1 21/n 116.103; 13.8295; 31.954
90; 92.721; 90		7108Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555605 CIFC76 H59 Cl4 N15 O3P 1 21/n 117.7889; 21.013; 37.032
90; 102.091; 90		13535Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555606 CIFC61.5 H54 Cl7.5 N15 O3P 1 21/c 110.7001; 20.2403; 29.729
90; 91.17; 90		6437.2Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555607 CIFC73 H52 Cl9.01 N15 O3P 1 21/n 116.133; 13.761; 32.115
90; 92.117; 90		7125Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555608 CIFC74 H55 Cl2 N15 O3P 1 21/c 121.861; 15.4737; 18.6
90; 98.075; 90		6229.4Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555609 CIFC75.47 H59 Cl2.36 N15 O3P 1 21/c 110.7998; 20.2414; 29.845
90; 91.909; 90		6520.6Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555610 CIFC74 H61 Cl6 N15 O3P 1 21/n 116.154; 13.571; 31.638
90; 90.061; 90		6936Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555611 CIFC80 H63 Cl6 N15 O3P 1 21/n 116.218; 13.8125; 31.653
90; 92.288; 90		7085Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555612 CIFC80 H63 Cl6 N15 O3P 1 21/n 116.1736; 13.7072; 31.887
90; 92.389; 90		7063Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555613 CIFC56.75 H41.75 Cl8.25 N15 O3P -110.11; 21.965; 27.902
99.418; 94.933; 90.93		6087Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555614 CIFC75 H54 Cl9 N15 O3P 1 21/n 116.056; 13.8514; 32.082
90; 91.878; 90		7131.1Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555615 CIFC71.5 H52.5 Cl10.5 N15 O3P 1 21/n 116.42; 13.581; 32.38
90; 92.96; 90		7211Samanta, Jayanta; Natarajan, Ramalingam
Cofacial Organic Click Cage to Intercalate Polycyclic Aromatic Hydrocarbons.
Organic letters, 2016, 18, 3394-3397
1555616 CIFC49 H25 F9P 21 21 219.7462; 17.2319; 23.8323
90; 90; 90		4002.5Rao, M. Rajeswara; Johnson, Shea; Perepichka, Dmitrii F.
Aromatization of Benzannulated Perylene-3,9-diones: Unexpected Photophysical Properties and Reactivity.
Organic letters, 2016, 18, 3574-3577
1555617 CIFC26 H30 N4 O5P 21 21 219.7084; 15.1043; 16.6406
90; 90; 90		2440.2Wang, Kai-Bo; Li, Da-Hong; Hu, Ping; Wang, Wen-Jing; Lin, Clement; Wang, Jian; Lin, Bin; Bai, Jiao; Pei, Yue-Hu; Jing, Yong-Kui; Li, Zhan-Lin; Yang, Danzhou; Hua, Hui-Ming
A Series of β-Carboline Alkaloids from the Seeds of Peganum harmala Show G-Quadruplex Interactions.
Organic letters, 2016, 18, 3398-3401
1555618 CIFC6 H3 I O2P 1 21/n 19.7136; 8.3719; 16.672
90; 97.5683; 90		1343.98Jardim, Guilherme A. M.; Bower, John F.; da Silva Júnior, Eufrânio N
Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation.
Organic letters, 2016, 18, 4454-4457
1555619 CIFC7 H5 I O3P n a 218.0841; 14.9751; 6.2629
90; 90; 90		758.19Jardim, Guilherme A. M.; Bower, John F.; da Silva Júnior, Eufrânio N
Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation.
Organic letters, 2016, 18, 4454-4457
1555620 CIFC16 H10 O2 SeP 1 21/c 17.8829; 8.6055; 18.1935
90; 96.7142; 90		1225.72Jardim, Guilherme A. M.; Bower, John F.; da Silva Júnior, Eufrânio N
Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation.
Organic letters, 2016, 18, 4454-4457
1555621 CIFC26 H23 NP b c a17.814; 9.6903; 23.0455
90; 90; 90		3978.18Li, Nan; Lian, Xiao-Lei; Li, Yu-Hui; Wang, Tian-Yi; Han, Zhi-Yong; Zhang, Liming; Gong, Liu-Zhu
Gold-Catalyzed Direct Assembly of Aryl-Annulated Carbazoles from 2-Alkynyl Arylazides and Alkynes.
Organic letters, 2016, 18, 4178-4181
1555622 CIFC19 H15 N O SP 21 21 215.5711; 6.5999; 40.0657
90; 90; 90		1473.16Ahlemeyer, Nicholas A.; Birman, Vladimir B.
Asymmetric Catalytic Synthesis of Thiochromenes via an Acyl Transfer-Initiated Cascade.
Organic letters, 2016, 18, 3454-3457
1555623 CIFC24 H32 O3P 21 21 217.9418; 9.0278; 28.012
90; 90; 90		2008.4Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555624 CIFC26 H34 O4P 1 21 19.4038; 23.797; 9.9633
90; 90.656; 90		2229.5Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555625 CIFC28 H38 O8P 21 21 218.352; 14.9946; 40.87
90; 90; 90		5118.4Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555626 CIFC31 H46 O8P 21 21 217.4728; 11.6974; 33.552
90; 90; 90		2932.9Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555627 CIFC29 H40 Cl2 O8P 1 21 17.6253; 11.8707; 16.229
90; 90.932; 90		1468.8Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555628 CIFC28 H40 O7P 21 21 2113.3481; 15.278; 36.973
90; 90; 90		7540Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555629 CIFC28 H44 O9P 21 21 219.3211; 11.4032; 26.089
90; 90; 90		2773Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555630 CIFC28 H40 O9C 1 2 126.073; 7.8003; 29.094
90; 91.171; 90		5916Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555631 CIFC24 H30 O3P 1 21 16.2298; 12.745; 12.605
90; 99.799; 90		986.2Ren, Jian; Shi, Xin; Li, Xiao-Nian; Li, Lai-Wei; Su, Jia; Shao, Li-Dong; Zhao, Qin-Shi
Synthesis of a Small-Molecule Library with Skeletal Diversity from Hemslecin A via the Reaction-Discovery Strategy.
Organic letters, 2016, 18, 3948-3951
1555632 CIFC12 H13 N O3P b c a12.5299; 11.0917; 15.3671
90; 90; 90		2135.69Patzelt, Christoph; Pöthig, Alexander; Gulder, Tanja
Iodine(III)-Catalyzed Cascade Reactions Enabling a Direct Access to β-Lactams and α-Hydroxy-β-amino Acids.
Organic letters, 2016, 18, 3466-3469
1555633 CIFC33 H32 N2 O2 PtC 1 c 15.767; 26.604; 17.464
90; 96.051; 90		2664.5Saris, Patrick J. G.; Thompson, Mark E.
Gram Scale Synthesis of Benzophenanthroline and Its Blue Phosphorescent Platinum Complex.
Organic letters, 2016, 18, 3960-3963
1555634 CIFC22 H14 N2P 1 21/c 19.5057; 14.8773; 11.4295
90; 110.562; 90		1513.38Saris, Patrick J. G.; Thompson, Mark E.
Gram Scale Synthesis of Benzophenanthroline and Its Blue Phosphorescent Platinum Complex.
Organic letters, 2016, 18, 3960-3963
1555635 CIFC20 H26 N2 O2P 21 21 219.01057; 10.9727; 17.5326
90; 90; 90		1733.45Tokuda, Ryoko; Okamoto, Yoshiki; Koyama, Tetsuya; Kogure, Noriyuki; Kitajima, Mariko; Takayama, Hiromitsu
Asymmetric Total Synthesis of Kopsiyunnanine K, a Monoterpenoid Indole Alkaloid with a Rearranged Skeleton.
Organic letters, 2016, 18, 3490-3493
1555636 CIFC35 H22P 1 21/c 112.558; 14.18; 26.385
90; 102.72; 90		4583Oyama, Hiromi; Akiyama, Midori; Nakano, Koji; Naito, Masanobu; Nobusawa, Kazuyuki; Nozaki, Kyoko
Synthesis and Properties of [7]Helicene-like Compounds Fused with a Fluorene Unit.
Organic letters, 2016, 18, 3654-3657
1555637 CIFC29 H16 OP b c a13.816; 13.862; 19.248
90; 90; 90		3686.3Oyama, Hiromi; Akiyama, Midori; Nakano, Koji; Naito, Masanobu; Nobusawa, Kazuyuki; Nozaki, Kyoko
Synthesis and Properties of [7]Helicene-like Compounds Fused with a Fluorene Unit.
Organic letters, 2016, 18, 3654-3657
1555638 CIFC41 H26P 21 21 219.8499; 11.1882; 24.6237
90; 90; 90		2713.6Oyama, Hiromi; Akiyama, Midori; Nakano, Koji; Naito, Masanobu; Nobusawa, Kazuyuki; Nozaki, Kyoko
Synthesis and Properties of [7]Helicene-like Compounds Fused with a Fluorene Unit.
Organic letters, 2016, 18, 3654-3657
1555639 CIFC24 H17 N OP n a 2115.3059; 12.1881; 9.628
90; 90; 90		1796.1Chen, Si; Wu, Xin-Xing; Wang, Jia; Hao, Xin-Hua; Xia, Yu; Shen, Yi; Jing, Huanwang; Liang, Yong-Min
Palladium-Catalyzed Intramolecular Dearomatization of Indoles via Decarboxylative Alkynyl Termination.
Organic letters, 2016, 18, 4016-4019
1555640 CIFC22 H29 N2 O4.5 SP 1 21 18.0776; 24.432; 11.904
90; 108.916; 90		2222.4Lan, Xiaoyu; Tao, Chuangan; Liu, Xuliang; Zhang, Aina; Zhao, Baoguo
Asymmetric Transamination of α-Keto Acids Catalyzed by Chiral Pyridoxamines.
Organic letters, 2016, 18, 3658-3661
1555641 CIFC17 H15 F N2 O3 SP 1 21/c 111.9912; 15.1463; 9.459
90; 111.614; 90		1597.17Qian, Jing; Sheng, Guorong; Huang, Kai; Liu, Shaojie; Lu, Ping; Wang, Yanguang
α-Amidino Rhodium Carbenes: Key Intermediates for the Preparation of (E)-2-Aminomethylene-3-oxoindoles and Pyranoindoles.
Organic letters, 2016, 18, 3682-3685
1555642 CIFC20 H20 N2 O3 SP -15.5675; 8.631; 19.5676
77.417; 83.698; 82.645		906.89Qian, Jing; Sheng, Guorong; Huang, Kai; Liu, Shaojie; Lu, Ping; Wang, Yanguang
α-Amidino Rhodium Carbenes: Key Intermediates for the Preparation of (E)-2-Aminomethylene-3-oxoindoles and Pyranoindoles.
Organic letters, 2016, 18, 3682-3685
1555643 CIFC21 H18 N2 O4 SP -17.3603; 7.543; 17.2163
87.384; 86.032; 74.912		920.29Qian, Jing; Sheng, Guorong; Huang, Kai; Liu, Shaojie; Lu, Ping; Wang, Yanguang
α-Amidino Rhodium Carbenes: Key Intermediates for the Preparation of (E)-2-Aminomethylene-3-oxoindoles and Pyranoindoles.
Organic letters, 2016, 18, 3682-3685
1555644 CIFC20 H24 F4 N2 O2 ZnP 1 21/n 114.438; 8.4217; 17.3621
90; 93.541; 90		2107.07Aikawa, Kohsuke; Serizawa, Hiroki; Ishii, Koki; Mikami, Koichi
Palladium-Catalyzed Negishi Cross-Coupling Reaction of Aryl Halides with (Difluoromethyl)zinc Reagent.
Organic letters, 2016, 18, 3690-3693
1555645 CIFC28 H29 N O2P 21 21 215.0975; 10.807; 40.2707
90; 90; 90		2218.46Li, Wenbo; Yu, Xiuzhao; Yue, Zhenting; Zhang, Junliang
Asymmetric Construction of 2,3-Dihydroisoxazoles via an Organocatalytic Formal [3 + 2] Cycloaddition of Enynes with N-Hydroxylamines.
Organic letters, 2016, 18, 3972-3975
1555646 CIFC27 H22 Cl2 O6P 21 21 217.2743; 10.1737; 32.241
90; 90; 90		2386Ashtekar, Kumar Dilip; Ding, Xinliang; Toma, Edmond; Sheng, Wei; Gholami, Hadi; Rahn, Christopher; Reed, Paul; Borhan, Babak
Mechanistically Inspired Route toward Hexahydro-2H-chromenes via Consecutive [4 + 2] Cycloadditions.
Organic letters, 2016, 18, 3976-3979
1555647 CIFC31 H32 Cl4 O8P 21 21 2110.9256; 14.7077; 19.6645
90; 90; 90		3159.9Ashtekar, Kumar Dilip; Ding, Xinliang; Toma, Edmond; Sheng, Wei; Gholami, Hadi; Rahn, Christopher; Reed, Paul; Borhan, Babak
Mechanistically Inspired Route toward Hexahydro-2H-chromenes via Consecutive [4 + 2] Cycloadditions.
Organic letters, 2016, 18, 3976-3979
1555648 CIFC10 H7 B F2 N2 OC 1 c 114.246; 9.001; 14.506
90; 89.933; 90		1860Miura, Wataru; Hirano, Koji; Miura, Masahiro
Rhodium-Catalyzed C6-Selective C-H Borylation of 2-Pyridones.
Organic letters, 2016, 18, 3742-3745
1555649 CIFC16 H19 B N2 O3P -110.4857; 10.8482; 14.0338
70.4935; 89.135; 89.14		1504.5Miura, Wataru; Hirano, Koji; Miura, Masahiro
Rhodium-Catalyzed C6-Selective C-H Borylation of 2-Pyridones.
Organic letters, 2016, 18, 3742-3745
1555650 CIFC16 H12 N2 OP -18.41; 11.941; 13.209
74.04; 89.25; 85.17		1271Miura, Wataru; Hirano, Koji; Miura, Masahiro
Rhodium-Catalyzed C6-Selective C-H Borylation of 2-Pyridones.
Organic letters, 2016, 18, 3742-3745
1555651 CIFC17 H20 F N O4 SP -18.5007; 10.25; 11.2985
75.804; 70.345; 81.631		896.6Chang, Jian; Liu, Bangyu; Yang, Yang; Wang, Mang
Pd-Catalyzed C-S Activation/Isocyanide Insertion/Hydrogenation Enables a Selective Aerobic Oxidation/Cyclization.
Organic letters, 2016, 18, 3984-3987
1555652 CIFC19 H18 O5P 1 21/c 18.4205; 19.329; 10.1617
90; 103.506; 90		1608.2Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin
Transition-Metal-Free Coupling Annulation of Arynes with Ketones and Alkynoates: Assembly of Functionalized Naphthalenes.
Organic letters, 2016, 18, 3762-3765
1555653 CIFC14 H13 N3 O SP -15.6316; 8.8731; 13.3605
76.69; 87.767; 85.418		647.47Bongers, Amanda; Ranasinghe, Indee; Lemire, Philippe; Perozzo, Alyssa; Vincent-Rocan, Jean-François; Beauchemin, André M
Synthesis of Cyclic Azomethine Imines by Cycloaddition Reactions of N-Isocyanates and N-Isothiocyanates.
Organic letters, 2016, 18, 3778-3781
1555654 CIFC27 H28 O3P -19.9759; 13.6806; 17.6508
109.19; 96.4682; 98.2575		2218.3Nugent, Jeremy; Banwell, Martin G.; Schwartz, Brett D.
Total Synthesis of the Illicium-Derived Sesquineolignan Simonsol C.
Organic letters, 2016, 18, 3798-3801
1555655 CIFC36 H18C 1 c 128.619; 13.5049; 11.3279
90; 101.05; 90		4297Fujikawa, Takao; Preda, Dorin V.; Segawa, Yasutomo; Itami, Kenichiro; Scott, Lawrence T.
Corannulene-Helicene Hybrids: Chiral π-Systems Comprising Both Bowl and Helical Motifs.
Organic letters, 2016, 18, 3992-3995
1555656 CIFC16 H12 Br F3 OP 1 21/n 115.924; 5.6656; 18.306
90; 114.74; 90		1500Zhu, Chuanle; Chen, Pengquan; Wu, Wanqing; Qi, Chaorong; Ren, Yanwei; Jiang, Huanfeng
Transition-Metal-Free Diastereoselective Epoxidation of Trifluoromethylketones with N-Tosylhydrazones: Access to Tetrasubstituted Trifluoromethylated Oxiranes.
Organic letters, 2016, 18, 4008-4011
1555657 CIFC90 H188 Cd1.5 Cl4 N60 O79P 1 21/n 119.793; 22.357; 32.252
90; 92.9; 90		14254Li, Qing; Qiu, Sheng-Chao; Zhang, Jing; Chen, Kai; Huang, Ying; Xiao, Xin; Zhang, Yingjie; Li, Feng; Zhang, Yun-Qian; Xue, Sai-Feng; Zhu, Qian-Jiang; Tao, Zhu; Lindoy, Leonard F.; Wei, Gang
Twisted Cucurbit[n]urils.
Organic letters, 2016, 18, 4020-4023
1555658 CIFC156 H286 Cd7 Cl20 Dy2 N104 O133P 1 21/c 118.217; 52.952; 17.532
90; 110.13; 90		15879Li, Qing; Qiu, Sheng-Chao; Zhang, Jing; Chen, Kai; Huang, Ying; Xiao, Xin; Zhang, Yingjie; Li, Feng; Zhang, Yun-Qian; Xue, Sai-Feng; Zhu, Qian-Jiang; Tao, Zhu; Lindoy, Leonard F.; Wei, Gang
Twisted Cucurbit[n]urils.
Organic letters, 2016, 18, 4020-4023
1555659 CIFC21 H22 O7P 1 21 16.9891; 17.3736; 8.347
90; 105.219; 90		978Zhou, Jinchuan; Zhang, Jiaozhen; Li, Ruijuan; Liu, Jun; Fan, Peihong; Li, Yi; Ji, Mei; Dong, Yiwen; Yuan, Huiqing; Lou, Hongxiang
Hapmnioides A-C, Rearranged Labdane-Type Diterpenoids from the Chinese Liverwort Haplomitrium mnioides.
Organic letters, 2016, 18, 4274-4276
1555660 CIFC20 H20 O6P 21 21 2110.2949; 10.4128; 16.2831
90; 90; 90		1745.53Zhou, Jinchuan; Zhang, Jiaozhen; Li, Ruijuan; Liu, Jun; Fan, Peihong; Li, Yi; Ji, Mei; Dong, Yiwen; Yuan, Huiqing; Lou, Hongxiang
Hapmnioides A-C, Rearranged Labdane-Type Diterpenoids from the Chinese Liverwort Haplomitrium mnioides.
Organic letters, 2016, 18, 4274-4276
1555661 CIFC31 H26 OP -111.2411; 11.9761; 19.9127
100.2; 94.644; 113.781		2379.6Han, Ya-Ping; Song, Xian-Rong; Qiu, Yi-Feng; Li, Xue-Song; Zhang, Heng-Rui; Zhu, Xin-Yu; Liu, Xue-Yuan; Liang, Yong-Min
Lewis Acid Catalyzed Cyclization of Propargylic Alcohols with 2-Vinylphenol.
Organic letters, 2016, 18, 3866-3869
1555662 CIFC19 H13 Cl N2P -14.0802; 11.717; 15.719
92.244; 94.916; 98.11		740.2Mou, Xue-Qing; Xu, Zheng-Liang; Xu, Li; Wang, Shao-Hua; Zhang, Bang-Hong; Zhang, Di; Wang, Jie; Liu, Wei-Ting; Bao, Wen
The Synthesis of Multisubstituted Pyrroles via a Copper-Catalyzed Tandem Three-Component Reaction.
Organic letters, 2016, 18, 4032-4035
1555663 CIFC35 H40 Cl2 N4 P2 RuP -19.834; 10.604; 16.861
85.889; 78.666; 81.528		1703.5Ogata, Osamu; Nakayama, Yuji; Nara, Hideki; Fujiwhara, Mitsuhiko; Kayaki, Yoshihito
Atmospheric Hydrogenation of Esters Catalyzed by PNP-Ruthenium Complexes with an N-Heterocyclic Carbene Ligand.
Organic letters, 2016, 18, 3894-3897
1555664 CIFC100 H72.78 Br8 Cl10.5 O15.5P -119.082; 19.769; 29.22
90.481; 100.258; 92.601		10834Hillyer, Matthew B.; Gibb, Corinne L. D.; Sokkalingam, Punidha; Jordan, Jacobs H.; Ioup, Sarah E.; Mague, Joel T.; Gibb, Bruce C.
Synthesis of Water-Soluble Deep-Cavity Cavitands.
Organic letters, 2016, 18, 4048-4051
1555665 CIFC30 H46 O3P 21 21 216.3412; 17.9097; 23.6648
90; 90; 90		2687.59Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555666 CIFC45 H68 O6P 21 21 219.6502; 13.9527; 31.7405
90; 90; 90		4273.7Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555667 CIFC30 H46 O3P 1 21 111.1615; 15.7291; 16.8829
90; 105.689; 90		2853.54Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555668 CIFC30 H46 O3P 21 21 219.9104; 10.8418; 26.6369
90; 90; 90		2862.04Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555669 CIFC30 H46 O3P 21 21 2111.9618; 20.1271; 23.2612
90; 90; 90		5600.28Zhang, Ya-Long; Chen, Chen; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Zhang, Can; Sun, Hong-Bin; Luo, Jian-Guang; Kong, Ling-Yi
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Organic letters, 2016, 18, 4068-4071
1555670 CIFC57 H77 Cl3 O22P 1 21 120.6774; 5.6019; 25.4783
90; 90.3838; 90		2951.15Ma, Xiang; Bolte, Benoit; Banwell, Martin G.; Willis, Anthony C.
Total Syntheses of the Resorcylic Acid Lactones Paecilomycin F and Cochliomycin C Using an Intramolecular Loh-Type α-Allylation Reaction for Macrolide Formation.
Organic letters, 2016, 18, 4226-4229
1555671 CIFC31 H34 O2 Si2P 1 21/c 116.1117; 9.544; 19.5581
90; 111.371; 90		2800.66Rivera-Hernández, Alejandro; Fallon, Brendan J.; Ventre, Sandrine; Simon, Cédric; Tremblay, Marie-Hélène; Gontard, Geoffrey; Derat, Etienne; Amatore, Muriel; Aubert, Corinne; Petit, Marc
Regio- and Stereoselective Hydrosilylation of Unsymmetrical Alkynes Catalyzed by a Well-Defined, Low-Valent Cobalt Catalyst.
Organic letters, 2016, 18, 4242-4245
1555672 CIFC34 H34 O Si2P -19.1784; 9.8895; 17.0426
95.596; 105.569; 90.183		1482.39Rivera-Hernández, Alejandro; Fallon, Brendan J.; Ventre, Sandrine; Simon, Cédric; Tremblay, Marie-Hélène; Gontard, Geoffrey; Derat, Etienne; Amatore, Muriel; Aubert, Corinne; Petit, Marc
Regio- and Stereoselective Hydrosilylation of Unsymmetrical Alkynes Catalyzed by a Well-Defined, Low-Valent Cobalt Catalyst.
Organic letters, 2016, 18, 4242-4245
1555673 CIFC34 H30 SiP 1 21/c 114.788; 10.1322; 18.5936
90; 106.521; 90		2670.95Rivera-Hernández, Alejandro; Fallon, Brendan J.; Ventre, Sandrine; Simon, Cédric; Tremblay, Marie-Hélène; Gontard, Geoffrey; Derat, Etienne; Amatore, Muriel; Aubert, Corinne; Petit, Marc
Regio- and Stereoselective Hydrosilylation of Unsymmetrical Alkynes Catalyzed by a Well-Defined, Low-Valent Cobalt Catalyst.
Organic letters, 2016, 18, 4242-4245
1555674 CIFC17 H24 B Br O3P 1 21 110.203; 12.287; 14.177
90; 90.025; 90		1777.3Xie, Jian-Bo; Lin, Siqi; Qiao, Shuo; Li, Guigen
Asymmetric Catalytic Enantio- and Diastereoselective Boron Conjugate Addition Reactions of α-Functionalized α,β-Unsaturated Carbonyl Substrates.
Organic letters, 2016, 18, 3926-3929
1555675 CIFC15 H17 F4 N3P 1 21/n 19.1643; 8.51; 18.787
90; 97.46; 90		1452.8Shmatova, Olga I.; Khrustalev, Victor N.; Nenajdenko, Valentine G.
From Cyclic CF3-ketimines to a Family of Trifluoromethylated Nazlinine and Trypargine Analogues.
Organic letters, 2016, 18, 4494-4497
1555676 CIFC23 H25 NP -17.1533; 10.925; 12.115
75.115; 77.43; 81.256		888.4Morrison, Alec E.; Hrudka, Jeremy J.; Dudley, Gregory B.
Thermal Cycloisomerization of Putative Allenylpyridines for the Synthesis of Isoquinoline Derivatives.
Organic letters, 2016, 18, 4104-4107
1555677 CIFC14 H14 N2 O4P 21 21 216.7657; 12.1602; 16.0507
90; 90; 90		1320.53Mondal, Mukulesh; Wheeler, Kraig A.; Kerrigan, Nessan J.
Alkaloid-Catalyzed Enantioselective [3 + 2] Cycloaddition of Ketenes and Azomethine Imines.
Organic letters, 2016, 18, 4108-4111
1555678 CIFC14 H16 N2 O3P 21 21 216.7037; 8.7886; 21.923
90; 90; 90		1291.62Mondal, Mukulesh; Wheeler, Kraig A.; Kerrigan, Nessan J.
Alkaloid-Catalyzed Enantioselective [3 + 2] Cycloaddition of Ketenes and Azomethine Imines.
Organic letters, 2016, 18, 4108-4111
1555679 CIFC24 H19 Cl O3 SP -15.9791; 10.7506; 17.3037
73.509; 81.064; 73.991		1021.56Miao, Maozhong; Luo, Yi; Xu, Huaping; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun
Solvent-Controlled, Tunable Hydrosulfonylation of 3-Cyclopropylideneprop-2-en-1-ones.
Organic letters, 2016, 18, 4292-4295
1555680 CIFC24 H20 O3 SP 1 21/n 116.1137; 6.3712; 38.874
90; 92.022; 90		3988.5Miao, Maozhong; Luo, Yi; Xu, Huaping; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun
Solvent-Controlled, Tunable Hydrosulfonylation of 3-Cyclopropylideneprop-2-en-1-ones.
Organic letters, 2016, 18, 4292-4295
1555681 CIFC27.5 H23.5 Br Cl1.5 N2 O8P 19.4486; 11.0765; 16.057
73.497; 87.912; 72.63		1535.63Bender, Trandon A.; Dabrowski, Jennifer A.; Zhong, Hongyu; Gagné, Michel R
Diastereoselective B(C6F5)3-Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates.
Organic letters, 2016, 18, 4120-4123
1555682 CIFC13 H17 Br O3P 1 21 15.804; 7.1933; 15.2241
90; 94.904; 90		633.28Bender, Trandon A.; Dabrowski, Jennifer A.; Zhong, Hongyu; Gagné, Michel R
Diastereoselective B(C6F5)3-Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates.
Organic letters, 2016, 18, 4120-4123
1555683 CIFC35 H40 O10C 1 2/c 127.853; 15.8192; 16.3354
90; 93.008; 90		7187.7Dyadyuk, Alina; Sudheendran, Kavitha; Vainer, Yulia; Vershinin, Vlada; Shames, Alexander I.; Pappo, Doron
Direct Synthesis of Polyaryls by Consecutive Oxidative Cross-Coupling of Phenols with Arenes.
Organic letters, 2016, 18, 4324-4327
1555684 CIFC32 H28 F6 N4 S2R -3 :H41.1943; 41.1943; 4.9303
90; 90; 120		7245.7Ie, Yutaka; Uchida, Ayana; Kawaguchi, Nana; Nitani, Masashi; Tada, Hirokazu; Kakiuchi, Fumitoshi; Aso, Yoshio
Electron-Accepting π-Conjugated Molecules with Fluorine-Containing Dicyanovinylidene as Terminal Groups: Synthesis, Properties, and Semiconducting Characteristics.
Organic letters, 2016, 18, 4320-4323
1555685 CIFC45 H28 F18 N4 S2P 1 21/n 19.3041; 17.8786; 26.0132
90; 94.968; 90		4310.9Ie, Yutaka; Uchida, Ayana; Kawaguchi, Nana; Nitani, Masashi; Tada, Hirokazu; Kakiuchi, Fumitoshi; Aso, Yoshio
Electron-Accepting π-Conjugated Molecules with Fluorine-Containing Dicyanovinylidene as Terminal Groups: Synthesis, Properties, and Semiconducting Characteristics.
Organic letters, 2016, 18, 4320-4323
1555686 CIFC39 H28 F6 N4 S2P -111.286; 12.0729; 13.6655
86.182; 69.301; 85.413		1734.75Ie, Yutaka; Uchida, Ayana; Kawaguchi, Nana; Nitani, Masashi; Tada, Hirokazu; Kakiuchi, Fumitoshi; Aso, Yoshio
Electron-Accepting π-Conjugated Molecules with Fluorine-Containing Dicyanovinylidene as Terminal Groups: Synthesis, Properties, and Semiconducting Characteristics.
Organic letters, 2016, 18, 4320-4323
1555687 CIFC16 H23 N O2P 21 21 217.4804; 10.4902; 18.4048
90; 90; 90		1444.24Ma, Donghui; Zhong, Zhuliang; Liu, Zaimin; Zhang, Mingjie; Xu, Shiyan; Xu, Dengyu; Song, Dengpeng; Xie, Xingang; She, Xuegong
Protecting-Group-Free Total Synthesis of (-)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization.
Organic letters, 2016, 18, 4328-4331
1555688 CIFC16 H23 N O2P 21 21 2110.9468; 13.1316; 19.8805
90; 90; 90		2857.8Ma, Donghui; Zhong, Zhuliang; Liu, Zaimin; Zhang, Mingjie; Xu, Shiyan; Xu, Dengyu; Song, Dengpeng; Xie, Xingang; She, Xuegong
Protecting-Group-Free Total Synthesis of (-)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization.
Organic letters, 2016, 18, 4328-4331
1555689 CIFC13 H19 N O2P 1 21 17.6484; 7.0465; 10.9071
90; 98.254; 90		581.74Ma, Donghui; Zhong, Zhuliang; Liu, Zaimin; Zhang, Mingjie; Xu, Shiyan; Xu, Dengyu; Song, Dengpeng; Xie, Xingang; She, Xuegong
Protecting-Group-Free Total Synthesis of (-)-Lycopodine via Phosphoric Acid Promoted Alkyne Aza-Prins Cyclization.
Organic letters, 2016, 18, 4328-4331
1555690 CIFC27 H24 F N O2P n a 219.672; 25.53; 9.182
90; 90; 90		2267.3Rajesh, Manda; Puri, Surendra; Kant, Ruchir; Sridhar Reddy, Maddi
Synthesis of Substituted Furan/Pyrrole-3-carboxamides through a Tandem Nucleopalladation and Isocyanate Insertion.
Organic letters, 2016, 18, 4332-4335
1555691 CIFC9 H16 B Br2 P SP b c a7.1372; 12.6521; 31.0391
90; 90; 90		2802.8Imamoto, Tsuneo; Horiuchi, Yumi; Tamura, Ken; Sugiya, Masashi; Masu, Hyuma
Catalyst-Free and Regioconvergent Substitution Reactions of Bromothiophenes with a BH3-Substituted Phosphide Anion.
Organic letters, 2016, 18, 4132-4135
1555692 CIFC9 H16 B Br2 P SP 1 21/n 110.1556; 12.2943; 11.2898
90; 101.946; 90		1379.07Imamoto, Tsuneo; Horiuchi, Yumi; Tamura, Ken; Sugiya, Masashi; Masu, Hyuma
Catalyst-Free and Regioconvergent Substitution Reactions of Bromothiophenes with a BH3-Substituted Phosphide Anion.
Organic letters, 2016, 18, 4132-4135
1555693 CIFC36 H36 N2 O3P 1 21 111.3376; 9.2055; 14.8038
90; 106.365; 90		1482.45Zhang, Jia-Xing; Wang, Hong-Yu; Jin, Qiao-Wen; Zheng, Chang-Wu; Zhao, Gang; Shang, Yong-Jia
Thiourea-Quaternary Ammonium Salt Catalyzed Asymmetric 1, 3-Dipolar Cycloaddition of Imino Esters To Construct Spiro[pyrrolidin-3,3'-oxindoles].
Organic letters, 2016, 18, 4774-4777
1555694 CIFC16 H13 N O2C 1 2 132.3; 4.861; 20.038
90; 126.539; 90		2528Feng, Minghao; Tang, Bingqing; Xu, Hong-Xi; Jiang, Xuefeng
Collective Synthesis of Phenanthridinone through C-H Activation Involving a Pd-Catalyzed Aryne Multicomponent Reaction.
Organic letters, 2016, 18, 4352-4355
1555695 CIFC19 H19 Cl O3P 21 21 218.4147; 9.8374; 20.9238
90; 90; 90		1732Su, Yan; Li, Qing-Fang; Zhao, Yu-Ming; Gu, Peiming
Preparation of Optically Active cis-Cyclopropane Carboxylates: Cyclopropanation of α-Silyl Stryenes with Aryldiazoacetates and Desilylation of the Resulting Silyl Cyclopropanes.
Organic letters, 2016, 18, 4356-4359
1555696 CIFC21 H25 Br O2 SiP 21 21 218.9734; 9.5887; 24.3831
90; 90; 90		2098Su, Yan; Li, Qing-Fang; Zhao, Yu-Ming; Gu, Peiming
Preparation of Optically Active cis-Cyclopropane Carboxylates: Cyclopropanation of α-Silyl Stryenes with Aryldiazoacetates and Desilylation of the Resulting Silyl Cyclopropanes.
Organic letters, 2016, 18, 4356-4359
1555697 CIFC17 H14 O5P -18.115; 9.202; 10.049
99.389; 94.177; 102.638		717.8Xiang, Jia-Chen; Cheng, Yan; Wang, Miao; Wu, Yan-Dong; Wu, An-Xin
Direct Construction of 4-Hydroxybenzils via Para-Selective C-C Bond Coupling of Phenols and Aryl Methyl Ketones.
Organic letters, 2016, 18, 4360-4363
1555698 CIFC15 H12 O3C 1 2/c 113.771; 8.568; 20.892
90; 100.249; 90		2425.7Xiang, Jia-Chen; Cheng, Yan; Wang, Miao; Wu, Yan-Dong; Wu, An-Xin
Direct Construction of 4-Hydroxybenzils via Para-Selective C-C Bond Coupling of Phenols and Aryl Methyl Ketones.
Organic letters, 2016, 18, 4360-4363
1555699 CIFC20 H16 O3P 1 21/n 17.9918; 8.696; 22.75
90; 98.022; 90		1565.6Xiang, Jia-Chen; Cheng, Yan; Wang, Miao; Wu, Yan-Dong; Wu, An-Xin
Direct Construction of 4-Hydroxybenzils via Para-Selective C-C Bond Coupling of Phenols and Aryl Methyl Ketones.
Organic letters, 2016, 18, 4360-4363
1555700 CIFC23 H43 N2 O10 P SP 21 21 2110.3757; 11.5557; 24.7257
90; 90; 90		2964.57Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555701 CIFC16 H30 N2 O7 SP 21 21 2110.1789; 11.9132; 18.0755
90; 90; 90		2191.89Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555702 CIFC22 H38 N2 O9 SP 21 21 2110.2553; 11.3826; 23.6017
90; 90; 90		2755.07Lin, Long-Zhi; Fang, Jim-Min
Total Synthesis of Anti-Influenza Agents Zanamivir and Zanaphosphor via Asymmetric Aza-Henry Reaction.
Organic letters, 2016, 18, 4400-4403
1555703 CIFC16 H21 N O2P 21 21 218.5903; 9.1195; 17.5588
90; 90; 90		1375.54Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555704 CIFC16 H21 N O2P 21 21 218.7114; 9.1691; 16.9047
90; 90; 90		1350.27Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555705 CIFC16 H19 N O4P 21 21 217.8847; 12.731; 13.5189
90; 90; 90		1357.03Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555706 CIFC16 H21 N O2P 21 21 218.7313; 10.0431; 14.6801
90; 90; 90		1287.29Tang, Yu; Xiong, Juan; Zhang, Jing-Jing; Wang, Wei; Zhang, Hai-Yan; Hu, Jin-Feng
Annotinolides A-C, Three Lycopodane-Derived 8,5-Lactones with Polycyclic Skeletons from Lycopodium annotinum.
Organic letters, 2016, 18, 4376-4379
1555707 CIFC26 H22 SiP 1 21 111.087; 7.621; 12.555
90; 112.697; 90		978.7Murai, Masahito; Okada, Ryo; Nishiyama, Atsushi; Takai, Kazuhiko
Synthesis and Properties of Sila[n]helicenes via Dehydrogenative Silylation of C-H Bonds under Rhodium Catalysis.
Organic letters, 2016, 18, 4380-4383
1555708 CIFC18 H21 N3P n a 2114.58554; 8.33918; 25.4351
90; 90; 90		3093.71Kim, Seyong; Jo, Junyong; Lee, Dongwhan
Conformationally Distorted π-Conjugation for Reaction-Based Detection of Nickel: Fluorescence Turn-on by Twist-and-Fragment.
Organic letters, 2016, 18, 4530-4533
1555709 CIFC58 H47 Cl2 F6 P3 Pd3C 1 2/c 145.749; 10.2559; 26.996
90; 122.902; 90		10634.8Deng, Xiao-Yun; Lin, Jin-Hong; Xiao, Ji-Chang
Pd-Catalyzed Transfer of Difluorocarbene.
Organic letters, 2016, 18, 4384-4387
1555710 CIFC14 H8 F N O2P 1 21/n 112.021; 3.7932; 23.197
90; 90.203; 90		1057.7Verma, Ajay; Kumar, Sangit
Selective Oxidative Decarbonylative Cleavage of Unstrained C(sp(3))-C(sp(2)) Bond: Synthesis of Substituted Benzoxazinones.
Organic letters, 2016, 18, 4388-4391
1555711 CIFC14 H7 Br N2 O4P 21 21 213.8804; 7.5188; 43.727
90; 90; 90		1275.8Verma, Ajay; Kumar, Sangit
Selective Oxidative Decarbonylative Cleavage of Unstrained C(sp(3))-C(sp(2)) Bond: Synthesis of Substituted Benzoxazinones.
Organic letters, 2016, 18, 4388-4391
1555712 CIFC91 H86 Cl6 N6 O7P -114.8278; 15.0838; 20.0662
108.103; 97.486; 103.078		4056.5Yeon, Yerim; Leem, Soojung; Wagen, Corin; Lynch, Vincent M.; Kim, Sung Kuk; Sessler, Jonathan L.
3-(Dicyanomethylidene)indan-1-one-Functionalized Calix[4]arene-Calix[4]pyrrole Hybrid: An Ion-Pair Sensor for Cesium Salts.
Organic letters, 2016, 18, 4396-4399
1555713 CIFC108 H103 N9 O6 SP 1 21/c 120.026; 36.681; 14.516
90; 110.35; 90		9998Jeon, Hae-Geun; Jang, Han Bit; Kang, Philjae; Choi, Ye Rin; Kim, Junyoung; Lee, Ji Hyun; Choi, Moon-Gun; Jeong, Kyu-Sung
Helical Aromatic Foldamers Functioning as a Fluorescence Turn-on Probe for Anions.
Organic letters, 2016, 18, 4404-4407
1555714 CIFC112 H114 N8 O8P b c a16.057; 36.163; 40.408
90; 90; 90		23464Jeon, Hae-Geun; Jang, Han Bit; Kang, Philjae; Choi, Ye Rin; Kim, Junyoung; Lee, Ji Hyun; Choi, Moon-Gun; Jeong, Kyu-Sung
Helical Aromatic Foldamers Functioning as a Fluorescence Turn-on Probe for Anions.
Organic letters, 2016, 18, 4404-4407
1555715 CIFC13 H24 O4P 1 21 18.9435; 8.7011; 9.261
90; 99.32; 90		711.162Cornil, Johan; Echeverria, Pierre-Georges; Reymond, Sébastien; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie; Guérinot, Amandine; Cossy, Janine
Synthetic Studies toward the C14-C29 Fragment of Mirabalin.
Organic letters, 2016, 18, 4534-4537
1555716 CIFC19 H12 Br2 N4P 1 21/c 111.851; 12.377; 11.931
90; 108.65; 90		1658.1Ghorbani, Mahdi; Mohammadi, Bagher; Saraii, Mahnaz; Masoumi, Bakhshali; Abbasian, Mojtaba; Ramazani, Ali; Slepokura, Katarzyna; Lis, Tadeusz
A Three-Component Reaction for the Synthesis of 1-Azabicyclo[3.1.0]hexane-3-enes.
Organic letters, 2016, 18, 4759-4761
1555717 CIFC24 H35 Br N2 O2 SiP -111.7811; 12.1808; 17.8426
80.372; 88.311; 87.675		2521.7Jing, Changcheng; Cheng, Qing-Qing; Deng, Yongming; Arman, Hadi; Doyle, Michael P.
Highly Regio- and Enantioselective Formal [3 + 2]-Annulation of Indoles with Electrophilic Enol Carbene Intermediates.
Organic letters, 2016, 18, 4550-4553
1555718 CIFC27 H35 N O SiP 1 21/c 18.5706; 31.946; 9.0911
90; 99.794; 90		2452.8Malone, Joshua A.; Cleveland, Alexander H.; Fronczek, Frank R.; Kartika, Rendy
Effects of Solvent and Residual Water on Enhancing the Reactivity of Six-Membered Silyloxyallyl Cations toward Nucleophilic Addition.
Organic letters, 2016, 18, 4408-4411
1555719 CIFC21 H30 Br N O SiP 1 21/n 112.2375; 14.2198; 13.0699
90; 113.855; 90		2080.06Malone, Joshua A.; Cleveland, Alexander H.; Fronczek, Frank R.; Kartika, Rendy
Effects of Solvent and Residual Water on Enhancing the Reactivity of Six-Membered Silyloxyallyl Cations toward Nucleophilic Addition.
Organic letters, 2016, 18, 4408-4411
1555720 CIFC29.64 H34.56 O10.36P 21 21 216.9086; 13.0711; 29.2663
90; 90; 90		2642.8Zhou, Ming; Liu, Ye; Song, Jian; Peng, Xiao-Gang; Cheng, Qi; Cao, Hui; Xiang, Ming; Ruan, Han-Li
Schincalide A, a Schinortriterpenoid with a Tricyclo[5.2.1.0(1,6)]decane-Bridged System from the Stems and Leaves of Schisandra incarnate.
Organic letters, 2016, 18, 4558-4561
1555721 CIFC24 H19 N3 OP -19.973; 10.372; 19.048
104.203; 90.641; 96.358		1896.8Wang, Weiguo; Wei, Fang; Ma, Yudao; Tung, Chen-Ho; Xu, Zhenghu
Copper(I)-Catalyzed Three-Component Click/Alkynylation: One-Pot Synthesis of 5-Alkynyl-1,2,3-triazoles.
Organic letters, 2016, 18, 4158-4161
1555722 CIFC9 H9 N3 OP 1 21/c 117.673; 5.8274; 8.4242
90; 92.611; 90		866.7Taylor, Scott D.; Lohani, Chuda Raj
A Fresh Look at the Staudinger Reaction on Azido Esters: Formation of 2H-1,2,3-Triazol-4-ols from α-Azido Esters Using Trialkyl Phosphines.
Organic letters, 2016, 18, 4412-4415
1555723 CIFC69 H33 N9 O6P 1 21/n 114.669; 32.397; 19.484
90; 111.648; 90		8606Wang, Zhen; Luo, Yi; Zhai, Tian-Long; Ma, Hui; Chen, Jing-Jing; Shu, Yuanjie; Zhang, Chun
Porous Triphenylbenzene-Based Bicyclooxacalixarene Cage for Selective Adsorption of CO2/N2.
Organic letters, 2016, 18, 4574-4577
1555724 CIFC29 H22 N O2P 1 21/c 113.386; 22.1035; 15.0948
90; 90.213; 90		4466.2Cai, Zhong-Jian; Li, Fang-Hui; Wang, Shun-Yi; Ji, Shun-Jun
Palladium-Catalyzed Cascade Arene/Alkyne Annulation: Synthesis of Fluorene-Benzoxazine Derivatives.
Organic letters, 2016, 18, 4810-4813
1555725 CIFC27 H16 F N OP 21 21 217.3458; 11.9086; 21.862
90; 90; 90		1912.45Cai, Zhong-Jian; Li, Fang-Hui; Wang, Shun-Yi; Ji, Shun-Jun
Palladium-Catalyzed Cascade Arene/Alkyne Annulation: Synthesis of Fluorene-Benzoxazine Derivatives.
Organic letters, 2016, 18, 4810-4813
1555726 CIFC16 H19 N O4P b c a12.7082; 10.0795; 24.4296
90; 90; 90		3129.2Bantreil, Xavier; Bourderioux, Aurélie; Mateo, Pierre; Hagerman, Caroline E.; Selkti, Mohamed; Brachet, Etienne; Belmont, Philippe
Phosphine-Triggered Selectivity Switch in Silver-Catalyzed o-Alkynylbenzohydroxamic Acid Cycloisomerizations.
Organic letters, 2016, 18, 4814-4817
1555727 CIFC18 H21 N3 O7 SP 1 21 110.5129; 8.026; 12.3315
90; 99.836; 90		1025.19Glibstrup, Emil; Pedersen, Christian Marcus
Scalable Synthesis of Anomerically Pure Orthogonal-Protected GlcN3 and GalN3 from d-Glucosamine.
Organic letters, 2016, 18, 4424-4427
1555728 CIFC20 H19 N3 O2P -18.9053; 9.1342; 10.3857
85.819; 88.672; 77.281		821.86Li, Zexian; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Palladium-Catalyzed Regioselective C8-H Amination of 1-Naphthylamine Derivatives with Aliphatic Amines.
Organic letters, 2016, 18, 4594-4597
1555729 CIFC17 H25 N O4P 1 21 111.69; 5.133; 14.52
90; 109.05; 90		824Morita, Tomohiro; Akita, Mitsutoshi; Satoh, Tetsuya; Kakiuchi, Fumitoshi; Miura, Masahiro
Ruthenium-Catalyzed Cross-Coupling of Maleimides with Alkenes.
Organic letters, 2016, 18, 4598-4601
1555730 CIFC12 H14 N2 OC 1 c 18.1402; 15.085; 8.9672
90; 104.569; 90		1065.7Luo, Bo; Gao, Jin-Ming; Lautens, Mark
Palladium-Catalyzed Norbornene-Mediated Tandem Amination/Cyanation Reaction: A Method for the Synthesis of ortho-Aminated Benzonitriles.
Organic letters, 2016, 18, 4166-4169
1555731 CIFC16 H21 N3 O2P -19.1894; 9.4311; 10.3177
105.277; 93.849; 116.71		752.5Luo, Bo; Gao, Jin-Ming; Lautens, Mark
Palladium-Catalyzed Norbornene-Mediated Tandem Amination/Cyanation Reaction: A Method for the Synthesis of ortho-Aminated Benzonitriles.
Organic letters, 2016, 18, 4166-4169
1555732 CIFC33 H38 N2 O8 S2P -18.8389; 10.1118; 20.365
91.087; 95.709; 107.236		1727.56Wang, Bin; Liang, Man; Tang, Jian; Deng, Yuting; Zhao, Jinhong; Sun, Hao; Tung, Chen-Ho; Jia, Jiong; Xu, Zhenghu
Gold/Lewis Acid Catalyzed Cycloisomerization/Diastereoselective [3 + 2] Cycloaddition Cascade: Synthesis of Diverse Nitrogen-Containing Spiro Heterocycles.
Organic letters, 2016, 18, 4614-4617
1555733 CIFC33 H37 Br N2 O8 S2P -18.76; 10.03; 20.67
97.61; 97.04; 107.15		1695Wang, Bin; Liang, Man; Tang, Jian; Deng, Yuting; Zhao, Jinhong; Sun, Hao; Tung, Chen-Ho; Jia, Jiong; Xu, Zhenghu
Gold/Lewis Acid Catalyzed Cycloisomerization/Diastereoselective [3 + 2] Cycloaddition Cascade: Synthesis of Diverse Nitrogen-Containing Spiro Heterocycles.
Organic letters, 2016, 18, 4614-4617
1555734 CIFC30 H31 N O7 SP -19.901; 11.342; 13.766
97.9523; 97.714; 115.282		1351.7Wang, Bin; Liang, Man; Tang, Jian; Deng, Yuting; Zhao, Jinhong; Sun, Hao; Tung, Chen-Ho; Jia, Jiong; Xu, Zhenghu
Gold/Lewis Acid Catalyzed Cycloisomerization/Diastereoselective [3 + 2] Cycloaddition Cascade: Synthesis of Diverse Nitrogen-Containing Spiro Heterocycles.
Organic letters, 2016, 18, 4614-4617
1555735 CIFC30 H31 N O7 SP -18.22; 13.26; 13.66
62.43; 75.81; 86.19		1278Wang, Bin; Liang, Man; Tang, Jian; Deng, Yuting; Zhao, Jinhong; Sun, Hao; Tung, Chen-Ho; Jia, Jiong; Xu, Zhenghu
Gold/Lewis Acid Catalyzed Cycloisomerization/Diastereoselective [3 + 2] Cycloaddition Cascade: Synthesis of Diverse Nitrogen-Containing Spiro Heterocycles.
Organic letters, 2016, 18, 4614-4617
1555736 CIFC51 H18 F51 I3 N6 O3P -111.539; 16.419; 18.984
77.096; 85.285; 73.926		3368Sun, Xiaoyang; Wang, Wenmin; Li, Yanle; Ma, Jing; Yu, Shouyun
Halogen-Bond-Promoted Double Radical Isocyanide Insertion under Visible-Light Irradiation: Synthesis of 2-Fluoroalkylated Quinoxalines.
Organic letters, 2016, 18, 4638-4641
1555737 CIFC17 H6 F17 I N2 OP -15.3794; 8.0586; 26.339
81.743; 86.002; 76.923		1099.8Sun, Xiaoyang; Wang, Wenmin; Li, Yanle; Ma, Jing; Yu, Shouyun
Halogen-Bond-Promoted Double Radical Isocyanide Insertion under Visible-Light Irradiation: Synthesis of 2-Fluoroalkylated Quinoxalines.
Organic letters, 2016, 18, 4638-4641
1555738 CIFC16 H13 N O2 SP 1 21/c 19.6089; 9.7376; 14.4701
90; 96.693; 90		1344.71Du, Bingnan; Qian, Ping; Wang, Yang; Mei, Haibo; Han, Jianlin; Pan, Yi
Cu-Catalyzed Deoxygenative C2-Sulfonylation Reaction of Quinoline N-Oxides with Sodium Sulfinate.
Organic letters, 2016, 18, 4144-4147
1555739 CIFC21 H23 B O3P 1 21/n 18.3423; 14.044; 15.465
90; 92.323; 90		1810.4Jakhar, Vineet Kumar; Barman, Milan Kr; Nembenna, Sharanappa
Aluminum Monohydride Catalyzed Selective Hydroboration of Carbonyl Compounds.
Organic letters, 2016, 18, 4710-4713
1555740 CIFC27 H44 Al N3P 1 21/c 112.2925; 12.5244; 16.9143
90; 98.731; 90		2573.9Jakhar, Vineet Kumar; Barman, Milan Kr; Nembenna, Sharanappa
Aluminum Monohydride Catalyzed Selective Hydroboration of Carbonyl Compounds.
Organic letters, 2016, 18, 4710-4713
1555741 CIFC15 H23 N O3P 21 21 218.5731; 9.2969; 17.1079
90; 90; 90		1363.56Xu, Shiyan; Zhang, Jing; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Asymmetric Total Synthesis of (-)-Lycospidine A.
Organic letters, 2016, 18, 4682-4685
1555742 CIFC15 H19 Cl2 N O2P 6114.6129; 14.6129; 14.5834
90; 90; 120		2696.88Xu, Shiyan; Zhang, Jing; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Asymmetric Total Synthesis of (-)-Lycospidine A.
Organic letters, 2016, 18, 4682-4685
1555743 CIFC15 H21 N O3P 43 21 28.4853; 8.4853; 37.19
90; 90; 90		2677.69Xu, Shiyan; Zhang, Jing; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Asymmetric Total Synthesis of (-)-Lycospidine A.
Organic letters, 2016, 18, 4682-4685
1555744 CIFC52 H56 N2 Si2P -17.8003; 16.2905; 17.4071
79.797; 87.838; 87.209		2173.4Antonicelli, Gabriella; Gozalvez, Cristian; Atxabal, Ainhoa; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio
K-Conjugated Dibenzoazahexacenes.
Organic letters, 2016, 18, 4694-4697
1555745 CIFC50 H54 N4 Si2P -17.7643; 16.145; 17.4579
80.174; 88.112; 87.207		2153.1Antonicelli, Gabriella; Gozalvez, Cristian; Atxabal, Ainhoa; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio
K-Conjugated Dibenzoazahexacenes.
Organic letters, 2016, 18, 4694-4697
1555746 CIFC43 H52 Cl6 N2 O8C 2 2 2118.3635; 25.2508; 9.9745
90; 90; 90		4625.1Garcia, Alfredo; Drown, Bryon S.; Hergenrother, Paul J.
Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.
Organic letters, 2016, 18, 4852-4855
1555747 CIFC19 H21 N O4P 21 21 218.4444; 10.0554; 18.0941
90; 90; 90		1536.4Garcia, Alfredo; Drown, Bryon S.; Hergenrother, Paul J.
Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.
Organic letters, 2016, 18, 4852-4855
1555748 CIFC27.5 H26 Br3 Cl N2 OP -110.1204; 17.4091; 19.0464
90.665; 104.582; 94.448		3236.2Janssen-Müller, Daniel; Singha, Santanu; Olyschläger, Theresa; Daniliuc, Constantin G.; Glorius, Frank
Annulation of o-Quinodimethanes through N-Heterocyclic Carbene Catalysis for the Synthesis of 1-Isochromanones.
Organic letters, 2016, 18, 4444-4447
1555749 CIFC12 H9 F3 O4P 1 21/c 113.301; 5.8835; 15.051
90; 98.531; 90		1164.8Janssen-Müller, Daniel; Singha, Santanu; Olyschläger, Theresa; Daniliuc, Constantin G.; Glorius, Frank
Annulation of o-Quinodimethanes through N-Heterocyclic Carbene Catalysis for the Synthesis of 1-Isochromanones.
Organic letters, 2016, 18, 4444-4447
1555750 CIFC30 H49 Li Ni O8P -18.67174; 12.0843; 15.4857
86.329; 78.921; 74.044		1531.07Iwasaki, Takanori; Fukuoka, Asuka; Min, Xin; Yokoyama, Wataru; Kuniyasu, Hitoshi; Kambe, Nobuaki
Multicomponent Coupling Reaction of Perfluoroarenes with 1,3-Butadiene and Aryl Grignard Reagents Promoted by an Anionic Ni(II) Complex.
Organic letters, 2016, 18, 4868-4871
1555751 CIFC23 H29 Cl3 N2 O3 SP 21 21 2110.8104; 11.1726; 21.1349
90; 90; 90		2552.68Zhang, Juan; Chen, Zhi-Xiong; Du, Ting; Li, Bing; Gu, Yonghong; Tian, Shi-Kai
Aryne-Mediated [2,3]-Sigmatropic Rearrangement of Tertiary Allylic Amines.
Organic letters, 2016, 18, 4872-4875
1555752 CIFC22 H26 Br N3 O3 SP 1 21 19.1897; 10.1219; 12.6525
90; 95.598; 90		1171.29Zhang, Juan; Chen, Zhi-Xiong; Du, Ting; Li, Bing; Gu, Yonghong; Tian, Shi-Kai
Aryne-Mediated [2,3]-Sigmatropic Rearrangement of Tertiary Allylic Amines.
Organic letters, 2016, 18, 4872-4875
1555753 CIFC18 H17 Cl N2 O2 SP 1 21/c 111.48668; 7.37203; 20.25344
90; 106.033; 90		1648.35Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Functionalization of Alkenes through Telescoped Continuous Flow Aziridination Processes.
Organic letters, 2016, 18, 4908-4911
1555754 CIFC15 H17 I N2 O3 SP 1 21/n 18.9249; 12.0771; 15.5355
90; 98.2881; 90		1657.03Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Functionalization of Alkenes through Telescoped Continuous Flow Aziridination Processes.
Organic letters, 2016, 18, 4908-4911
1555755 CIFC28 H27 N O2P -111.3527; 11.6672; 16.7434
96.567; 95.824; 102.162		2135.7Huang, Yu-Wen; Frontier, Alison J.
Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems.
Organic letters, 2016, 18, 4896-4899
1555756 CIFC24 H23 N O3P 21 21 216.9578; 11.041; 24.685
90; 90; 90		1896.3Huang, Yu-Wen; Frontier, Alison J.
Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems.
Organic letters, 2016, 18, 4896-4899
1555757 CIFC21 H22 N2 O3P -18.5529; 9.1794; 12.3004
75.507; 77.927; 82.204		910.75Foley, Christopher; Shaw, Arthur; Hulme, Christopher
Two-Step Route to Diverse N-Functionalized Peptidomimetic-like Isatins through an Oxidation/Intramolecular Oxidative-Amidation Cascade of Ugi Azide and Ugi Three-Component Reaction Products.
Organic letters, 2016, 18, 4904-4907
1555758 CIFC25 H23 N O4P 1 21/c 18.1296; 15.4679; 33.0511
90; 94.9069; 90		4140.9Chen, Cuili; Zou, Yongzhen; Chen, Xianxiao; Zhang, Xiaoxiang; Rao, Weidong; Chan, Philip Wai Hong
Gold-Catalyzed Tandem 1,3-Migration/Double Cyclopropanation of 1-Ene-4,n-diyne Esters to Tetracyclodecene and Tetracycloundecene Derivatives.
Organic letters, 2016, 18, 4730-4733
1555759 CIFC17 H18 OP 1 21/c 18.1119; 15.0586; 10.8705
90; 101.345; 90		1301.93Chen, Cuili; Zou, Yongzhen; Chen, Xianxiao; Zhang, Xiaoxiang; Rao, Weidong; Chan, Philip Wai Hong
Gold-Catalyzed Tandem 1,3-Migration/Double Cyclopropanation of 1-Ene-4,n-diyne Esters to Tetracyclodecene and Tetracycloundecene Derivatives.
Organic letters, 2016, 18, 4730-4733
1555760 CIFC25 H27 O6P 1 21/c 111.481; 13.8874; 14.2299
90; 111.405; 90		2112.3Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang
Catalytic Enantioselective Total Synthesis of Hypocrolide A.
Organic letters, 2016, 18, 4932-4935
1555761 CIFC29 H30 N2 O8P 1 21/c 128.362; 5.9866; 16.1832
90; 100.97; 90		2697.6Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang
Catalytic Enantioselective Total Synthesis of Hypocrolide A.
Organic letters, 2016, 18, 4932-4935
1555762 CIFC15 H24 O4P 1 21/c 19.22; 9.221; 17.022
90; 95.108; 90		1441.4Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang
Catalytic Enantioselective Total Synthesis of Hypocrolide A.
Organic letters, 2016, 18, 4932-4935
1555763 CIFC25 H26 O6P n a 2115.6433; 8.7737; 31.105
90; 90; 90		4269.1Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang
Catalytic Enantioselective Total Synthesis of Hypocrolide A.
Organic letters, 2016, 18, 4932-4935
1555764 CIFC17 H18 N O6C 1 2 120.9111; 10.4665; 15.9414
90; 105.059; 90		3369.21Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang
Catalytic Enantioselective Total Synthesis of Hypocrolide A.
Organic letters, 2016, 18, 4932-4935
1555765 CIFC23 H30 N2 O7P 1 21/n 19.0774; 15.15; 16.882
90; 93.62; 90		2317Yang, Changjiang; Liu, Wei; He, Zijian; He, Zhengjie
Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles.
Organic letters, 2016, 18, 4936-4939
1555766 CIFC13 H13 Br N2 O3P -18.296; 8.793; 10.13
100.061; 106.015; 108.472		645.2Yang, Changjiang; Liu, Wei; He, Zijian; He, Zhengjie
Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles.
Organic letters, 2016, 18, 4936-4939
1555767 CIFC19 H21 N O2P 21 21 215.3836; 31.775; 9.5511
90; 90; 90		1633.85Lynch, Denis; Deasy, Rebecca E.; Clarke, Leslie-Ann; Slattery, Catherine N.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Magnus, Nicholas A.; Moynihan, Humphrey A.
Exploring the Scope of Asymmetric Synthesis of β-Hydroxy-γ-lactams via Noyori-type Reductions.
Organic letters, 2016, 18, 4978-4981
1555768 CIFC19 H27 N O2P 1 21 111.0767; 6.1023; 13.1637
90; 104.848; 90		860.07Lynch, Denis; Deasy, Rebecca E.; Clarke, Leslie-Ann; Slattery, Catherine N.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Magnus, Nicholas A.; Moynihan, Humphrey A.
Exploring the Scope of Asymmetric Synthesis of β-Hydroxy-γ-lactams via Noyori-type Reductions.
Organic letters, 2016, 18, 4978-4981
1555769 CIFC25 H29 N O9 SP 1 21/c 121.365; 9.334; 26.587
90; 92.256; 90		5298Ghosh, Asit; Mandal, Subhajit; Chattaraj, Pratim Kumar; Banerjee, Prabal
Ring Expansion of Donor-Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights.
Organic letters, 2016, 18, 4940-4943
1555770 CIFC26 H31 N O6C 1 2/c 121.286; 12.49; 20.712
90; 118.061; 90		4859Ghosh, Asit; Mandal, Subhajit; Chattaraj, Pratim Kumar; Banerjee, Prabal
Ring Expansion of Donor-Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights.
Organic letters, 2016, 18, 4940-4943
1555771 CIFC49 H53 B3 F6 N6P b n m8.651; 18.3861; 29.434
90; 90; 90		4681.7Ozdemir, Tugba; Bila, Jose Luis; Sozmen, Fazli; Yildirim, Leyla T.; Akkaya, Engin U.
Orthogonal Bodipy Trimers as Photosensitizers for Photodynamic Action.
Organic letters, 2016, 18, 4821-4823
1555772 CIFC35 H33 N O6P -18.6021; 11.6111; 16.938
70.766; 89.038; 68.763		1478.7Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach.
Organic letters, 2016, 18, 5208-5211
1555773 CIFC28 H25 N O2P -19.92; 11.199; 12.122
64.365; 68.38; 81.92		1128.4Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach.
Organic letters, 2016, 18, 5208-5211
1555774 CIFC37 H41 N3 O6P -111.0788; 11.3956; 13.782
74.825; 88.857; 85.704		1674.6Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach.
Organic letters, 2016, 18, 5208-5211
1555775 CIFC9 H8 Cl N O2P 21 21 215.961; 7.819; 20.316
90; 90; 90		946.9Gao, Mingchun; Xu, Bin
Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins.
Organic letters, 2016, 18, 4746-4749
1555776 CIFC10 H8 N2 O2 SP 21 21 216.758; 8.245; 18.741
90; 90; 90		1044.2Gao, Mingchun; Xu, Bin
Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins.
Organic letters, 2016, 18, 4746-4749
1555777 CIFC14 H18 N2 O2P 1 21/c 18.018; 16.118; 10.272
90; 94.878; 90		1322.7Gao, Mingchun; Xu, Bin
Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins.
Organic letters, 2016, 18, 4746-4749
1555778 CIFC21 H18 O2P 21 21 2112.151; 23.564; 5.864
90; 90; 90		1679Li, Jingfu; Chang, Wenju; Ren, Wenlong; Dai, Jie; Shi, Yian
Palladium-Catalyzed Highly Regio- and Enantioselective Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2016, 18, 5456-5459
1555779 CIFC21 H24 Br2 O3P -110.2906; 13.6532; 15.2519
81.694; 78.662; 68.752		1951.9Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A.
Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes.
Organic letters, 2016, 18, 5018-5021
1555780 CIFC14 H21 Br OP 1 21/c 115.8482; 6.3578; 12.9413
90; 90.951; 90		1303.78Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A.
Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes.
Organic letters, 2016, 18, 5018-5021
1555781 CIFC15 H25 Br O2P n a 2110.9219; 22.3462; 13.7789
90; 90; 90		3362.9Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A.
Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes.
Organic letters, 2016, 18, 5018-5021
1555782 CIFC14 H21 Br OP 1 21/c 16.2175; 13.6079; 15.1894
90; 93.374; 90		1282.9Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A.
Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes.
Organic letters, 2016, 18, 5018-5021
1555783 CIFC15 H25 Br O2C 1 2/c 131.909; 22.347; 13.1317
90; 97.044; 90		9293.2Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A.
Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes.
Organic letters, 2016, 18, 5018-5021
1555784 CIFC31 H27 N O6 SP -110.8777; 11.0084; 13.1029
112.434; 105.665; 98.631		1338.75Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao
AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality.
Organic letters, 2016, 18, 5022-5025
1555785 CIFC31 H25 N O7 SP -110.0018; 11.5034; 12.0989
88.001; 75.075; 78.255		1316.69Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao
AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality.
Organic letters, 2016, 18, 5022-5025
1555786 CIFC32 H29 N O6 SP 1 21/n 111.089; 21.075; 12.128
90; 97.24; 90		2811.7Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao
AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality.
Organic letters, 2016, 18, 5022-5025
1555787 CIFC32 H29 N O6 SP 1 21/c 111.544; 14.011; 17.128
90; 99.02; 90		2736.1Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao
AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality.
Organic letters, 2016, 18, 5022-5025
1555788 CIFC31 H27 N O6 SP -19.6744; 11.557; 12.09
86.67; 80.45; 87.22		1329.7Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao
AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality.
Organic letters, 2016, 18, 5022-5025
1555789 CIFC74 H18 F30 N8P 1 21/n 117.864; 23.111; 18.348
90; 110.537; 90		7094Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu
Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches.
Organic letters, 2016, 18, 5046-5049
1555790 CIFC40 H18 F15 N5 OP 1 21/n 116.2619; 30.2509; 10.0784
90; 133.451; 90		3599.3Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu
Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches.
Organic letters, 2016, 18, 5046-5049
1555791 CIFC43 H19 Cl2 F15 N4 Ni O2P -112.7733; 12.9992; 14.5801
95.103; 107.136; 114.829		2035.5Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu
Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches.
Organic letters, 2016, 18, 5046-5049
1555792 CIFC30 H24 N2 O4 S2P 1 21/c 110.4528; 14.3902; 8.7251
90; 92.7628; 90		1310.89Seo, Boram; Kim, Ya Gob; Lee, Phil Ho
Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles.
Organic letters, 2016, 18, 5050-5053
1555793 CIFC30 H22 Br2 N2 O4 S2P 17.9207; 9.0758; 11.1924
80.79; 71.85; 65.087		693.02Seo, Boram; Kim, Ya Gob; Lee, Phil Ho
Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles.
Organic letters, 2016, 18, 5050-5053
1555794 CIFC18 H14 Br N O2 SP -19.5374; 9.5911; 9.782
102.386; 108.954; 91.485		822.15Seo, Boram; Kim, Ya Gob; Lee, Phil Ho
Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles.
Organic letters, 2016, 18, 5050-5053
1555795 CIFC66 H62 Cl6 N4P 1 21/c 116.487; 19.2778; 18.1092
90; 101.874; 90		5632.5Zhu, Huangtianzhi; Shi, Bingbing; Chen, Kexian; Wei, Peifa; Xia, Danyu; Mondal, Julfikar Hassan; Huang, Feihe
Cyclo[4]carbazole, an Iodide Anion Macrocyclic Receptor.
Organic letters, 2016, 18, 5054-5057
1555796 CIFC64 H60 N4R -3 :H31.6291; 31.6291; 12.7824
90; 90; 120		11074.3Zhu, Huangtianzhi; Shi, Bingbing; Chen, Kexian; Wei, Peifa; Xia, Danyu; Mondal, Julfikar Hassan; Huang, Feihe
Cyclo[4]carbazole, an Iodide Anion Macrocyclic Receptor.
Organic letters, 2016, 18, 5054-5057
1555797 CIFC18 H15 N O3P 1 21/n 17.9712; 7.3926; 23.378
90; 94.406; 90		1373.5Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin
Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones.
Organic letters, 2016, 18, 5232-5235
1555798 CIFC17 H13 N O2P -18.338; 8.477; 9.528
93.456; 101.166; 104.331		636Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin
Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones.
Organic letters, 2016, 18, 5232-5235
1555799 CIFC15 H9 N OP n a 2114.933; 5.3922; 25.637
90; 90; 90		2064.3Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin
Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones.
Organic letters, 2016, 18, 5232-5235
1555800 CIFC17 H13 N OP 21 21 217.2723; 12.1743; 13.9939
90; 90; 90		1239Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin
Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones.
Organic letters, 2016, 18, 5232-5235
1555801 CIFC21 H17 Br O2P 21 21 218.2974; 13.684; 15.775
90; 90; 90		1791.12Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min
Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach.
Organic letters, 2016, 18, 4754-4757
1555802 CIFC21 H16 Cl2 O2P 1 21/n 110.0284; 17.8821; 10.2286
90; 98.735; 90		1813.01Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min
Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach.
Organic letters, 2016, 18, 4754-4757
1555803 CIFC21 H16 Cl2 O2P -17.5712; 8.8981; 14.6818
76.585; 82.407; 74.099		922.81Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min
Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach.
Organic letters, 2016, 18, 4754-4757
1555804 CIFC25 H18 N2P -110.098; 12.6554; 15.8728
103.793; 91.637; 111.127		1822.8Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan
Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation.
Organic letters, 2016, 18, 5066-5069
1555805 CIFC20 H16 N2P 1 21/c 111.17; 16.077; 8.4209
90; 108.359; 90		1435.3Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan
Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation.
Organic letters, 2016, 18, 5066-5069
1555806 CIFC25 H16 N2P 1 21/n 111.1107; 9.7397; 15.8289
90; 101.488; 90		1678.6Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan
Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation.
Organic letters, 2016, 18, 5066-5069
1555807 CIFC19 H20 N2 O3P b c a10.6778; 15.1304; 20.376
90; 90; 90		3291.9Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan
Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation.
Organic letters, 2016, 18, 5066-5069
1555808 CIFC24 H19 F N2 O3P 21 21 215.86821; 16.6995; 20.8172
90; 90; 90		2040.01Guo, Songsong; Liu, Xiaohua; Shen, Bin; Lin, Lili; Feng, Xiaoming
Organocatalytic Asymmetric Cascade Reaction of 2-Hydroxyphenyl-Substituted Enones and Isocyanates To Construct 1,3-Benzoxazin-2-ones.
Organic letters, 2016, 18, 5070-5073
1555809 CIFC23 H22 Cl N O3 SP -112.179; 12.639; 15.612
95.437; 101.771; 115.319		2081.2Yabuuchi, Yuto; Kuzuguchi, Takeo; Yoshimura, Tomoyuki; Matsuo, Jun-Ichi
Synthesis of α-Halo-γ-hydroxyenamides by Titanium Tetrahalide Mediated Addition of Aldehydes or Ketones to Ynamides.
Organic letters, 2016, 18, 4951-4953
1555810 CIFC17 H18 Cl N O2 SC 1 2/c 130.1678; 8.0311; 14.2794
90; 100.975; 90		3396.4Yabuuchi, Yuto; Kuzuguchi, Takeo; Yoshimura, Tomoyuki; Matsuo, Jun-Ichi
Synthesis of α-Halo-γ-hydroxyenamides by Titanium Tetrahalide Mediated Addition of Aldehydes or Ketones to Ynamides.
Organic letters, 2016, 18, 4951-4953
1555811 CIFC35 H31 N7P 1 21/c 119.24; 21.296; 14.917
90; 111.847; 90		5673Liu, Yang; Long, Chao; Zhao, Liang; Wang, Mei-Xiang
Functionalization of Azacalixaromatics by Cu(II)-Catalyzed Oxidative Cross-Coupling Reaction between the Arene C-H Bond and Boronic Acids.
Organic letters, 2016, 18, 5078-5081
1555812 CIFC35 H31 N7P 1 21/c 117.296; 10.5965; 15.8781
90; 101.794; 90		2848.7Liu, Yang; Long, Chao; Zhao, Liang; Wang, Mei-Xiang
Functionalization of Azacalixaromatics by Cu(II)-Catalyzed Oxidative Cross-Coupling Reaction between the Arene C-H Bond and Boronic Acids.
Organic letters, 2016, 18, 5078-5081
1555813 CIFC27 H23 N O4 SP 1 21/n 19.3674; 22.177; 11.7
90; 106.835; 90		2326.4Guo, Songjin; Yuan, Kai; Gu, Meng; Lin, Aijun; Yao, Hequan
Rh(III)-Catalyzed Cascade Annulation/C-H Activation of o-Ethynylanilines with Diazo Compounds: One-Pot Synthesis of Benzo[a]carbazoles via 1,4-Rhodium Migration.
Organic letters, 2016, 18, 5236-5239
1555814 CIFC27 H24 O S2P -19.7091; 10.2062; 12.3
79.629; 69.436; 72.515		1084.7Liang, Yongping; Lai, Junshan; Liu, Teng; Tang, Shouchu
Direct Regioselective [3 + 2]-Cyclization Reactions of Ambivalent Electrophilic/Nucleophilic β-Chlorovinyl Dithianes: Access to Cyclopentene Derivatives.
Organic letters, 2016, 18, 5086-5089
1555815 CIFC27 H24 O S2P 1 21/n 115.4129; 9.30538; 15.704
90; 99.233; 90		2223.13Liang, Yongping; Lai, Junshan; Liu, Teng; Tang, Shouchu
Direct Regioselective [3 + 2]-Cyclization Reactions of Ambivalent Electrophilic/Nucleophilic β-Chlorovinyl Dithianes: Access to Cyclopentene Derivatives.
Organic letters, 2016, 18, 5086-5089
1555816 CIFC20 H17 Cl O4P 1 21/c 16.2163; 23.306; 11.8875
90; 96.96; 90		1709.5Zhang, Ming-Liang; Wu, Zhi-Jun; Zhao, Jian-Qiang; Luo, Yuan; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng
Michael Addition-Lactonization of Arylacetyl Phosphonate to β,γ-Unsaturated α-Keto Esters for the Synthesis of Chiral syn-3,4-Dihydropyranones and 5,6-Dihydropyranones.
Organic letters, 2016, 18, 5110-5113
1555817 CIFC19 H15 Br O4P 21 21 216.86; 10.8272; 22.448
90; 90; 90		1667.3Zhang, Ming-Liang; Wu, Zhi-Jun; Zhao, Jian-Qiang; Luo, Yuan; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng
Michael Addition-Lactonization of Arylacetyl Phosphonate to β,γ-Unsaturated α-Keto Esters for the Synthesis of Chiral syn-3,4-Dihydropyranones and 5,6-Dihydropyranones.
Organic letters, 2016, 18, 5110-5113
1555818 CIFC29 H23 O2 P SeP 2 21 217.4297; 13.2923; 23.557
90; 90; 90		2326.4Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki
Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom.
Organic letters, 2016, 18, 5264-5267
1555819 CIFC30 H25 O2 P SeP 21 21 217.48; 16.779; 19.319
90; 90; 90		2424.7Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki
Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom.
Organic letters, 2016, 18, 5264-5267
1555820 CIFC36 H27 O4 P SeP 21 21 2111.8545; 15.6874; 16.0313
90; 90; 90		2981.3Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki
Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom.
Organic letters, 2016, 18, 5264-5267
1555821 CIFC21 H22 O5P 1 21 18.4714; 6.2472; 17.1326
90; 101.606; 90		888.16Akula, Ramulu; Guiry, Patrick J.
Enantioselective Synthesis of α-Allyl-α-aryldihydrocoumarins and 3-Isochromanones via Pd-Catalyzed Decarboxylative Asymmetric Allylic Alkylation.
Organic letters, 2016, 18, 5472-5475
1555822 CIFC21 H18 O2P b c a7.5079; 14.0053; 29.564
90; 90; 90		3108.7Li, Deng Yuan; Jiang, Liang Liang; Chen, Shuang; Huang, Zheng Lu; Dang, Li; Wu, Xin Yan; Liu, Pei Nian
Cascade Reaction of Alkynols and 7-Oxabenzonorbornadienes Involving Transient Hemiketal Group Directed C-H Activation and Synergistic Rh<sup>III</sup>/Sc<sup>III</sup> Catalysis.
Organic letters, 2016, 18, 5134-5137
1555823 CIFC23 H21 Br2 N2 OP 1 21/c 116.6039; 12.5136; 9.0084
90; 101.188; 90		1836.1Lin, Dongqing; Wei, Ying; Ou, Changjin; Huang, Hao; Xie, Linghai; Tang, Lei; Huang, Wei
Carbon Cationic Relay via Superelectrophiles: Synthesis of Spiro-diazafluorenes.
Organic letters, 2016, 18, 6220-6223
1555824 CIFC27 H28 O9 SP -19.7672; 11.7742; 24.7073
101.224; 93.188; 112.05		2557.16Huang, Lin; Ye, Liu; Li, Xiao-Hua; Li, Zhong-Liang; Lin, Jin-Shun; Liu, Xin-Yuan
Stereoselective Radical Cyclization Cascades Triggered by Addition of Diverse Radicals to Alkynes To Construct 6(5)-6-5 Fused Rings.
Organic letters, 2016, 18, 5284-5287
1555825 CIFC16 H10 Br F3 N2 OP -16.9696; 7.0783; 16.56
101.962; 93.626; 94.073		794.6Huang, Lin; Ye, Liu; Li, Xiao-Hua; Li, Zhong-Liang; Lin, Jin-Shun; Liu, Xin-Yuan
Stereoselective Radical Cyclization Cascades Triggered by Addition of Diverse Radicals to Alkynes To Construct 6(5)-6-5 Fused Rings.
Organic letters, 2016, 18, 5284-5287
1555826 CIFC18 H14 O3P 17.6607; 9.2315; 11.127
72.019; 79.887; 74.428		717.29Zhu, Gongming; Bao, Guangjun; Li, Yiping; Yang, Junxian; Sun, Wangsheng; Li, Jing; Hong, Liang; Wang, Rui
Chiral Phosphoric Acid Catalyzed Asymmetric Oxidative Dearomatization of Naphthols with Quinones.
Organic letters, 2016, 18, 5288-5291
1555827 CIFC23 H15 N OP 1 21/n 18.542; 10.786; 18.502
90; 102.652; 90		1663.3Zhang, Fangfang; Qin, Zhengchen; Kong, Lingkai; Zhao, Yulei; Liu, Yuanyuan; Li, Yanzhong
Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o-Alkynyl)phenyl Enaminones: Synthesis of α-Naphthylamines and Indeno[1,2-c]pyrrolones.
Organic letters, 2016, 18, 5150-5153
1555828 CIFC23 H17 N OP -18.369; 9.476; 11.907
108.133; 106.771; 92.352		850.3Zhang, Fangfang; Qin, Zhengchen; Kong, Lingkai; Zhao, Yulei; Liu, Yuanyuan; Li, Yanzhong
Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o-Alkynyl)phenyl Enaminones: Synthesis of α-Naphthylamines and Indeno[1,2-c]pyrrolones.
Organic letters, 2016, 18, 5150-5153
1555829 CIFC18 H14 N2 O4C 1 c 15.5545; 22.3478; 25.462
90; 94.477; 90		3151Meng, Ling-Hong; Wang, Chen-Yin; Mándi, Attila; Li, Xiao-Ming; Hu, Xue-Yi; Kassack, Matthias U.; Kurtán, Tibor; Wang, Bin-Gui
Three Diketopiperazine Alkaloids with Spirocyclic Skeletons and One Bisthiodiketopiperazine Derivative from the Mangrove-Derived Endophytic Fungus Penicillium brocae MA-231.
Organic letters, 2016, 18, 5304-5307
1555830 CIFC18 H20 O7P 1 21 16.7535; 10.0644; 12.3488
90; 91.205; 90		839.16Shi, Yunlong; Pierce, Joshua G.
Stereocontrolled Synthesis of (+)-Plagiogyrin A.
Organic letters, 2016, 18, 5308-5311
1555831 CIFC18 H20 O7P -18.8256; 9.3741; 10.7509
69.044; 81.513; 81.953		817.85Shi, Yunlong; Pierce, Joshua G.
Stereocontrolled Synthesis of (+)-Plagiogyrin A.
Organic letters, 2016, 18, 5308-5311
1555832 CIFC25 H30 N2 O9P -19.4188; 11.1969; 12.4356
101.95; 109.822; 95.373		1187.75Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555833 CIFC22 H21 N O5P -18.5998; 9.2091; 13.2372
84.15; 72.472; 64.512		901.91Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555834 CIFC9 H6 O5P 1 c 17.26017; 9.48057; 11.4368
90; 91.943; 90		786.75Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555835 CIFC15 H21 N O5P -18.8765; 9.1065; 9.7523
96.026; 90.185; 110.137		735.38Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555836 CIFC8 H5 Cl O3C 1 2/c 112.8414; 7.46056; 15.3814
90; 101.17; 90		1445.69Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555837 CIFC35 H34 N2 O5P 1 21/n 19.36155; 12.6426; 22.9131
90; 90.3246; 90		2711.82Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555838 CIFC34 H33 Cl N2 O3P 21 21 217.61287; 18.37433; 18.9503
90; 90; 90		2650.79Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555839 CIFC21 H20 Cl N O3P -18.3659; 8.5097; 13.3207
108.425; 106.74; 90.498		856.37Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555840 CIFC35 H40 N2 O8P -19.6296; 11.8041; 14.0277
96.799; 105.982; 92.907		1516.29Dwight, Stephen J.; Levin, Sergiy
Scalable Regioselective Synthesis of Rhodamine Dyes.
Organic letters, 2016, 18, 5316-5319
1555841 CIFC12 H13 N2 O SP 1 21/c 15.8328; 14.6676; 14.1401
90; 106.475; 90		1160.06Andeme Edzang, Judicaelle; Chen, Zhongrui; Audi, Hassib; Canard, Gabriel; Siri, Olivier
Transamination at the Crossroad of the One-Pot Synthesis of N-Substituted Quinonediimines and C-Substituted Benzobisimidazoles.
Organic letters, 2016, 18, 5340-5343
1555842 CIFC11 H20 N2P -16.5009; 8.0222; 11.3792
85.438; 77.389; 72.879		553.39Andeme Edzang, Judicaelle; Chen, Zhongrui; Audi, Hassib; Canard, Gabriel; Siri, Olivier
Transamination at the Crossroad of the One-Pot Synthesis of N-Substituted Quinonediimines and C-Substituted Benzobisimidazoles.
Organic letters, 2016, 18, 5340-5343
1555843 CIFC25 H24 O4P 1 21/n 18.8495; 15.8052; 14.3121
90; 95.864; 90		1991.3Gratia, Synthia; Mosesohn, Kathryn; Diver, Steven T.
Highly Selective Ring Expansion of Bicyclo[3.1.0]hexenes.
Organic letters, 2016, 18, 5320-5323
1555844 CIFC21 H22 N2P -18.8501; 9.6086; 10.7805
74.645; 86.219; 69.215		826.09Song, Runzhe; Han, Zhaomeng; He, Qiuqin; Fan, Renhua
Amine-Mediated Transimination and Aromatization-Triggered Domino Reaction in the Synthesis of Polyfunctionalized 4-Aminoquinolines.
Organic letters, 2016, 18, 5328-5331
1555845 CIFC14 H16 O2P 1 21/n 18.5881; 15.4507; 8.7345
90; 99.603; 90		1142.76Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555846 CIFC22 H22 O7P c a 2115.8269; 5.82087; 20.8138
90; 90; 90		1917.5Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555847 CIFC13 H14 O2P 1 21/n 16.8052; 10.2396; 15.216
90; 100.317; 90		1043.15Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555848 CIFC14 H14 O2P b c a14.9062; 8.6079; 17.2918
90; 90; 90		2218.7Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555849 CIFC16 H22 O4P 1 21/c 125.983; 5.7576; 10.4224
90; 100.35; 90		1533.8Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555850 CIFC12 H12 O2P 1 21/n 18.27; 8.534; 13.743
90; 90.047; 90		969.9Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen
Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.
Organic letters, 2016, 18, 5170-5173
1555851 CIFC15 H15 N O3P -17.236; 8.5114; 11.77
107.206; 104.236; 99.256		649.5Lanke, Veeranjaneyulu; Bettadapur, Kiran R.; Prabhu, Kandikere Ramaiah
Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles.
Organic letters, 2016, 18, 5496-5499
1555852 CIFC15 H12 F3 N O3C 1 c 128.703; 13.0666; 8.1548
90; 106.279; 90		2935.8Lanke, Veeranjaneyulu; Bettadapur, Kiran R.; Prabhu, Kandikere Ramaiah
Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles.
Organic letters, 2016, 18, 5496-5499
1555853 CIFC23 H23 N O7 SP 1 21/c 112.0449; 17.559; 11.278
90; 105.674; 90		2296.56Yuan, Hao; Gong, Jianxian; Yang, Zhen
Stereoselective Synthesis of Oxabicyclo[2.2.1]heptenes via a Tandem Dirhodium(II)-Catalyzed Triazole Denitrogenation and [3 + 2] Cycloaddition.
Organic letters, 2016, 18, 5500-5503
1555854 CIFC28 H31 N O7 SP 1 21/c 116.125; 19.416; 9.015
90; 102.099; 90		2759.7Yuan, Hao; Gong, Jianxian; Yang, Zhen
Stereoselective Synthesis of Oxabicyclo[2.2.1]heptenes via a Tandem Dirhodium(II)-Catalyzed Triazole Denitrogenation and [3 + 2] Cycloaddition.
Organic letters, 2016, 18, 5500-5503
1555855 CIFC21 H23 N O3 SP 1 21/n 110.264; 17.364; 21.635
90; 93.165; 90		3850Yuan, Hao; Gong, Jianxian; Yang, Zhen
Stereoselective Synthesis of Oxabicyclo[2.2.1]heptenes via a Tandem Dirhodium(II)-Catalyzed Triazole Denitrogenation and [3 + 2] Cycloaddition.
Organic letters, 2016, 18, 5500-5503
1555856 CIFC21 H16 N2 OP -17.5003; 8.43; 12.7367
91.619; 101.145; 98.005		781.16Stephens, David E.; Nguyen, Vu T.; Chhetri, Bhuwan; Clark, Emily R.; Arman, Hadi D.; Larionov, Oleg V.
Organocatalytic Synthesis of Methylene-Bridged N-Heterobiaryls.
Organic letters, 2016, 18, 5808-5811
1555857 CIFC20 H15 N3P 1 21/n 19.2699; 17.2089; 10.2868
90; 104.856; 90		1586.14Lamb, Alan D.; Davey, Peter D.; Driver, Russell W.; Thompson, Amber L.; Smith, Martin D.
Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization.
Organic letters, 2016, 18, 5372-5375
1555858 CIFC20 H15 N3P 1 21/a 111.6533; 10.6806; 13.6153
90; 109.726; 90		1595.18Lamb, Alan D.; Davey, Peter D.; Driver, Russell W.; Thompson, Amber L.; Smith, Martin D.
Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization.
Organic letters, 2016, 18, 5372-5375
1555859 CIFC21 H23 Br N2 O4P 21 21 2112.2019; 15.5905; 21.6362
90; 90; 90		4115.93Lamb, Alan D.; Davey, Peter D.; Driver, Russell W.; Thompson, Amber L.; Smith, Martin D.
Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization.
Organic letters, 2016, 18, 5372-5375
1555860 CIFC116 H122 B2 F4 N8 O6P -4 21 c32.715; 32.715; 20.819
90; 90; 90		22282Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555861 CIFC85 H80 N6 O3P 1 21/c 124.962; 19.0061; 15.2293
90; 104.651; 90		6990.3Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555862 CIFC104 H96 N8 O4C 1 2/c 150.36; 16.491; 26.798
90; 119.019; 90		19461Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555863 CIFC130 H115 N10 O5P -114.8093; 20.899; 23.578
85.057; 76.172; 73.381		6788.6Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555864 CIFC84 H77 B3 Cl6 F6 N8 O3P 1 21/n 114.2376; 19.4354; 29.2846
90; 97.352; 90		8036.8Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555865 CIFC104 H92 B4 F8 N8 O4I -422.2417; 22.2417; 12.1892
90; 90; 90		6029.9Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555866 CIFC52 H48 N4 O2C 1 2/c 120.228; 10.5483; 18.6443
90; 92.898; 90		3973.1Uchida, Junji; Nakamura, Takashi; Yamamura, Masaki; Yamaguchi, Gento; Nabeshima, Tatsuya
m-Phenylene-Linked Dipyrrins and Their Boron-Difluoride Complexes as Variously Shaped Macrocyclic Oligomers.
Organic letters, 2016, 18, 5380-5383
1555867 CIFC17 H18 Cl N O2 SP 21 21 218.072; 12.922; 15.704
90; 90; 90		1638Song, Guangjun; Zheng, Ziwei; Wang, Yanhui; Yu, Xinhong
Pd-Catalyzed Site-Selective p-Hydroxyphenyloxylation of Benzylic α-C(sp<sup>3</sup>)-H Bonds with 1,4-Benzoquinone.
Organic letters, 2016, 18, 6002-6005
1555868 CIFC90.5 H69 Br4 Cl5 N4 O8 S4C 2 2 2120.4233; 28.5691; 33.289
90; 90; 90		19423Arai, Takayoshi; Miyazaki, Tomoya; Ogawa, Hiroki; Masu, Hyuma
PyBidine-Ni(OAc)<sub>2</sub>-Catalyzed Michael/Aldol Reaction of Methyleneindolinones and Thiosalicylaldehydes for Stereochemically Divergent Thiochromanyl-spirooxindoles.
Organic letters, 2016, 18, 5824-5827
1555869 CIFC22 H21 Cl N O2P 21 21 216.01931; 16.3547; 19.4786
90; 90; 90		1917.55Guo, Jing; Lin, Lili; Liu, Yangbin; Li, Xiangqiang; Liu, Xiaohua; Feng, Xiaoming
Nickel(II)-Catalyzed Enantioselective α-Vinylation of β-Keto Amides/Esters with Hypervalent Iodine Salts.
Organic letters, 2016, 18, 5540-5543
1555870 CIFC20 H21 N O2P 17.0663; 8.3624; 8.9048
115.442; 109.848; 92.591		435.48Guo, Jing; Lin, Lili; Liu, Yangbin; Li, Xiangqiang; Liu, Xiaohua; Feng, Xiaoming
Nickel(II)-Catalyzed Enantioselective α-Vinylation of β-Keto Amides/Esters with Hypervalent Iodine Salts.
Organic letters, 2016, 18, 5540-5543
1555871 CIFC142 H123 Cl8 Cu10 I10 N18 O12P 1 21 116.7926; 23.6471; 19.7202
90; 91.4006; 90		7828.5Dasgupta, Srimoyee; Liu, Jixin; Shoffler, Clarissa A.; Yap, Glenn P. A.; Watson, Mary P.
Enantioselective, Copper-Catalyzed Alkynylation of Ketimines To Deliver Isoquinolines with α-Diaryl Tetrasubstituted Stereocenters.
Organic letters, 2016, 18, 6006-6009
1555872 CIFC25 H19 N O2P 1 21 18.7464; 9.4368; 11.5501
90; 93.365; 90		951.68Dasgupta, Srimoyee; Liu, Jixin; Shoffler, Clarissa A.; Yap, Glenn P. A.; Watson, Mary P.
Enantioselective, Copper-Catalyzed Alkynylation of Ketimines To Deliver Isoquinolines with α-Diaryl Tetrasubstituted Stereocenters.
Organic letters, 2016, 18, 6006-6009
1555873 CIFC44 H76 Cd2 Cl8 N24 O23P -112.5479; 12.643; 13.1867
62.564; 77.54; 80.141		1806.7Shen, Fang-Fang; Chen, Kai; Zhang, Yun-Qian; Zhu, Qian-Jiang; Tao, Zhu; Cong, Hang
Mono- and Dihydroxylated Symmetrical Octamethylcucurbiturils and Allylated Derivatives.
Organic letters, 2016, 18, 5544-5547
1555874 CIFC66 H138 N36 O51P -112.4005; 12.7258; 34.039
83.66; 83.95; 82.86		5274.4Shen, Fang-Fang; Chen, Kai; Zhang, Yun-Qian; Zhu, Qian-Jiang; Tao, Zhu; Cong, Hang
Mono- and Dihydroxylated Symmetrical Octamethylcucurbiturils and Allylated Derivatives.
Organic letters, 2016, 18, 5544-5547
1555875 CIFC32 H26 N2 O5P -18.4386; 10.3727; 15.076
104.374; 91.345; 102.817		1242.1Dighe, Shashikant U.; Yadav, Veena D.; Mahar, Rohit; Shukla, Sanjeev K.; Batra, Sanjay
Intramolecular C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>2</sup></sub> Friedel-Crafts Arylation: Substrate- and Condition-Controlled Divergent Synthesis of Fused-β-carbolines.
Organic letters, 2016, 18, 6010-6013
1555876 CIFC19 H17 Br O2 SP b c a14.8765; 9.6372; 24.3534
90; 90; 90		3491.5Son, Jeong-Yu; Kim, Jonghye; Han, Sang Hoon; Kim, Sung Hong; Lee, Phil Ho
Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Alkenes.
Organic letters, 2016, 18, 5408-5411
1555877 CIFC32 H20 O4 S2P 1 21/n 19.7687; 18.1178; 16.7748
90; 103.668; 90		2884.85Son, Jeong-Yu; Kim, Jonghye; Han, Sang Hoon; Kim, Sung Hong; Lee, Phil Ho
Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Alkenes.
Organic letters, 2016, 18, 5408-5411
1555878 CIFC17 H24 O2 S SiP 1 21/c 110.1244; 18.7208; 9.5787
90; 91.3035; 90		1815.05Son, Jeong-Yu; Kim, Jonghye; Han, Sang Hoon; Kim, Sung Hong; Lee, Phil Ho
Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Alkenes.
Organic letters, 2016, 18, 5408-5411
1555879 CIFC25 H19 N O2P -16.38; 11.8204; 13.095
96.666; 95.878; 102.772		948.2Chen, Zi-Sheng; Yang, Fang; Ling, Huibo; Li, Mengxue; Gao, Jin-Ming; Ji, Kegong
Metal-Free, Site-Selective Addition to Ynones: An Approach to Synthesize Substituted Quinoline Derivatives.
Organic letters, 2016, 18, 5828-5831
1555880 CIFC31 H21 N O2P -19.247; 10.736; 12.601
74.29; 78.02; 74.27		1146.9Chen, Zi-Sheng; Yang, Fang; Ling, Huibo; Li, Mengxue; Gao, Jin-Ming; Ji, Kegong
Metal-Free, Site-Selective Addition to Ynones: An Approach to Synthesize Substituted Quinoline Derivatives.
Organic letters, 2016, 18, 5828-5831
1555881 CIFC28 H30 Br N O5P 1 21/n 18.303; 17.7016; 17.5144
90; 99.293; 90		2540.42Das, Saikat; Daniliuc, Constantin G.; Studer, Armido
Multicomponent 1,3-Bifunctionalization of Donor-Acceptor Cyclopropanes with Arenes and Nitrosoarenes.
Organic letters, 2016, 18, 5576-5579
1555882 CIFC15 H15 N O4P 21 21 218.5631; 11.52249; 13.97167
90; 90; 90		1378.56Cao, Yang; Zhang, Xiang; Lin, Guangyu; Zhang-Negrerie, Daisy; Du, Yunfei
Chiral Aryliodine-Mediated Enantioselective Organocatalytic Spirocyclization: Synthesis of Spirofurooxindoles via Cascade Oxidative C-O and C-C Bond Formation.
Organic letters, 2016, 18, 5580-5583
1555883 CIFC14 H13 N O4P 1 21/c 19.625; 16.95; 8.295
90; 114.355; 90		1232.8Cao, Yang; Zhang, Xiang; Lin, Guangyu; Zhang-Negrerie, Daisy; Du, Yunfei
Chiral Aryliodine-Mediated Enantioselective Organocatalytic Spirocyclization: Synthesis of Spirofurooxindoles via Cascade Oxidative C-O and C-C Bond Formation.
Organic letters, 2016, 18, 5580-5583
1555884 CIFC11 H12 O2P 21 21 216.9549; 10.5071; 12.9403
90; 90; 90		945.62Rastelli, Ettore J.; Truong, Ngoc T.; Coltart, Don M.
Asymmetric Induction in Hydroacylation by Cooperative Iminium Ion-Transition-Metal Catalysis.
Organic letters, 2016, 18, 5588-5591
1555885 CIFC11 H13 Br O3C 1 2 119.301; 5.7434; 12.35
90; 120.282; 90		1182.2Hou, Chuan-Jin; Hu, Xiang-Ping
Sterically Hindered Chiral Ferrocenyl P,N,N-Ligands for Highly Diastereo-/Enantioselective Ir-Catalyzed Hydrogenation of α-Alkyl-β-ketoesters via Dynamic Kinetic Resolution.
Organic letters, 2016, 18, 5592-5595
1555886 CIFC36 H34 Fe N2 PP 1 21 110.7641; 11.7191; 11.5933
90; 95.782; 90		1455Hou, Chuan-Jin; Hu, Xiang-Ping
Sterically Hindered Chiral Ferrocenyl P,N,N-Ligands for Highly Diastereo-/Enantioselective Ir-Catalyzed Hydrogenation of α-Alkyl-β-ketoesters via Dynamic Kinetic Resolution.
Organic letters, 2016, 18, 5592-5595
1555887 CIFC19 H24 N2P 1 21/n 113.6186; 6.4135; 17.071
90; 97.35; 90		1478.78Koovits, Paul J.; Knowles, Jonathan P.; Booker-Milburn, Kevin I
Conformationally Driven Two- and Three-Photon Cascade Processes in the Stereoselective Photorearrangement of Pyrroles.
Organic letters, 2016, 18, 5608-5611
1555888 CIFC10 H13 N O2P -18.0081; 10.4609; 11.1597
78.2095; 78.146; 81.6257		890.37Koovits, Paul J.; Knowles, Jonathan P.; Booker-Milburn, Kevin I
Conformationally Driven Two- and Three-Photon Cascade Processes in the Stereoselective Photorearrangement of Pyrroles.
Organic letters, 2016, 18, 5608-5611
1555889 CIFC39 H36 O3P 1 21/n 115.9124; 10.2339; 19.2806
90; 108.253; 90		2981.78Ye, Fei; Haddad, Mansour; Michelet, Véronique; Ratovelomanana-Vidal, Virginie
Access toward Fluorenone Derivatives through Solvent-Free Ruthenium Trichloride Mediated [2 + 2 + 2] Cycloadditions.
Organic letters, 2016, 18, 5612-5615
1555890 CIFC16 H14 F3 N O2P 1 21/c 18.0461; 17.462; 10.6706
90; 96.238; 90		1490.4Bhojgude, Sachin Suresh; Roy, Tony; Gonnade, Rajesh G.; Biju, Akkattu T.
Substrate-Controlled Selectivity Switch in the Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and CO<sub>2</sub>.
Organic letters, 2016, 18, 5424-5427
1555891 CIFC30 H30 N P SP 1 21/c 116.799; 16.6108; 19.616
90; 108.792; 90		5182Unoh, Yuto; Yokoyama, Yuki; Satoh, Tetsuya; Hirano, Koji; Miura, Masahiro
Regioselective Synthesis of Benzo[b]phosphole Derivatives via Direct ortho-Alkenylation and Cyclization of Arylthiophosphinamides.
Organic letters, 2016, 18, 5436-5439
1555892 CIFC31 H31 F3 N O3 P S2P n a 2119.87; 16.3; 8.985
90; 90; 90		2910Unoh, Yuto; Yokoyama, Yuki; Satoh, Tetsuya; Hirano, Koji; Miura, Masahiro
Regioselective Synthesis of Benzo[b]phosphole Derivatives via Direct ortho-Alkenylation and Cyclization of Arylthiophosphinamides.
Organic letters, 2016, 18, 5436-5439
1555893 CIFC20 H17 Fe NP b c a18.249; 7.4323; 22.242
90; 90; 90		3016.7Zhou, Shuguang; Wang, Mingyang; Wang, Lili; Chen, Kehao; Wang, Jinhu; Song, Chao; Zhu, Jin
Bidentate Directing-Enabled, Traceless Heterocycle Synthesis: Cobalt-Catalyzed Access to Isoquinolines.
Organic letters, 2016, 18, 5632-5635
1555894 CIFC29 H25 F N2 O2P -19.0735; 11.257; 11.893
91.917; 90.265; 99.335		1197.9Song, Zhidong; Huang, Xin; Yi, Wenbin; Zhang, Wei
One-Pot Reactions for Modular Synthesis of Polysubstituted and Fused Pyridines.
Organic letters, 2016, 18, 5640-5643
1555895 CIFC16 H12 O3 SP 21 21 216.4113; 10.0776; 20.2079
90; 90; 90		1305.64Vila, Carlos; Quintero, Lucia; Blay, Gonzalo; Muñoz, M Carmen; Pedro, José R
Organocatalytic Enantioselective Synthesis of α-Hydroxyketones through a Friedel-Crafts Reaction of Naphthols and Activated Phenols with Aryl- and Alkylglyoxal Hydrates.
Organic letters, 2016, 18, 5652-5655
1555896 CIFC145 H144 N4 O5 Pt2 S32P -115.954; 16.992; 17.29
107.17; 114.97; 94.23		3951.8Bastien, Guillaume; Dron, Paul I.; Vincent, Manon; Canevet, David; Allain, Magali; Goeb, Sébastien; Sallé, Marc
C<sub>60</sub> Recognition from Extended Tetrathiafulvalene Bis-acetylide Platinum(II) Complexes.
Organic letters, 2016, 18, 5856-5859
1555897 CIFC24 H17 F2 N OP 21 21 218.4273; 9.8386; 22.562
90; 90; 90		1870.7Fujino, Takumi; Hinoue, Tomoaki; Usuki, Yoshinosuke; Satoh, Tetsuya
Synthesis of Difluorinated Enynes through Sonogashira-Type Coupling.
Organic letters, 2016, 18, 5688-5691
1555898 CIFC18 H10 F2P 1 21/c 18.5766; 19.0076; 7.8189
90; 92.3; 90		1273.6Fujino, Takumi; Hinoue, Tomoaki; Usuki, Yoshinosuke; Satoh, Tetsuya
Synthesis of Difluorinated Enynes through Sonogashira-Type Coupling.
Organic letters, 2016, 18, 5688-5691
1555899 CIFC29 H21 N O3 S2P -19.995; 15.594; 17.952
76.027; 81.673; 77.58		2638.9Dong, Yu-Ting; Jin, Quan; Zhou, Ling; Chen, Jie
N-Heterocyclic Carbene Catalyzed Sulfenylation of α,β-Unsaturated Aldehydes.
Organic letters, 2016, 18, 5708-5711
1555900 CIFC63 H43 S16P -112.31; 14.356; 18.752
82.396; 76.856; 70.392		3034Ogi, Daisuke; Fujita, Yusuke; Mori, Shigeki; Shirahata, Takashi; Misaki, Yohji
Bis- and Tris-fused Tetrathiafulvalenes Extended with Anthracene-9,10-diylidene.
Organic letters, 2016, 18, 5868-5871
1555901 CIFC30 H32P -18.9306; 9.8068; 14.0936
74.745; 85.237; 87.353		1186.34Kanno, Ken-Ichiro; Igarashi, Eri; Mizukami, Yuki; Nakajima, Kiyohiko; Song, Zhiyi; Takahashi, Tamotsu
Formation of Seven-Membered Carbocycles via 7-endo Mode Cyclization of Lithioheptatrienes.
Organic letters, 2016, 18, 6217-6219
1555902 CIFC23 H26P -16.13; 9.435; 17.3238
79.085; 82.396; 67.34		905.93Kanno, Ken-Ichiro; Igarashi, Eri; Mizukami, Yuki; Nakajima, Kiyohiko; Song, Zhiyi; Takahashi, Tamotsu
Formation of Seven-Membered Carbocycles via 7-endo Mode Cyclization of Lithioheptatrienes.
Organic letters, 2016, 18, 6217-6219
1555903 CIFC14 H13 Br O3P 1 21/c 115.1061; 6.2721; 15.7059
90; 114.169; 90		1357.6Chen, Zi-Sheng; Huang, Xiao-Yan; Gao, Jin-Ming; Ji, Kegong
Relay Rh(II)/Pd(0) Dual Catalysis: Selective Construction of Cyclic All-Quaternary Carbon Centers.
Organic letters, 2016, 18, 5876-5879
1555904 CIFC21 H19 N O5C 1 2/c 124.915; 10.604; 15.39
90; 113.315; 90		3734Chen, Zi-Sheng; Huang, Xiao-Yan; Gao, Jin-Ming; Ji, Kegong
Relay Rh(II)/Pd(0) Dual Catalysis: Selective Construction of Cyclic All-Quaternary Carbon Centers.
Organic letters, 2016, 18, 5876-5879
1555905 CIFC23 H33 F6 N O4P -18.6692; 9.105; 15.8619
93.843; 91.883; 99.166		1232.06Colomer, Ignacio; Barcelos, Rosimeire Coura; Christensen, Kirsten E.; Donohoe, Timothy J.
Orthogonally Protected 1,2-Diols from Electron-Rich Alkenes Using Metal-Free Olefin syn-Dihydroxylation.
Organic letters, 2016, 18, 5880-5883
1555906 CIFC21 H33 N O4P 1 21/n 110.7863; 8.519; 22.5231
90; 94.7132; 90		2062.62Colomer, Ignacio; Barcelos, Rosimeire Coura; Christensen, Kirsten E.; Donohoe, Timothy J.
Orthogonally Protected 1,2-Diols from Electron-Rich Alkenes Using Metal-Free Olefin syn-Dihydroxylation.
Organic letters, 2016, 18, 5880-5883
1555907 CIFC16 H13 N3 OP 1 21/c 111.326; 12.672; 9.2889
90; 94.75; 90		1328.6Wan, Jie-Ping; Cao, Shuo; Liu, Yunyun
Base-Promoted Synthesis of N-Substituted 1,2,3-Triazoles via Enaminone-Azide Cycloaddition Involving Regitz Diazo Transfer.
Organic letters, 2016, 18, 6034-6037
1555908 CIFC16 H16 O SP 1 21 17.5678; 5.1454; 16.9271
90; 98.7561; 90		651.45Gómez, José Enrique; Guo, Wusheng; Kleij, Arjan W.
Palladium-Catalyzed Stereoselective Formation of Substituted Allylic Thioethers and Sulfones.
Organic letters, 2016, 18, 6042-6045
1555909 CIFC16 H16 O3 SP 1 21/n 17.9679; 11.4739; 14.9692
90; 93.356; 90		1366.18Gómez, José Enrique; Guo, Wusheng; Kleij, Arjan W.
Palladium-Catalyzed Stereoselective Formation of Substituted Allylic Thioethers and Sulfones.
Organic letters, 2016, 18, 6042-6045
1555910 CIFC40 H52 N2 Si2P -18.3992; 10.526; 11.746
68.85; 80.94; 76.25		937.8Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555911 CIFC32 H36 N2 Si2P 1 21/c 115.6326; 6.4203; 14.8783
90; 100.516; 90		1468.2Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555912 CIFC36 H40 N2 Si2P 1 21/c 16.5863; 32.7261; 7.6981
90; 112.553; 90		1532.39Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555913 CIFC34 H40 N2 Si2P 1 21/c 16.5947; 32.761; 7.661
90; 113.1; 90		1522.4Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555914 CIFC30 H28 N2P -16.0278; 11.373; 17.547
78.6; 83.43; 78.73		1152.9Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555915 CIFC36 H44 N2 Si2P -16.585; 7.8652; 17.0204
78.833; 83.504; 66.118		790.2Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555916 CIFC28 H28 N2 Si2P 1 21/c 16.247; 22.6384; 8.7822
90; 100.885; 90		1219.65Granger, Devin B.; Mei, Yaochuan; Thorley, Karl J.; Parkin, Sean R.; Jurchescu, Oana D.; Anthony, John E.
Synthesis and Electrical Properties of Derivatives of 1,4-bis(trialkylsilylethynyl)benzo[2,3-b:5,6-b']diindolizines.
Organic letters, 2016, 18, 6050-6053
1555917 CIFC19 H26 N2 OP b c a8.7863; 19.6959; 19.81
90; 90; 90		3428.2Peng, Jianwen; Gao, Yang; Hu, Weigao; Gao, Yinglan; Hu, Miao; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng
Palladium-Catalyzed Multicomponent Reaction (MCR) of Propargylic Carbonates with Isocyanides.
Organic letters, 2016, 18, 5924-5927
1555918 CIFC24 H34 Br N3 OP 1 21/c 17.0557; 18.3411; 18.3448
90; 93.837; 90		2368.67Peng, Jianwen; Gao, Yang; Hu, Weigao; Gao, Yinglan; Hu, Miao; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng
Palladium-Catalyzed Multicomponent Reaction (MCR) of Propargylic Carbonates with Isocyanides.
Organic letters, 2016, 18, 5924-5927
1555919 CIFC15 H12 N2 OP 656.1726; 6.1726; 54.71
90; 90; 120		1805.2Yuan, Bingxiang; Zhang, Fuming; Li, Zhuomei; Yang, Shenghua; Yan, Rulong
AgNO<sub>2</sub> as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines.
Organic letters, 2016, 18, 5928-5931
1555920 CIFC15 H12 N2 OP 656.1726; 6.1726; 54.71
90; 90; 120		1805.2Yuan, Bingxiang; Zhang, Fuming; Li, Zhuomei; Yang, Shenghua; Yan, Rulong
AgNO<sub>2</sub> as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines.
Organic letters, 2016, 18, 5928-5931
1555921 CIFC29 H28 O6P -18.652; 9.9706; 14.1796
78.8291; 89.706; 78.2333		1174.07Shirinian, Valerii Z.; Lvov, Andrey G.; Yadykov, Anton V.; Yaminova, Liana V.; Kachala, Vadim V.; Markosyan, Ashot I.
Triaryl-Substituted Divinyl Ketones Cyclization: Nazarov Reaction versus Friedel-Crafts Electrophilic Substitution.
Organic letters, 2016, 18, 6260-6263
1555922 CIFC10 H17 N O3P 1 21 15.7737; 7.9024; 11.5568
90; 100.734; 90		518.07Choi, Chulho; Nuhant, Philippe; Mousseau, James J.; Yang, Xiaojing; Gerstenberger, Brian S.; Williams, Jessica M.; Wright, Stephen W.
Synthesis of Chiral Azabicycles from Pyroglutaminols.
Organic letters, 2016, 18, 5748-5751
1555923 CIFC11 H12 N2 O2P 1 21 16.9214; 6.4235; 11.479
90; 105.437; 90		491.94Choi, Chulho; Nuhant, Philippe; Mousseau, James J.; Yang, Xiaojing; Gerstenberger, Brian S.; Williams, Jessica M.; Wright, Stephen W.
Synthesis of Chiral Azabicycles from Pyroglutaminols.
Organic letters, 2016, 18, 5748-5751
1555924 CIFC13 H15 N O2P 21 21 215.8422; 10.2343; 19.63
90; 90; 90		1173.69Choi, Chulho; Nuhant, Philippe; Mousseau, James J.; Yang, Xiaojing; Gerstenberger, Brian S.; Williams, Jessica M.; Wright, Stephen W.
Synthesis of Chiral Azabicycles from Pyroglutaminols.
Organic letters, 2016, 18, 5748-5751
1555925 CIFC27 H20 F O PP 1 2/c 111.104; 9.075; 27.414
90; 91.04; 90		2762Hu, Gaobo; Shan, Changkai; Chen, Weizhu; Xu, Pengxiang; Gao, Yuxing; Zhao, Yufen
Copper-Catalyzed Direct Coupling of Unprotected Propargylic Alcohols with P(O)H Compounds: Access to Allenylphosphoryl Compounds under Ligand- and Base-Free Conditions.
Organic letters, 2016, 18, 6066-6069
1555926 CIFC18 H17 N O3 SP 1 21/c 113.1754; 12.8893; 9.6352
90; 97.16; 90		1623.51Siva Kumari, A. Leela; Siva Reddy, Alla; Swamy, K. C. Kumara
Transition Metal-Free Cascade Cyclization of Epoxy-Ynamides: To Go for 1,3-Oxazines or 1,4-Oxazines?
Organic letters, 2016, 18, 5752-5755
1555927 CIFC22 H19 N O3 SP 1 21/c 119.1531; 7.3529; 13.812
90; 108.013; 90		1849.82Siva Kumari, A. Leela; Siva Reddy, Alla; Swamy, K. C. Kumara
Transition Metal-Free Cascade Cyclization of Epoxy-Ynamides: To Go for 1,3-Oxazines or 1,4-Oxazines?
Organic letters, 2016, 18, 5752-5755
1555928 CIFC26 H33 N4 O3 SP 1 21/c 15.8986; 26.6087; 16.7845
90; 96.428; 90		2617.8Siva Kumari, A. Leela; Siva Reddy, Alla; Swamy, K. C. Kumara
Transition Metal-Free Cascade Cyclization of Epoxy-Ynamides: To Go for 1,3-Oxazines or 1,4-Oxazines?
Organic letters, 2016, 18, 5752-5755
1555929 CIFC17 H16 N4 O3 SP c a b8.75; 15.7853; 24.961
90; 90; 90		3447.6Siva Kumari, A. Leela; Siva Reddy, Alla; Swamy, K. C. Kumara
Transition Metal-Free Cascade Cyclization of Epoxy-Ynamides: To Go for 1,3-Oxazines or 1,4-Oxazines?
Organic letters, 2016, 18, 5752-5755
1555930 CIFC26 H24 N4 O3 SP 1 21/c 18.3734; 25.188; 11.2668
90; 98.394; 90		2350.8Siva Kumari, A. Leela; Siva Reddy, Alla; Swamy, K. C. Kumara
Transition Metal-Free Cascade Cyclization of Epoxy-Ynamides: To Go for 1,3-Oxazines or 1,4-Oxazines?
Organic letters, 2016, 18, 5752-5755
1555931 CIFC19 H19 N O4P -19.0147; 9.2814; 10.9521
69.621; 79.392; 70.853		808.95Reddy, B. Narendraprasad; Ramana, Chepuri V.
Synthesis of Functionalized 6-Hydroxy-2-oxindole Derivatives by Phenoxide Cyclization.
Organic letters, 2016, 18, 6264-6267
1555932 CIFC15 H15 N O4P 1 21/c 16.8886; 12.9983; 14.7636
90; 94.523; 90		1317.8Reddy, B. Narendraprasad; Ramana, Chepuri V.
Synthesis of Functionalized 6-Hydroxy-2-oxindole Derivatives by Phenoxide Cyclization.
Organic letters, 2016, 18, 6264-6267
1555933 CIFC21 H21 N O5P 1 21/n 19.0841; 19.3749; 31.8706
90; 95.862; 90		5580Reddy, B. Narendraprasad; Ramana, Chepuri V.
Synthesis of Functionalized 6-Hydroxy-2-oxindole Derivatives by Phenoxide Cyclization.
Organic letters, 2016, 18, 6264-6267
1555934 CIFC24 H21 N O6P -17.3578; 12.184; 13.0111
86.19; 75.871; 74.332		1089.1Gao, Peng; Wang, Juan; Bai, Zi-Jing; Shen, Li; Yan, Yun-Yun; Yang, De-Suo; Fan, Ming-Jin; Guan, Zheng-Hui
Synthesis of Polycarbonyl Pyrroles via K<sub>2</sub>S<sub>2</sub>O<sub>8</sub>-Mediated Oxidative Cyclization of Enamines.
Organic letters, 2016, 18, 6074-6077
1555935 CIFC20 H17 N O4P 1 21/c 113.9835; 9.8343; 13.1233
90; 100.67; 90		1773.5Gao, Peng; Wang, Juan; Bai, Zi-Jing; Shen, Li; Yan, Yun-Yun; Yang, De-Suo; Fan, Ming-Jin; Guan, Zheng-Hui
Synthesis of Polycarbonyl Pyrroles via K<sub>2</sub>S<sub>2</sub>O<sub>8</sub>-Mediated Oxidative Cyclization of Enamines.
Organic letters, 2016, 18, 6074-6077
1555936 CIFC27 H35 N3 O6P 1 21 15.1132; 29.4098; 8.8232
90; 92.686; 90		1325.36Liew, Sean K.; Kaldas, Sherif J.; Yudin, Andrei K.
A Linchpin Synthesis of 6-Hydroxyceramides from Aziridine Aldehydes.
Organic letters, 2016, 18, 6268-6271
1555937 CIFC33 H28 Cl N O6P 21 21 218.8021; 9.9889; 32.4893
90; 90; 90		2856.6Xiao, Yu; Lin, Jun-Bing; Zhao, Yin-Na; Liu, Jin-Yu; Xu, Peng-Fei
Exploring the Reactivity of Nitro-Activated 1,3-Enynes in an Organocatalytic One-Pot, Three-Component Coupling Reaction: A Tandem Catalytic Approach to a Novel 3-Nitrochroman Scaffold.
Organic letters, 2016, 18, 6276-6279
1555938 CIFC29 H26 F N O2 SP 1 21 110.243; 9.991; 12.37
90; 106.182; 90		1215.76Xiao, Guolan; Ma, Chaoqun; Xing, Dong; Hu, Wenhao
Enantioselective Synthesis of α-Mercapto-β-amino Esters via Rh(II)/Chiral Phosphoric Acid-Cocatalyzed Three-Component Reaction of Diazo Compounds, Thiols, and Imines.
Organic letters, 2016, 18, 6086-6089
1555939 CIFC15 H16 O2P 1 21 19.2014; 10.8506; 12.1
90; 91.8595; 90		1207.44Nelson, Jr, Shawn D; Wawer, Mathias J.; Schreiber, Stuart L.
Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives.
Organic letters, 2016, 18, 6280-6283
1555940 CIFC15 H18 O4P 1 21 16.9162; 15.552; 12.5396
90; 102.049; 90		1319.05Nelson, Jr, Shawn D; Wawer, Mathias J.; Schreiber, Stuart L.
Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives.
Organic letters, 2016, 18, 6280-6283
1555941 CIFC15 H20 O2P 21 21 216.3597; 8.5694; 22.6596
90; 90; 90		1234.92Nelson, Jr, Shawn D; Wawer, Mathias J.; Schreiber, Stuart L.
Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives.
Organic letters, 2016, 18, 6280-6283
1555942 CIFC60.84 H63.33 I6 N14.07 Zn3C 1 2/c 136.538; 14.716; 30.585
90; 102.234; 90		16072Waldhart, Greyson W.; Mankad, Neal P.; Santarsiero, Bernard D.
Improvements to the Practical Usability of the "Crystalline Sponge" Method for Organic Structure Determination.
Organic letters, 2016, 18, 6112-6115
1555943 CIFC48.64 H34.53 I6 N14.11 O4.21 Zn3C 1 2/c 134.026; 15.046; 30.424
90; 100.625; 90		15308.7Waldhart, Greyson W.; Mankad, Neal P.; Santarsiero, Bernard D.
Improvements to the Practical Usability of the "Crystalline Sponge" Method for Organic Structure Determination.
Organic letters, 2016, 18, 6112-6115
1555944 CIFC20 H26 O5P 21 21 2116.4591; 7.2887; 14.371
90; 90; 90		1724Mahdjour, Soumicha; Harche-Kaid, Meriem; Haidour, Alí; Chahboun, Rachid; Alvarez-Manzaneda, Enrique
Short Route to Cassane-Type Diterpenoids: Synthesis of the Supposed Structure of Benthaminin 1.
Organic letters, 2016, 18, 5964-5967
1555945 CIFC16 H12 N2 O2C 1 2/c 123.889; 10.077; 12.378
90; 119.348; 90		2597.3Kong, Lingkai; Wang, Mengdan; Zhang, Fangfang; Xu, Murong; Li, Yanzhong
Copper-Catalyzed Oxidative Dearomatization/Spirocyclization of Indole-2-Carboxamides: Synthesis of 2-Spiro-pseudoindoxyls.
Organic letters, 2016, 18, 6124-6127
1555946 CIFC23 H39 O3P 1 21 17.46386; 20.34874; 14.16918
90; 92.7434; 90		2149.55Liu, Shao-Nan; Huang, Dane; Morris-Natschke, Susan L; Ma, Hang; Liu, Zhi-Hong; Seeram, Navindra P.; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii.
Organic letters, 2016, 18, 6132-6135
1555947 CIFC20 H32 O3P 21 21 217.4778; 9.96312; 24.19049
90; 90; 90		1802.24Liu, Shao-Nan; Huang, Dane; Morris-Natschke, Susan L; Ma, Hang; Liu, Zhi-Hong; Seeram, Navindra P.; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii.
Organic letters, 2016, 18, 6132-6135
1555948 CIFC26 H22 Cl N O4 SC 1 2/c 122.1581; 25.2375; 10.6695
90; 108.244; 90		5666.6Liu, Kang; Chang, Xin; Wang, Chun-Jiang
Nickel(II)-Catalyzed Cascade Vinylogous Mukaiyama 1,6-Michael/Michael Addition of 2-Silyloxyfuran with N-Sulfonyl-1-aza-1,3-dienes: Access to Fused Piperidine/Butyrolactone Skeletons.
Organic letters, 2016, 18, 6288-6291
1555949 CIFC14 H12 N2 OP 1 21/c 16.0068; 15.6019; 12.0874
90; 95.78; 90		1127Youn, So Won; Kim, Yi Hyun
Pd(II)/Ag(I)-Promoted One-Pot Synthesis of Cyclic Ureas from (Hetero)Aromatic Amines and Isocyanates.
Organic letters, 2016, 18, 6140-6143
1555950 CIFC24 H34 O4P 1 21 112.0052; 7.5696; 12.6467
90; 113.646; 90		1052.77Michalak, Karol; Morawiak, Maja; Wicha, Jerzy
Synthetic Approach to the Core Structure of Oleandrin and Related Cardiac Glycosides with Highly Functionalized Ring D.
Organic letters, 2016, 18, 6148-6151
1555951 CIFC26 H38 O5P 1 21 16.1334; 25.169; 7.7489
90; 95.807; 90		1190.1Michalak, Karol; Morawiak, Maja; Wicha, Jerzy
Synthetic Approach to the Core Structure of Oleandrin and Related Cardiac Glycosides with Highly Functionalized Ring D.
Organic letters, 2016, 18, 6148-6151
1555952 CIFC14 H16 Cl4 O4P 41 21 29.2923; 9.2923; 38.5
90; 90; 90		3324.4Sarkar, Rahul; Mukherjee, Santanu
Catalytic Enantioselective Desymmetrization of Norbornenoquinones via C(sp<sup>2</sup>)-H Alkylation.
Organic letters, 2016, 18, 6160-6163
1555953 CIFC30 H27 N3 O3C 1 c 114.279; 20.305; 9.8589
90; 119.294; 90		2492.9Zhao, Yu; Chen, Jia-Rong; Xiao, Wen-Jing
Synthesis of Hydrazide-Containing Chroman-2-ones and Dihydroquinolin-2-ones via Photocatalytic Radical Cascade Reaction of Aroylhydrozones.
Organic letters, 2016, 18, 6304-6307
1555954 CIFC13 H13 N OP 1 21/n 113.4161; 5.5776; 15.6055
90; 106.023; 90		1122.39Cheng, Wanli; Tang, Yanhua; Xu, Ze-Feng; Li, Chuan-Ying
Synthesis of Multifunctionalized 2-Carbonylpyrrole by Rhodium-Catalyzed Transannulation of 1-Sulfonyl-1,2,3-triazole with β-Diketone.
Organic letters, 2016, 18, 6168-6171
1555955 CIFC13 H15 Cl OP 21 21 218.7518; 8.9722; 13.5378
90; 90; 90		1063.03Han, Yixin; Breitler, Simon; Zheng, Shao-Liang; Corey, E. J.
Enantioselective Conversion of Achiral Cyclohexadienones to Chiral Cyclohexenones by Desymmetrization.
Organic letters, 2016, 18, 6172-6175
1555956 CIFC21 H16 OP b a 218.9446; 24.3426; 6.2244
90; 90; 90		2870.45Yoon, Hyung; Lossouarn, Alexis; Landau, Felicitas; Lautens, Mark
Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne Insertion.
Organic letters, 2016, 18, 6324-6327
1555957 CIFC22 H17 N OP 1 21/c 111.8751; 8.3673; 15.6764
90; 90.689; 90		1557.5Yoon, Hyung; Lossouarn, Alexis; Landau, Felicitas; Lautens, Mark
Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne Insertion.
Organic letters, 2016, 18, 6324-6327
1555958 CIFC53 H44 Cl3 N O P2 PdP 1 21/c 111.7599; 18.0933; 23.3373
90; 103.385; 90		4830.7Yoon, Hyung; Lossouarn, Alexis; Landau, Felicitas; Lautens, Mark
Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne Insertion.
Organic letters, 2016, 18, 6324-6327
1555959 CIFC26 H18 Cl N OP -18.9082; 9.9372; 11.1764
90.17; 100.71; 95.382		967.63Samineni, Ramesh; Bandi, Chandramohan Reddy C.; Srihari, Pabbaraja; Mehta, Goverdhan
Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones.
Organic letters, 2016, 18, 6184-6187
1555960 CIFC21 H21 N3 O2P 1 21 18.51; 12.408; 8.644
90; 90.049; 90		912.7Samineni, Ramesh; Bandi, Chandramohan Reddy C.; Srihari, Pabbaraja; Mehta, Goverdhan
Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones.
Organic letters, 2016, 18, 6184-6187
1555961 CIFC26 H18 Br N OP -18.996; 9.168; 14.637
90.061; 106.475; 117.452		1014.9Samineni, Ramesh; Bandi, Chandramohan Reddy C.; Srihari, Pabbaraja; Mehta, Goverdhan
Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones.
Organic letters, 2016, 18, 6184-6187
1555962 CIFC57 H52 Cl4 N2 O7P 1 21/n 111.5586; 37.6596; 12.2407
90; 110.032; 90		5005.9Zhu, Congzhi; Mu, Anthony U.; Lin, Yen-Hao; Guo, Zi-Hao; Yuan, Tianyu; Wheeler, Steven E.; Fang, Lei
Molecular Coplanarity and Self-Assembly Promoted by Intramolecular Hydrogen Bonds.
Organic letters, 2016, 18, 6332-6335
1555963 CIFC66 H5 Co OP n a 2119.3264; 16.2685; 9.8756
90; 90; 90		3105Hashikawa, Yoshifumi; Murata, Michihisa; Wakamiya, Atsushi; Murata, Yasujiro
Co(I)-Mediated Removal of Addends on the C<sub>60</sub> Cage and Formation of the Monovalent Cobalt Complex CpCo(CO)(η<sup>2</sup>-C<sub>60</sub>).
Organic letters, 2016, 18, 6348-6351
1555964 CIFC27 H27 N3P -110.8707; 12.3272; 16.2931
79.118; 82.74; 72.757		2041.96Fandrick, Daniel R.; Hart, Christine A.; Okafor, Ifeanyi S.; Mercadante, Michael A.; Sanyal, Sanjit; Masters, James T.; Sarvestani, Max; Fandrick, Keith R.; Stockdill, Jennifer L.; Grinberg, Nelu; Gonnella, Nina; Lee, Heewon; Senanayake, Chris H.
Copper-Catalyzed Asymmetric Propargylation of Cyclic Aldimines.
Organic letters, 2016, 18, 6192-6195
1555965 CIFC19 H18 OP 21 21 215.9076; 8.2748; 28.655
90; 90; 90		1400.8Kusy, Rafał; Grela, Karol
E- and Z-Selective Transfer Semihydrogenation of Alkynes Catalyzed by Standard Ruthenium Olefin Metathesis Catalysts.
Organic letters, 2016, 18, 6196-6199
1555966 CIFC27 H22 Cl N O5 SP 1 21/c 110.9967; 16.5944; 25.1871
90; 91.593; 90		4594.46Xuan, Jun; Daniliuc, Constantin G.; Studer, Armido
Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis.
Organic letters, 2016, 18, 6372-6375
1555967 CIFC21 H22 F2 N2 O7C 1 2 113.014; 9.45; 18.211
90; 98.828; 90		2213.1Evans, Christopher E.; Matarlo, Joe S.; Tonge, Peter J.; Tan, Derek S.
Stereoselective Synthesis, Docking, and Biological Evaluation of Difluoroindanediol-Based MenE Inhibitors as Antibiotics.
Organic letters, 2016, 18, 6384-6387
1555968 CIFC24 H16 N2 O2P -17.1492; 10.4607; 12.1607
77.086; 77.386; 87.983		864.96Zhang, Cheng; Huang, Jingjing; Qiu, Lihua; Xu, Xinfang
Thermally Induced [3 + 2] Cycloaddition of Alkynyl-Tethered Diazoamides: Synthetic and Mechanistic Insights.
Organic letters, 2016, 18, 6208-6211
1555969 CIFC12 H21 N3 O3P 1 21/c 112.2885; 6.3383; 17.583
90; 100.49; 90		1346.62Zhang, Cheng; Huang, Jingjing; Qiu, Lihua; Xu, Xinfang
Thermally Induced [3 + 2] Cycloaddition of Alkynyl-Tethered Diazoamides: Synthetic and Mechanistic Insights.
Organic letters, 2016, 18, 6208-6211
1555970 CIFC23 H31 NP 21 21 217.1278; 11.0317; 24.0691
90; 90; 90		1892.6Dethe, Dattatraya H.; Sau, Susanta Kumar; Mahapatra, Samarpita
Biomimetic Enantioselective Total Synthesis of (-)-Mycoleptodiscin A.
Organic letters, 2016, 18, 6392-6395
1555971 CIFC33 H21 N O SP 1 21/c 122.035; 10.8485; 22.733
90; 114.59; 90		4941.4Shankar, Majji; Ghosh, Koushik; Mukherjee, Kallol; Rit, Raja K.; Sahoo, Akhila K.
Ru-Catalyzed One-Pot Diannulation of Heteroaryls: Direct Access to π-Conjugated Polycyclic Amides.
Organic letters, 2016, 18, 6416-6419
1555972 CIFC35 H22 F N OP 1 21/c 117.6372; 11.5066; 12.8191
90; 107.487; 90		2481.3Shankar, Majji; Ghosh, Koushik; Mukherjee, Kallol; Rit, Raja K.; Sahoo, Akhila K.
Ru-Catalyzed One-Pot Diannulation of Heteroaryls: Direct Access to π-Conjugated Polycyclic Amides.
Organic letters, 2016, 18, 6416-6419
1555973 CIFC19 H29 B O4P 1 21/c 110.8565; 16.1793; 12.2433
90; 114.148; 90		1962.3Butcher, Trevor W.; McClain, Edward J.; Hamilton, Tyler G.; Perrone, Trina M.; Kroner, Kayla M.; Donohoe, Gregory C.; Akhmedov, Novruz G.; Petersen, Jeffrey L.; Popp, Brian V.
Regioselective Copper-Catalyzed Boracarboxylation of Vinyl Arenes.
Organic letters, 2016, 18, 6428-6431
1555974 CIFC17 H14 Br N3 OP 1 21 15.4346; 9.6489; 14.5339
90; 99.157; 90		752.41Vyas, Vijyesh K.; Bhanage, Bhalchandra M.
Kinetic Resolution Driven Diastereo- and Enantioselective Synthesis of cis-β-Heteroaryl Amino Cycloalkanols by Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation.
Organic letters, 2016, 18, 6436-6439
1555975 CIFC22 H18 F N O3P -16.2872; 10.7075; 13.7223
80.562; 85.731; 87.096		908.06Liu, Jianchao; Peng, Hui; Lu, Lin; Xu, Xiaobing; Jiang, Huanfeng; Yin, Biaolin
Diastereospecific and Enantioselective Access to Dispirooxindoles from Furfurylcyclobutanols by Means of a Pd-Catalyzed Arylative Dearomatization/Ring Expansion Cascade.
Organic letters, 2016, 18, 6440-6443
1555976 CIFC26 H16 Cl2P 1 21/c 111.7842; 10.5042; 16.7068
90; 109.462; 90		1949.87Li, Jen-Yi; Chang, Hung-Ing; Feng, Chieh-Ning; Wu, Yao-Ting
Rotation of Aryl Groups in 9,10-Diarylphenanthrenes: Does the Rotational Barrier Become Lower as the Backbone Becomes More Crowded?
Organic letters, 2016, 18, 6444-6447
1555977 CIFC34 H34P 21 21 217.2192; 12.2678; 27.633
90; 90; 90		2447.3Li, Jen-Yi; Chang, Hung-Ing; Feng, Chieh-Ning; Wu, Yao-Ting
Rotation of Aryl Groups in 9,10-Diarylphenanthrenes: Does the Rotational Barrier Become Lower as the Backbone Becomes More Crowded?
Organic letters, 2016, 18, 6444-6447
1555978 CIFC26 H16 Cl2P 1 21/c 19.1927; 29.468; 7.4968
90; 104.857; 90		1962.9Li, Jen-Yi; Chang, Hung-Ing; Feng, Chieh-Ning; Wu, Yao-Ting
Rotation of Aryl Groups in 9,10-Diarylphenanthrenes: Does the Rotational Barrier Become Lower as the Backbone Becomes More Crowded?
Organic letters, 2016, 18, 6444-6447
1555979 CIFC34 H34P 1 21/n 110.724; 14.6596; 15.9412
90; 106.043; 90		2408.5Li, Jen-Yi; Chang, Hung-Ing; Feng, Chieh-Ning; Wu, Yao-Ting
Rotation of Aryl Groups in 9,10-Diarylphenanthrenes: Does the Rotational Barrier Become Lower as the Backbone Becomes More Crowded?
Organic letters, 2016, 18, 6444-6447
1555980 CIFC26 H27 N7 O2P 1 21 111.8603; 9.4892; 12.0188
90; 118.477; 90		1188.99Shiomi, Noriyuki; Yamamoto, Keisuke; Nagasaki, Kazuma; Hatanaka, Tsubasa; Funahashi, Yasuhiro; Nakamura, Shuichi
Enantioselective Oxidative Ring-Opening Reaction of Aziridines with α-Nitroesters Using Cinchona Alkaloid Amide/Nickel(II) Catalysts.
Organic letters, 2017, 19, 74-77
1555981 CIFC22 H19 Br O2P 1 21 111.8971; 5.9845; 12.3079
90; 95.961; 90		871.56Ming, Jialin; Hayashi, Tamio
Aryloxymethyltrifluoroborates for Rhodium-Catalyzed Asymmetric Conjugate Arylation. o-Methoxyarylation through 1,4-Rhodium Shift.
Organic letters, 2016, 18, 6452-6455
1555982 CIFC22 H22 N2 O2P b c a15.792; 12.08; 19.334
90; 90; 90		3688.3Hu, Ming; Zou, Hua-Xu; Song, Ren-Jie; Xiang, Jian-Nan; Li, Jin-Heng
Copper-Catalyzed C-H Oxidative Radical Functionalization and Annulation of Aniline-Linked 1,7-Enynes: Evidence for a 1,5-Hydride Shift Mechanism.
Organic letters, 2016, 18, 6460-6463
1555983 CIFC13 H14 O3P 1 21/c 18.02; 19.607; 7.492
90; 95.022; 90		1173.6Sun, Peng; Gao, Shang; Yang, Chi; Guo, Songjin; Lin, Aijun; Yao, Hequan
Controllable Rh(III)-Catalyzed Annulation between Salicylaldehydes and Diazo Compounds: Divergent Synthesis of Chromones and Benzofurans.
Organic letters, 2016, 18, 6464-6467
1555984 CIFC28 H24 Br N O2P 21 21 2110.8033; 12.0109; 17.2824
90; 90; 90		2242.52Shi, Ming-Lin; Zhan, Gu; Zhou, Su-Lan; Du, Wei; Chen, Ying-Chun
Asymmetric Inverse-Electron-Demand Oxa-Diels-Alder Reaction of Allylic Ketones through Dienamine Catalysis.
Organic letters, 2016, 18, 6480-6483
1555985 CIFC22 H28 O8P 21 21 217.8152; 12.0816; 21.667
90; 90; 90		2045.8Wu, Xing-De; Luo, Dan; Tu, Wen-Chao; Deng, Zhen-Tao; Chen, Xue-Jiao; Su, Jia; Ji, Xu; Zhao, Qin-Shi
Hypophyllins A-D, Labdane-Type Diterpenoids with Vasorelaxant Activity from Hypoestes phyllostachya "Rosea".
Organic letters, 2016, 18, 6484-6487
1555986 CIFC21 H28 O6P 21 21 219.478; 9.5117; 21.743
90; 90; 90		1960.2Wu, Xing-De; Luo, Dan; Tu, Wen-Chao; Deng, Zhen-Tao; Chen, Xue-Jiao; Su, Jia; Ji, Xu; Zhao, Qin-Shi
Hypophyllins A-D, Labdane-Type Diterpenoids with Vasorelaxant Activity from Hypoestes phyllostachya "Rosea".
Organic letters, 2016, 18, 6484-6487
1555987 CIFC21 H30 O6P 21 21 216.62; 10.9943; 27.0538
90; 90; 90		1969Wu, Xing-De; Luo, Dan; Tu, Wen-Chao; Deng, Zhen-Tao; Chen, Xue-Jiao; Su, Jia; Ji, Xu; Zhao, Qin-Shi
Hypophyllins A-D, Labdane-Type Diterpenoids with Vasorelaxant Activity from Hypoestes phyllostachya "Rosea".
Organic letters, 2016, 18, 6484-6487
1555988 CIFC21 H28 O6P 1 21 17.128; 13.9482; 9.3993
90; 92.464; 90		933.64Wu, Xing-De; Luo, Dan; Tu, Wen-Chao; Deng, Zhen-Tao; Chen, Xue-Jiao; Su, Jia; Ji, Xu; Zhao, Qin-Shi
Hypophyllins A-D, Labdane-Type Diterpenoids with Vasorelaxant Activity from Hypoestes phyllostachya "Rosea".
Organic letters, 2016, 18, 6484-6487
1555989 CIFC18 H21 N O2P 1 21/n 112.2561; 15.5951; 16.3454
90; 97.262; 90		3099.12Johnson, Thomas; Pultar, Felix; Menke, Friedericke; Lautens, Mark
Palladium-Catalyzed α-Arylation of Vinylogous Esters for the Synthesis of γ,γ-Disubstituted Cyclohexenones.
Organic letters, 2016, 18, 6488-6491
1555990 CIFC47 H50 N2 O5 S SiC 1 2/c 116.0823; 18.0956; 28.619
90; 97.4057; 90		8259.2Andreansky, Eric S.; Blakey, Simon B.
An Iminium Ion Cascade Annulation Strategy for the Synthesis of Akuammiline Alkaloid Pentacyclic Core Structures.
Organic letters, 2016, 18, 6492-6495
1555991 CIFC31 H18 O8P 1 21/c 117.4605; 8.5215; 15.4752
90; 103.931; 90		2234.82Zhang, Ai Hua; Liu, Wen; Jiang, Nan; Xu, Qiang; Tan, Ren Xiang
Spirodalesol, an NLRP3 Inflammasome Activation Inhibitor.
Organic letters, 2016, 18, 6496-6499
1555992 CIFC26 H24 N2 O2P -18.1158; 9.2869; 14.1457
86.852; 84.763; 70.523		1000.62Fan, Ling; Liu, Meilin; Ye, Yu; Yin, Guodong
Synthesis of 6-Substituted 6H-Indolo[2,3-b]quinolines from Isoindigos.
Organic letters, 2017, 19, 186-189
1555993 CIFC21 H13 F N2P 4311.1632; 11.1632; 12.0079
90; 90; 90		1496.4Fan, Ling; Liu, Meilin; Ye, Yu; Yin, Guodong
Synthesis of 6-Substituted 6H-Indolo[2,3-b]quinolines from Isoindigos.
Organic letters, 2017, 19, 186-189
1555994 CIFC19 H27 Br N O2 SiP 21 21 2110.5667; 11.1762; 18.221
90; 90; 90		2151.8Alicea-Matías, Eyleen; Soderquist, John A.
Asymmetric Propargylboration of Aldimines and Ketimines with the Borabicyclo[3.3.2]decanes: Novel Entries to Allenyl Carbinamines, Amino Acids, and Their α-Methyl Counterparts.
Organic letters, 2017, 19, 336-339
1555995 CIFC36 H27 N O2 SR -3 :H37.5582; 37.5582; 9.9323
90; 90; 120		12133.6Jalal, Swapnadeep; Paul, Kartick; Jana, Umasish
Iron-Catalyzed 1,5-Enyne Cycloisomerization via 5-Endo-Dig Cyclization for the Synthesis of 3-(Inden-1-yl)indole Derivatives.
Organic letters, 2016, 18, 6512-6515
1555996 CIFC21 H22 Br N O2P 1 21 16.0625; 19.5089; 16.3468
90; 96.885; 90		1919.44Wu, Chun-Yan; Yu, Yue-Na; Xu, Ming-Hua
Construction of Chiral Tricyclic Indoles through a Rhodium-Catalyzed Asymmetric Arylation Protocol.
Organic letters, 2017, 19, 384-387
1555997 CIFC21 H15 N3 O2P -17.1592; 9.8482; 12.3493
81.6372; 83.2218; 80.227		845.03Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin
Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones.
Organic letters, 2017, 19, 516-519
1555998 CIFC20 H12 F3 N3P 1 21/c 111.696; 9.0705; 15.811
90; 102.782; 90		1635.8Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin
Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones.
Organic letters, 2017, 19, 516-519
1555999 CIFC17 H17 N O3P -18.4056; 9.8583; 10.2022
69.4122; 78.7895; 71.4852		747.18Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin
Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones.
Organic letters, 2017, 19, 516-519
1556000 CIFC19 H24 N2 O2 SP 1 21 111.0611; 6.743; 13.0444
90; 102.392; 90		950.25Ma, Peng-Ju; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diastereoselective Electrophilic α-Hydroxyamination of N-tert-Butanesulfinyl Imidates.
Organic letters, 2017, 19, 670-673
1556001 CIFC30 H30 N2 O3R -3 :H26.495; 26.495; 25.84
90; 90; 120		15709Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556002 CIFC29 H28 N2 O3P 1 21/c 112.7136; 19.6481; 10.0368
90; 104.806; 90		2423.9Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556003 CIFC29 H28 N2 O3P 1 21/c 18.088; 29.039; 10.3957
90; 98.253; 90		2416.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556004 CIFC28 H26 N2 O3P -19.715; 11.622; 13.28
64.317; 86.248; 74.246		1298.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556005 CIFC26 H30 N2 O3P 1 21/c 111.5919; 14.5845; 13.8674
90; 97.872; 90		2322.4Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556006 CIFC34 H36 Cl2 N2 O5P 1 21/c 110.3241; 23.365; 13.7004
90; 99.642; 90		3258.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556007 CIFC33 H34 N2 O5P 1 21/c 113.9135; 11.8443; 18.4125
90; 108.518; 90		2877.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556008 CIFC29.5 H29 Cl N2 O3 SP 32 2 118.4813; 18.4813; 16.4257
90; 90; 120		4858.7Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556009 CIFC26 H30 N2 O3P 1 21/n 19.5688; 10.3956; 23.8948
90; 96.847; 90		2359.9Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556010 CIFC24 H24 N2 O2P 1 21/c 110.9969; 11.8906; 15.8497
90; 106.796; 90		1984.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556011 CIFC33 H34 N2 O5P 1 21/c 116.2583; 8.9359; 19.545
90; 95.231; 90		2827.7Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556012 CIFC26 H30 N2 O3P 1 21/c 115.2433; 10.1136; 14.943
90; 94.937; 90		2295.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556013 CIFC29 H28 N2 O3P 1 21/c 17.8226; 30.639; 10.1141
90; 98.682; 90		2396.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556014 CIFC29 H28 N2 O3 SP 1 21/c 18.6571; 29.45; 10.2183
90; 98.7924; 90		2574.56Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556015 CIFC26 H30 N2 O3C 1 2/c 117.3068; 12.0144; 22.5999
90; 96.044; 90		4673.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556016 CIFC29 H28 N2 O3C 1 2 122.49; 5.1816; 20.19
90; 90.78; 90		2352.6Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556017 CIFC29 H28 N2 O3 SP 1 21/n 119.7344; 12.7882; 20.279
90; 97.031; 90		5079.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556018 CIFC23 H17 Cl O3C 1 2 120.5553; 9.5675; 22.2196
90; 115.687; 90		3937.9Infante, Rebeca; Martin-Alvarez, Jose M; Andrés, Celia; Nieto, Javier
Dimethylzinc-Mediated Addition of Phenylacetylene to α-Diketones Catalyzed by Chiral Perhydro-1,3-benzoxazines.
Organic letters, 2017, 19, 1516-1519
1556019 CIFC16 H11 F N2 OP 21 21 218.4334; 9.1934; 16.9142
90; 90; 90		1311.4Jin, Yushu; Chen, Ming; Ge, Shaozhong; Hartwig, John F.
Palladium-Catalyzed, Enantioselective α-Arylation of α-Fluorooxindoles.
Organic letters, 2017, 19, 1390-1393
1556020 CIFC15 H12 N2 OP 1 21/n 116.4017; 7.1335; 20.0858
90; 95.665; 90		2338.6Yin, Kun; Zhang, Ronghua
Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature.
Organic letters, 2017, 19, 1530-1533
1556021 CIFC16 H14 N2 OP n a 219.9288; 26.7988; 4.7384
90; 90; 90		1260.79Yin, Kun; Zhang, Ronghua
Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature.
Organic letters, 2017, 19, 1530-1533
1556022 CIFC17 H13 N OP 1 21/c 14.0198; 13.908; 23.21
90; 94.2; 90		1294.1Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin
I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines.
Organic letters, 2017, 19, 1550-1553
1556023 CIFC11 H13 N S2P 1 21 19.9321; 22.705; 19.824
90; 98.538; 90		4420.9Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin
I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines.
Organic letters, 2017, 19, 1550-1553
1556024 CIFC43 H30 N2 O2P -110.4789; 12.074; 12.5011
92.552; 94.697; 98.319		1557.2Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling
Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions.
Organic letters, 2017, 19, 1658-1661
1556025 CIFC42 H28 N2 O2P b c a18.5446; 17.7946; 18.9442
90; 90; 90		6251.5Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling
Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions.
Organic letters, 2017, 19, 1658-1661
1556026 CIFC47 H36 Cl2 N4 O S ZnP -111.0032; 12.6313; 14.724
98.868; 96.16; 102.84		1950Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak
Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality.
Organic letters, 2017, 19, 1722-1725
1556027 CIFC51 H37 N5 O S ZnP 110.6689; 10.8762; 18.2817
83.457; 84.152; 77.519		2051.2Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak
Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality.
Organic letters, 2017, 19, 1722-1725
1556028 CIFC32 H27 Br O2P 1 21 19.624; 31.096; 13.229
90; 91.141; 90		3958Perveen, Saima; Zhao, Zhifei; Zhang, Guoxiang; Liu, Jian; Anwar, Muhammad; Fang, Xinqiang
Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis.
Organic letters, 2017, 19, 2470-2473
1556029 CIFC94 H64 O2P -19.9734; 11.3386; 15.3837
79.9686; 85.4756; 79.5603		1682.69Vadehra, Geeta S.; Jiang, Xing; Dotson, Jordan J.; Chu, Gong M.; Garcia-Garibay, Miguel A
High-Yielding and Divergent Paradigm for the Synthesis of D<sub>2h</sub>-Symmetric Octakis-Substituted Pentiptycenequinones.
Organic letters, 2017, 19, 1838-1841
1556030 CIFC24 H26 N2 O6P 1 21 111.0167; 8.4713; 13.145
90; 112.969; 90		1129.5Ran, Guang-Yao; Gong, Ming; Yue, Jing-Fei; Yang, Xing-Xing; Zhou, Su-Lan; Du, Wei; Chen, Ying-Chun
Asymmetric Cascade Assembly of 1,2-Diaza-1,3-dienes and α,β-Unsaturated Aldehydes via Dienamine Activation.
Organic letters, 2017, 19, 1874-1877
1556031 CIFC14 H9 N O3 SP 1 21/c 112.0277; 13.0209; 8.1447
90; 106.121; 90		1225.4Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556032 CIFC14 H13 N O3 SP 21 21 217.4865; 10.7242; 32.3467
90; 90; 90		2597.01Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556033 CIFC14 H12 N O3 SP 21 21 219.4952; 13.78766; 23.3234
90; 90; 90		3053.42Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556034 CIFC24 H24 N2 O3 SeP 1 21/c 19.4838; 10.5004; 21.1264
90; 90.868; 90		2103.6Foley, Christopher; Shaw, Arthur; Hulme, Christopher
Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles.
Organic letters, 2017, 19, 2238-2241
1556035 CIFC14 H16 N4 OP 1 21/m 17.7378; 6.7075; 12.6395
90; 102.323; 90		640.89Foley, Christopher; Shaw, Arthur; Hulme, Christopher
Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles.
Organic letters, 2017, 19, 2238-2241
1556036 CIFC28 H44 Cl2 N8 Ni O2I m -3 m17.0714; 17.0714; 17.0714
90; 90; 90		4975.2Zhang, Xingjie; Xia, Aiyou; Chen, Haoyi; Liu, Yuanhong
General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)<sub>2</sub>: Key Roles of DMAP.
Organic letters, 2017, 19, 2118-2121
1556037 CIFC23 H18 O2P 1 21 16.0965; 7.8294; 17.9271
90; 96.951; 90		849.41Zhang, Jingfang; Tang, Yuhai; Wei, Wen; Wu, Yong; Li, Yang; Zhang, Junjie; Zheng, Yuansuo; Xu, Silong
Organocatalytic Cloke-Wilson Rearrangement: DABCO-Catalyzed Ring Expansion of Cyclopropyl Ketones to 2,3-Dihydrofurans.
Organic letters, 2017, 19, 3043-3046
1556038 CIFC26 H34 O4 SiP 21 21 219.47; 15.075; 17.824
90; 90; 90		2544.6Han, Man-Yi; Xie, Xiaoyu; Zhou, Di; Li, Pinhua; Wang, Lei
Organocatalyzed Direct Aldol Reaction of Silyl Glyoxylates for the Synthesis of α-Hydroxysilanes.
Organic letters, 2017, 19, 2282-2285
1556039 CIFC16 H13 Br F3 N O3P 21 21 215.8132; 8.851; 31.166
90; 90; 90		1603.6Wang, Pei; Li, Hong-Feng; Zhao, Jia-Zhen; Du, Zhi-Hong; Da, Chao-Shan
Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones.
Organic letters, 2017, 19, 2634-2637
1556040 CIFC22 H26 O4 SP b c a5.5413; 15.8031; 45.3572
90; 90; 90		3971.92Zhurakovskyi, Oleksandr; Ellis, Sam R.; Thompson, Amber L.; Robertson, Jeremy
Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland-Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl.
Organic letters, 2017, 19, 2174-2177
1556041 CIFC19 H37 Br Cu N3 P2I 41 c d31.5316; 31.5316; 18.8701
90; 90; 90		18761.4Mastalir, Matthias; Pittenauer, Ernst; Stöger, Berthold; Allmaier, Günter; Kirchner, Karl
Three Different Reactions, One Catalyst: A Cu(I) PNP Pincer Complex as Catalyst for C-C and C-N Cross-Couplings.
Organic letters, 2017, 19, 2178-2181
1556042 CIFC27 H22 O SP 21 21 215.3756; 8.23448; 44.3104
90; 90; 90		1961.41Wang, Zhaobin; Sun, Jianwei
Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes.
Organic letters, 2017, 19, 2334-2337
1556043 CIFC11 H10 F7 N3 O2P 1 21/c 116.1302; 7.5328; 12.1195
90; 90.161; 90		1472.6Wang, Rui; Guan, Wei; Han, Zheng-Bo; Liang, Fushun; Suga, Takeo; Bi, Xihe; Nishide, Hiroyuki
Ambient-Light-Promoted Three-Component Annulation: Synthesis of Perfluoroalkylated Pyrimidines.
Organic letters, 2017, 19, 2358-2361
1556044 CIFC25 H31 N O7 SiP -19.5604; 11.3393; 12.5938
64.094; 79.058; 86.136		1205.56Parsons, Philip J.; Jones, Daniel R.; Walsh, Lee J.; Allen, Lewis A. T.; Onwubiko, Ada; Preece, Lewis; Board, Johnathan; White, Andrew J. P.
An Approach to the Core of Lactonamycin.
Organic letters, 2017, 19, 2533-2535
1556045 CIFC19 H20 O3C 1 2 117.9303; 6.8625; 13.4226
90; 99.456; 90		1629.16Iwamoto, Hiroaki; Akiyama, Sota; Hayama, Keiichi; Ito, Hajime
Copper(I)-Catalyzed Stereo- and Chemoselective Borylative Radical Cyclization of Alkyl Halides Bearing an Alkene Moiety.
Organic letters, 2017, 19, 2614-2617
1556046 CIFC12 H6 O S2P b c a5.541; 15.387; 22.574
90; 90; 90		1925Mitsudo, Koichi; Kurimoto, Yuji; Mandai, Hiroki; Suga, Seiji
Synthesis of 3-Benzo[b]thienyl 3-Thienyl Ether via an Addition-Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its π-Extended Derivatives.
Organic letters, 2017, 19, 2821-2824
1556047 CIFC19 H26 Cl N2 O RhP b c a8.0471; 16.3426; 29.6614
90; 90; 90		3900.8Long, Zhen; Yang, Yudong; You, Jingsong
Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles.
Organic letters, 2017, 19, 2781-2784
1556048 CIFC22 H24 Cl N2 O RhP 1 21/n 17.58618; 16.9757; 15.6843
90; 93.0656; 90		2016.94Long, Zhen; Yang, Yudong; You, Jingsong
Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles.
Organic letters, 2017, 19, 2781-2784
1556049 CIFC116 H112 Cl2 N10 NiP -112.6554; 19.7134; 21.0374
72.334; 80.809; 82.734		4919.7Yin, Bangshao; Kim, Taeyeon; Zhou, Mingbo; Huang, Weiming; Kim, Dongho; Song, Jianxin
Porphyrin-Azobenzene-Bodipy Triads: Syntheses, Structures, and Photophysical Properties.
Organic letters, 2017, 19, 2654-2657
1556050 CIFC27 H23 N O3 SP 21 21 2111.4379; 12.8956; 15.0848
90; 90; 90		2225Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin
Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations.
Organic letters, 2017, 19, 3111-3114
1556051 CIFC33 H26 Cl N O4 SP 21 21 218.9355; 14.869; 20.8047
90; 90; 90		2764.2Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin
Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations.
Organic letters, 2017, 19, 3111-3114
1556052 CIFC204 H280 N24 O20 S12P 1 21/n 122.6919; 27.504; 32.801
90; 93.8825; 90		20425Cholewiak, Agnieszka; Tycz, Agnieszka; Jurczak, Janusz
8-Propyldithieno[3,2-b:2',3'-e]pyridine-3,5-diamine (DITIPIRAM) Derivatives as Neutral Receptors Tailored for Binding of Carboxylates.
Organic letters, 2017, 19, 3001-3004
1556053 CIFC22 H22 Cl N O6C 1 2 121.5482; 6.1634; 16.9021
90; 111.981; 90		2081.59Drelich, Piotr; Moczulski, Marek; Albrecht, Łukasz
d<sup>0</sup>a<sup>3</sup> Synthon Equivalents for the Stereocontrolled Synthesis of Functionalized 1,4-Amino Alcohol Precursors.
Organic letters, 2017, 19, 3143-3146
1556054 CIFC19 H18 N2 O2 SP 1 21/n 17.8427; 22.614; 18.528
90; 93.229; 90		3280.8Wang, Xingyong; Liu, Chulong; Zeng, Xiaobao; Wang, Xuesong; Wang, Xinyan; Hu, Yuefei
Ruthenium-Catalyzed Synthesis of Fused Tricyclic 1H-2,3-Dihydropyrimido[1,2-a]quinolines in One Step.
Organic letters, 2017, 19, 3378-3381
1556055 CIFC19 H19 Cl N6 OC 1 2 120.4899; 9.7314; 10.0601
90; 101.493; 90		1965.72Li, Dan; Wang, Kezhou; Wang, Linqing; Wang, Yuan; Wang, Pengxin; Liu, Xin; Yang, Dongxu; Wang, Rui
Magnesium Catalysis Mediated Tetrazoles in Desymmetrization Reaction of Aziridines.
Organic letters, 2017, 19, 3211-3214
1556056 CIFC17.5 H14 N2 O1.5P 21 21 217.1969; 9.884; 38.6328
90; 90; 90		2748.11Mei, Guang-Jian; Bian, Chen-Yu; Li, Guo-Hao; Xu, Shao-Li; Zheng, Wen-Qin; Shi, Feng
Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization.
Organic letters, 2017, 19, 3219-3222
1556057 CIFC14 H10 N2 O2P b c a8.0739; 10.2485; 27.568
90; 90; 90		2281.1Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O.
Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers.
Organic letters, 2017, 19, 3512-3515
1556058 CIFC18 H18 N2 O3C 1 2/c 134.507; 7.3494; 13.4613
90; 110.662; 90		3194.3Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O.
Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers.
Organic letters, 2017, 19, 3512-3515
1556059 CIFC26 H22 N4P -14.8303; 9.8898; 22.174
99.193; 94.117; 98.243		1030Nallagangula, Madhu; Namitharan, Kayambu
Copper-Catalyzed Sulfonyl Azide-Alkyne Cycloaddition Reactions: Simultaneous Generation and Trapping of Copper-Triazoles and -Ketenimines for the Synthesis of Triazolopyrimidines.
Organic letters, 2017, 19, 3536-3539
1556060 CIFC20 H34 O10 SiP 1 21 19.5791; 8.5119; 15.0831
90; 100.912; 90		1207.58Fegheh-Hassanpour, Younes; Arif, Tanzeel; Sintim, Herman O.; Al Mamari, Hamad H.; Hodgson, David M.
Synthesis of (-)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition-Rearrangement and Cross-electrophile Coupling.
Organic letters, 2017, 19, 3540-3543
1556061 CIFC21 H18 Br2 O5P 1 21 110.1616; 8.0804; 12.874
90; 98.272; 90		1046.1Zhong, Xingren; Lv, Jian; Luo, Sanzhong
Enantio- and Diastereoselective Cyclopropanation of β,γ-Unsaturated α-Ketoester by a Chiral Phosphate/Indium(III) Complex.
Organic letters, 2017, 19, 3331-3334
1556062 CIFC14 H22 O2P b c a9.3826; 13.5881; 18.663
90; 90; 90		2379.38Takatori, Kazuhiko; Ota, Shoya; Tendo, Kenta; Matsunaga, Kazuma; Nagasawa, Kokoro; Watanabe, Shinya; Kishida, Atsushi; Kogen, Hiroshi; Nagaoka, Hiroto
Synthesis of Methylenebicyclo[3.2.1]octanol by a Sm(II)-Induced 1,2-Rearrangement Reaction with Ring Expansion of Methylenebicyclo[4.2.0]octanone.
Organic letters, 2017, 19, 3763-3766
1556063 CIFC19 H38 O4 S SiP 1 21 112.0435; 8.0033; 23.937
90; 102.088; 90		2256.1Santalla, Hugo; Faza, Olalla Nieto; Gómez, Generosa; Fall, Yagamare; Silva López, Carlos
From Hydrindane to Decalin: A Mild Transformation through a Dyotropic Ring Expansion.
Organic letters, 2017, 19, 3648-3651
1556064 CIFC16 H20 N2 O2P 1 21 18.6959; 9.773; 8.8762
90; 93.14; 90		753.2Wang, Jie; Wang, Lili; Guo, Shan; Zha, Shanke; Zhu, Jin
Synthesis of 2,3-Benzodiazepines via Rh(III)-Catalyzed C-H Functionalization of N-Boc Hydrazones with Diazoketoesters.
Organic letters, 2017, 19, 3640-3643
1556065 CIFC15 H18 OC 1 2/c 134.436; 8.0667; 24.298
90; 134.486; 90		4815.3Su, Naijing; Deng, Tianning; Wink, Donald J.; Driver, Tom G.
Achieving Site Selectivity in Metal-Catalyzed Electron-Rich Carbene Transfer Reactions from N-Tosylhydrazones.
Organic letters, 2017, 19, 3990-3993
1556066 CIFC20 H21 N O4 SP 1 21/n 16.949; 21.165; 12.887
90; 105.15; 90		1829.5Liu, Liu; Chen, Kun; Wu, Wen-Zhen; Wang, Peng-Fei; Song, Hang-Yu; Sun, Hongbin; Wen, Xiaoan; Xu, Qing-Long
Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals.
Organic letters, 2017, 19, 3823-3826
1556067 CIFC37 H37 Br O3P 1 21 19.4312; 11.6729; 14.7247
90; 100.851; 90		1592.1Liu, Shuai; Lan, Xin-Chan; Chen, Ke; Hao, Wen-Juan; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Ag/Brønsted Acid Co-Catalyzed Spiroketalization of β-Alkynyl Ketones toward Spiro[chromane-2,1'-isochromene] Derivatives.
Organic letters, 2017, 19, 3831-3834
1556068 CIFC36 H28 B NP 1 21/c 18.7223; 12.0422; 24.8833
90; 92.4013; 90		2611.34Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556069 CIFC46 H36 B NP 1 21/n 113.779; 10.4066; 24.1478
90; 103.533; 90		3366.47Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556070 CIFC46 H36 B NP 1 21/c 111.74; 19.9773; 15.4637
90; 110.826; 90		3389.8Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556071 CIFC30 H26 B NP 1 21/c 110.4947; 12.3025; 17.1963
90; 95.954; 90		2208.3Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556072 CIFC30 H26 B NP 1 21/n 19.1115; 14.7945; 16.9449
90; 100.664; 90		2244.7Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556073 CIFC28 H36 O8P 1 21 111.6927; 16.4378; 15.7568
90; 108.557; 90		2871.03Yin, Guo-Ping; Wu, Ya-Rong; Yang, Ming-Hua; Li, Tian-Xiao; Wang, Xiao-Bing; Zhou, Miao-Miao; Lei, Jian-Li; Kong, Ling-Yi
Citrifurans A-D, Four Dimeric Aromatic Polyketides with New Carbon Skeletons from the Fungus Aspergillus sp.
Organic letters, 2017, 19, 4058-4061
1556074 CIFC22 H26 N3 O3.5 SP 21 21 2112.3073; 18.643; 20.256
90; 90; 90		4647.6Hajra, Saumen; Singha Roy, Somnath; Aziz, Sk Mohammad; Das, Dhiraj
Catalyst-Free "On-Water" Regio- and Stereospecific Ring-Opening of Spiroaziridine Oxindole: Enantiopure Synthesis of Unsymmetrical 3,3'-Bisindoles.
Organic letters, 2017, 19, 4082-4085
1556075 CIFC20 H21 N O2P -18.8357; 10.6795; 10.7206
63.805; 75.002; 71.138		850.9Mandal, Anup; Sahoo, Harekrishna; Dana, Suman; Baidya, Mahiuddin
Ruthenium(II)-Catalyzed Hydroarylation of Maleimides Using Carboxylic Acids as a Traceless Directing Group.
Organic letters, 2017, 19, 4138-4141
1556076 CIFC17 H16 N2 O3 SP 1 21/n 110.585; 9.1046; 16.2981
90; 93.8838; 90		1567.08Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang
Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides.
Organic letters, 2017, 19, 6108-6111
1556077 CIFC15 H14 N2 O4 SP 1 21/n 110.3618; 9.18131; 15.6457
90; 90.094; 90		1488.45Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang
Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides.
Organic letters, 2017, 19, 6108-6111
1556078 CIFC14 H11 Br F N OP n a 2110.145; 26.485; 4.785
90; 90; 90		1285.7Gupta, Ekta; Kant, Ruchir; Mohanan, Kishor
Decarbethoxylative Arylation Employing Arynes: A Metal-Free Pathway to Arylfluoroamides.
Organic letters, 2017, 19, 6016-6019
1556099 CIFC49 H62 O7P -111.179; 13.411; 14.382
84.26; 83.38; 85.51		2126.2Stephan, ?; Gloe, ?; Paulus, ?; Saadioui, ?; Böhmer, V, ?
Calix Crowns Derived from para-Bridged Calix
Organic letters, 2000, 2, 839-841
1556100 CIFC13 H20 O2 SP -110.016; 11.499; 17.53
95.938; 100.417; 108.57		1854Dawid, M.; Mlostoñ, G; Warkentin, J.
The first 2,2-dialkoxythiirane.
Organic letters, 2001, 3, 2455-2456
1556101 CIFC52 H48 N4 O3P -19.935; 15.483; 15.666
66.557; 76.89; 77.978		2134.4McCarthy, Jason R.; Jenkins, Hilary A.; Brückner, Christian
Free base meso-tetraaryl-morpholinochlorins and porpholactone from meso-tetraaryl-2,3-dihydroxy-chlorin.
Organic letters, 2003, 5, 19-22
1556102 CIFC19 H18 I N O4P 21 21 219.2879; 9.8237; 19.8438
90; 90; 90		1810.6Li, Guigen; Xu, Xin; Chen, Dianjun; Timmons, Cody; Carducci, Michael D.; Headley, Allan D.
Asymmetric halo aldol reaction (AHA).
Organic letters, 2003, 5, 329-331
1556103 CIFC68 H92 Se10P -110.459; 12.983; 13.711
101.621; 96.648; 94.94		1799.9Pietschnig, Rudolf; Schäfer, Sven; Merz, Klaus
Self-addition of a sterically hindered alkynylselenolate.
Organic letters, 2003, 5, 1867-1869
1556104 CIFC19 H19 N O3 SP 1 21/c 111.0472; 7.6308; 19.6869
90; 92.423; 90		1658.1Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556105 CIFC13 H14 N2 O3P 21 21 217.572; 10.031; 15.754
90; 90; 90		1196.59Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556106 CIFC28 H16 F6 O2C c c 219.3494; 20.3274; 22.3761
90; 90; 90		8801Brizius, Glen; Billingsley, Kelvin; Smith, Mark D.; Bunz, Uwe H. F.
Conformational and electronic engineering of twisted diphenylacetylenes.
Organic letters, 2003, 5, 3951-3954
1556107 CIFC27 H40 O Si2 SnP 1 c 111.8381; 11.6026; 22.301
90; 104.522; 90		2965.2Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556108 CIFC24.6 H32.8 Cl O1.3 Si2I 41/a :233.3269; 33.3269; 9.8038
90; 90; 90		10888.9Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556109 CIFC67.5 H54.5 Br2 Cl2 N2 O6 P2 RuP 1 21 1 (c,2*a+c,b)16.649; 19.163; 27.224
90; 90; 89.58		8685.4Xu, Yingjian; Alcock, Nat W.; Clarkson, Guy J.; Docherty, Gordon; Woodward, Gary; Wills, Martin
Asymmetric hydrogenation of ketones using a ruthenium(II) catalyst containing BINOL-derived monodonor phosphorus-donor ligands.
Organic letters, 2004, 6, 4105-4107
1556110 CIFC23 H21 Br O10P 1 21 19.1105; 9.7461; 13.7386
90; 101.569; 90		1195.09Tanaka, Ken; Nishida, Goushi; Ogino, Masakazu; Hirano, Masao; Noguchi, Keiichi
Enantioselective synthesis of axially chiral biaryls through rhodium-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes.
Organic letters, 2005, 7, 3119-3121
1556111 CIFC21 H22 Cl N O5P 1 21 111.9029; 6.4499; 13.0137
90; 99.747; 90		984.67Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556112 CIFC20 H20 O5P 21 21 215.7104; 14.5249; 20.567
90; 90; 90		1705.9Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556113 CIFC7 H8 O5P 21 21 215.31; 10.8386; 12.8074
90; 90; 90		737.1Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556114 CIFC18 H20 Cl N OP 19.0186; 10.1685; 10.338
106.26; 92.413; 114.734		812.73Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi
Rhodium-catalyzed chemo-, regio-, and enantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates.
Organic letters, 2005, 7, 4737-4739
1556115 CIFC22 H19 N O2 SP 1 21 17.9578; 20.7251; 11.7791
90; 110.834; 90		1815.66Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi
Rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide.
Organic letters, 2006, 8, 907-909
1556116 CIFC24.5 H26 N O4.5 SC 1 2 125.446; 5.8028; 16.3488
90; 110.637; 90		2259.1Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao
Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides.
Organic letters, 2007, 9, 1307-1310
1556117 CIFC31 H27 N O4 SP 21 21 2110.2528; 10.7389; 47.533
90; 90; 90		5233.6Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao
Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides.
Organic letters, 2007, 9, 1307-1310
1556118 CIFC27 H31 N O4C 1 2 115.411; 10.323; 30.625
90; 103.583; 90		4736Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556119 CIFC10 H16 O3P 1 21/n 15.2334; 15.5632; 11.7443
90; 91.016; 90		956.4Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556120 CIFC20 H19 N O3P 21 21 218.715; 9.891; 19.206
90; 90; 90		1655.6Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556121 CIFC27 H29 N O3P 21 21 219.4597; 10.0663; 23.0589
90; 90; 90		2195.8Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556122 CIFC26 H31 N O3P 21 21 218.5828; 13.808; 19.023
90; 90; 90		2254.4Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556123 CIFC17 H28 Cl N Ni O SiP 1 21/n 111.287; 10.884; 15.828
90; 107.092; 90		1858.6Shrestha, Ruja; Weix, Daniel J.
Reductive conjugate addition of haloalkanes to enones to form silyl enol ethers.
Organic letters, 2011, 13, 2766-2769
1556124 CIFC26 H30 I N O5P 21 21 217.7887; 14.737; 21.142
90; 90; 90		2426.7Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J.
A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.
Organic letters, 2012, 14, 4082-4085
1556125 CIFC16 H19 N O5P 1 21 16.9621; 36.328; 6.9667
90; 117.642; 90		1560.9Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J.
A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.
Organic letters, 2012, 14, 4082-4085
1556126 CIFC26 H28 N2 O4 SP 21 21 219.6487; 12.0714; 19.866
90; 90; 90		2313.9Sequeira, Fatima C.; Chemler, Sherry R.
Stereoselective synthesis of morpholines via copper-promoted oxyamination of alkenes.
Organic letters, 2012, 14, 4482-4485
1556127 CIFC12 H12 O7P -17.8732; 7.9554; 9.7428
91.356; 108.391; 92.72		577.93Meck, Christine; Mohd, Noushad; Murelli, Ryan P.
An oxidopyrylium cyclization/ring-opening route to polysubstituted α-hydroxytropolones.
Organic letters, 2012, 14, 5988-5991
1556128 CIFC15 H20 N4 O4P 21 21 2110.49; 10.995; 13.995
90; 90; 90		1614.1Ottersbach, Philipp A.; Schmitz, Janina; Schnakenburg, Gregor; Gütschow, Michael
An access to aza-Freidinger lactams and E-locked analogs.
Organic letters, 2013, 15, 448-451
1556129 CIFC15 H23 N O3P 1 21 111.479; 16.064; 12.35
90; 101.98; 90		2227.7Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556130 CIFC13 H19 N O3P 21 21 219.917; 10.626; 11.336
90; 90; 90		1194.6Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556131 CIFC13 H19 N O3P 21 21 218.431; 11.03; 13.069
90; 90; 90		1215.3Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556132 CIFC12 H17 N O6P 21 21 218.2; 10.542; 14.773
90; 90; 90		1277Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556133 CIFC42 H46 N2 O2P -18.2943; 8.331; 13.551
101.869; 94.696; 114.24		820.9Balandier, Jean-Yves; Henry, Nicolas; Arlin, Jean-Baptiste; Sanguinet, Lionel; Lemaur, Vincent; Niebel, Claude; Chattopadhyay, Basab; Kennedy, Alan Robert; Leriche, Philippe; Blanchard, Philippe; Cornil, Jérôme; Geerts, Yves Henri
Synthesis and characterization of isomerically pure anti- and syn-anthradiindole derivatives.
Organic letters, 2013, 15, 302-305
1556134 CIFC43.82 H49.83 Cl3.45 N2 O2.67P 1 21/c 115.8497; 10.3321; 24.9736
90; 95.678; 90		4069.6Balandier, Jean-Yves; Henry, Nicolas; Arlin, Jean-Baptiste; Sanguinet, Lionel; Lemaur, Vincent; Niebel, Claude; Chattopadhyay, Basab; Kennedy, Alan Robert; Leriche, Philippe; Blanchard, Philippe; Cornil, Jérôme; Geerts, Yves Henri
Synthesis and characterization of isomerically pure anti- and syn-anthradiindole derivatives.
Organic letters, 2013, 15, 302-305
1556135 CIFC45 H28 Au2 Cl4 O4 P2P 1 21/c 110.834; 20.925; 17.732
90; 93.784; 90		4011.1Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556136 CIFC22 H13 O2 P SP -113.099; 13.122; 13.604
117.831; 117.735; 91.969		1733.1Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556137 CIFC22 H13 O3 PP b c a7.544; 17.023; 26.006
90; 90; 90		3339.7Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556138 CIFC17 H20 O5P -18.39; 9.844; 10.32
76.55; 79.16; 89.73		813.5Barluenga, José; Álvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Ángel L; Tomás, Miguel
A simple metal-promoted three-step access to n/5/m angular carbocyclic systems.
Organic letters, 2013, 15, 488-491
1556139 CIFC17 H20 O5P -18.7914; 9.2136; 10.4275
95.867; 107.824; 103.956		766.06Barluenga, José; Álvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Ángel L; Tomás, Miguel
A simple metal-promoted three-step access to n/5/m angular carbocyclic systems.
Organic letters, 2013, 15, 488-491
1556140 CIFC22 H21 Cl O4P 15.7264; 7.5889; 21.5174
91.997; 94.434; 90.306		931.69Bastida, David; Liu, Yankai; Tian, Xu; Escudero-Adán, Eduardo; Melchiorre, Paolo
Asymmetric vinylogous aldol reaction via H-bond-directing dienamine catalysis.
Organic letters, 2013, 15, 220-223
1556141 CIFC30 H25 Cl O4P 21 21 218.3789; 11.6032; 23.8284
90; 90; 90		2316.65Bastida, David; Liu, Yankai; Tian, Xu; Escudero-Adán, Eduardo; Melchiorre, Paolo
Asymmetric vinylogous aldol reaction via H-bond-directing dienamine catalysis.
Organic letters, 2013, 15, 220-223
1556142 CIFC12 H18 N2 O3 SP 21 21 215.1292; 8.5021; 28.173
90; 90; 90		1228.6Schüttler, Christian; Li-Böhmer, Zhen; Harms, Klaus; von Zezschwitz, Paultheo
Enantioselective synthesis of 3,4-disubstituted cis- and trans-1,2,5-thiadiazolidine-1,1-dioxides as precursors for chiral 1,2-diamines.
Organic letters, 2013, 15, 800-803
1556143 CIFC41 H37 Cl3 I2 N2 O9 S4P -19.3373; 15.5995; 15.8053
84.143; 86.017; 84.742		2276.3Röben, Caren; Souto, José A; Escudero-Adán, Eduardo C; Muñiz, Kilian
Oxidative diamination promoted by dinuclear iodine(III) reagents.
Organic letters, 2013, 15, 1008-1011
1556144 CIFC21 H20 F5 N O2P 21 21 217.5446; 14.193; 17.9736
90; 90; 90		1924.62Fustero, Santos; Ibáñez, Ignacio; Barrio, Pablo; Maestro, Miguel A.; Catalán, Silvia
Gold-catalyzed intramolecular hydroamination of o-alkynylbenzyl carbamates: a route to chiral fluorinated isoindoline and isoquinoline derivatives.
Organic letters, 2013, 15, 832-835
1556145 CIFC50.5 H43 Cl I N O2P 21 21 2112.6747; 15.3867; 23.8253
90; 90; 90		4646.5Liu, Yan; Shirakawa, Seiji; Maruoka, Keiji
Phase-transfer-catalyzed asymmetric conjugate cyanation of alkylidenemalonates with KCN in the presence of a Brønsted acid additive.
Organic letters, 2013, 15, 1230-1233
1556146 CIFC17 H26 N4 O3C c c 214.754; 22.06; 5.146
90; 90; 90		1674.9Rigol, Stephan; Beyer, Lothar; Hennig, Lothar; Sieler, Joachim; Giannis, Athanassios
Hünlich base: (re)discovery, synthesis, and structure elucidation after a century.
Organic letters, 2013, 15, 1418-1420
1556147 CIFC29 H28 B Fe O PP 21 21 218.9007; 14.791; 17.7255
90; 90; 90		2333.57Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556148 CIFC29 H28 B Fe O PP 21 21 219.01; 14.7132; 17.6287
90; 90; 90		2336.97Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556149 CIFC27 H32 B Fe O PP 21 21 218.9778; 9.0335; 29.5925
90; 90; 90		2399.98Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556150 CIFC27 H32 B Fe O PP 21 21 219.1406; 9.7796; 27.2445
90; 90; 90		2435.42Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556151 CIFC16 H13 N OP 1 21/c 111.237; 14.637; 7.2453
90; 99.56; 90		1175.1Liu, Le; Lu, Hang; Wang, Hong; Yang, Chao; Zhang, Xiang; Zhang-Negrerie, Daisy; Du, Yunfei; Zhao, Kang
PhI(OCOCF3)2-mediated C-C bond formation concomitant with a 1,2-aryl shift in a metal-free synthesis of 3-arylquinolin-2-ones.
Organic letters, 2013, 15, 2906-2909
1556152 CIFC56 H48 F8 N4P -18.695; 9.355; 13.874
104.83; 90.259; 90.583		1090.9Takase, Masayoshi; Inabe, Ayumi; Sugawara, Yuki; Fujita, Wataru; Nishinaga, Tohru; Nomura, Kotohiro
Donor-acceptor segregated paracyclophanes composed of naphthobipyrrole and stacked fluoroarenes.
Organic letters, 2013, 15, 3202-3205
1556153 CIFC40 H20 F8 N4C 1 2/c 120.8969; 25.977; 14.1722
90; 129.736; 90		5916.1Takase, Masayoshi; Inabe, Ayumi; Sugawara, Yuki; Fujita, Wataru; Nishinaga, Tohru; Nomura, Kotohiro
Donor-acceptor segregated paracyclophanes composed of naphthobipyrrole and stacked fluoroarenes.
Organic letters, 2013, 15, 3202-3205
1556154 CIFC18 H14 O3P 1 21/n 15.5563; 23.1971; 10.5069
90; 96.804; 90		1344.7Yang, Yuzhu; Yao, Jinzhong; Zhang, Yuhong
Synthesis of polysubstituted furans via copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids.
Organic letters, 2013, 15, 3206-3209
1556155 CIFC20 H21 Cl N O RhP b c a15.6316; 14.9322; 15.632
90; 90; 90		3648.7Zhou, Bing; Du, Juanjuan; Yang, Yaxi; Li, Yuanchao
Rhodium(III)-catalyzed intermolecular direct amidation of aldehyde C-H bonds with N-chloroamines at room temperature.
Organic letters, 2013, 15, 2934-2937
1556156 CIFC16 H19 F6 I O6 S2P -17.9401; 11.866; 12.2428
89.151; 82.917; 83.972		1138.35Saito, Akio; Taniguchi, Akihiro; Kambara, Yui; Hanzawa, Yuji
Metal-free [2 + 2 + 1] annulation of alkynes, nitriles, and oxygen atoms: iodine(III)-mediated synthesis of highly substituted oxazoles.
Organic letters, 2013, 15, 2672-2675
1556157 CIFC58 H40 N4P -19.5556; 10.9143; 21.922
95.336; 99.004; 114.209		2028Mutoh, Katsuya; Shima, Kentaro; Yamaguchi, Tetsuo; Kobayashi, Masayuki; Abe, Jiro
Photochromism of a naphthalene-bridged imidazole dimer constrained to the "anti" conformation.
Organic letters, 2013, 15, 2938-2941
1556158 CIFC20 H20 O6P 21 21 2110.0241; 10.2749; 16.6432
90; 90; 90		1714.19Bautista, Elihú; Toscano, Rubén Alfredo; Ortega, Alfredo
Microphyllandiolide, a new diterpene with an unprecedented skeleton from Salvia microphylla.
Organic letters, 2013, 15, 3210-3213
1556159 CIFC21 H20 F N3 OP 1 21 17.1383; 10.6018; 12.0383
90; 102.375; 90		889.876Aillaud, Isabelle; Barber, David M.; Thompson, Amber L.; Dixon, Darren J.
Enantioselective Michael addition/iminium ion cyclization cascades of tryptamine-derived ureas.
Organic letters, 2013, 15, 2946-2949
1556160 CIFC23 H35 Cl2 F N2 O3 SiP -19.2544; 10.1036; 14.037
89.263; 76.663; 84.842		1271.89Shupe, Benjamin H.; Allen, Emily E.; MacDonald, Jacob P.; Wilson, Sean O.; Franz, Annaliese K.
Synthesis of spirocarbamate oxindoles via intramolecular trapping of a β-silyl carbocation by an N-Boc group.
Organic letters, 2013, 15, 3218-3221
1556161 CIFC12 H9 Cl O4P 1 21/c 19.5934; 34.977; 6.9856
90; 111.154; 90		2186.1Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556162 CIFC24 H22 O6P 6519.1393; 19.1393; 10.2697
90; 90; 120		3257.92Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556163 CIFC13 H12 O5P 1 21/n 18.0607; 12.2714; 11.6095
90; 91.224; 90		1148.1Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556164 CIFC36 H40 Si3P -19.8245; 10.2504; 17.1303
98.958; 106.078; 97.745		1608.4Kinoshita, Hidenori; Takahashi, Hirotoshi; Miura, Katsukiyo
Regioselective synthesis of multisubstituted benzenes by palladium-catalyzed intermolecular reaction of β-iodo-β-silylstyrenes with alkynes.
Organic letters, 2013, 15, 2962-2965
1556165 CIFC37 H30 SiP 1 21/n 110.6578; 14.5155; 39.626
90; 91.372; 90		6128.5Kinoshita, Hidenori; Takahashi, Hirotoshi; Miura, Katsukiyo
Regioselective synthesis of multisubstituted benzenes by palladium-catalyzed intermolecular reaction of β-iodo-β-silylstyrenes with alkynes.
Organic letters, 2013, 15, 2962-2965
1556166 CIFC17 H24 N2 O SiP 1 21/n 113.2419; 8.6081; 15.4864
90; 109.76; 90		1661.3Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556167 CIFC16 H28 N2 O3 SiP 21 21 216.6646; 8.5137; 30.7646
90; 90; 90		1745.6Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556168 CIFC21 H30 N2 O SiP 1 21/c 18.4425; 13.9418; 17.4523
90; 91.014; 90		2053.9Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556169 CIFC12 H20 N2 O SiP 1 21 16.1243; 7.9668; 12.884
90; 98.931; 90		621Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556170 CIFC16 H10 N2 O2P 1 21/n 17.49; 14.7964; 11.472
90; 107.785; 90		1210.6Wang, Chen; Zhang, Lianpeng; Ren, Anni; Lu, Ping; Wang, Yanguang
Cu-catalyzed synthesis of tryptanthrin derivatives from substituted indoles.
Organic letters, 2013, 15, 2982-2985
1556171 CIFC27 H24 O3 SP -18.856; 11.3252; 12.3448
109.775; 92.023; 112.173		1059.92Chang, Meng-Yang; Wu, Ming-Hao; Chen, Yeh-Long
One-pot synthesis of substituted tetrahydrocyclobuta[a]naphthalenes by domino aldol condensation/olefin migration/electrocyclization.
Organic letters, 2013, 15, 2822-2825
1556172 CIFC19 H23 N OP 1 21 16.1008; 7.6894; 17.0974
90; 99.543; 90		790.97Hansmann, Max M.; Hashmi, A Stephen K; Lautens, Mark
Gold meets rhodium: tandem one-pot synthesis of β-disubstituted ketones via Meyer-Schuster rearrangement and asymmetric 1,4-addition.
Organic letters, 2013, 15, 3226-3229
1556173 CIFC23 H21 Br OP 21 21 2110.0001; 10.0316; 19.1693
90; 90; 90		1923.01Hansmann, Max M.; Hashmi, A Stephen K; Lautens, Mark
Gold meets rhodium: tandem one-pot synthesis of β-disubstituted ketones via Meyer-Schuster rearrangement and asymmetric 1,4-addition.
Organic letters, 2013, 15, 3226-3229
1556174 CIFC21 H21 N O2P 1 21/c 19.4044; 19.072; 18.984
90; 101.853; 90		3332.4Chen, Te-Yu; Krische, Michael J.
Regioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: prenylation, geranylation, and beyond.
Organic letters, 2013, 15, 2994-2997
1556175 CIFC17 H16 N2 O3 SP 1 21/c 112.587; 8.748; 14.954
90; 90.12; 90		1646.6Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556176 CIFC25 H19 N3 O3C 1 2/c 118.0952; 10.2372; 21.8977
90; 94.54; 90		4043.7Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556177 CIFC25 H20 N2 OP 1 21/c 111.075; 10.665; 16.846
90; 100.97; 90		1953.4Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556178 CIFC23 H21 N O SP -18.957; 12.165; 17.911
90.195; 104.25; 90.15		1891.5Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556179 CIFC20 H18 N2 O2P 1 21/c 113.639; 10.357; 12.061
90; 106.519; 90		1633.4Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556180 CIFC24 H19 N3 O3P -19.0832; 10.4022; 11.9282
69; 81.227; 83.991		1038.34Ramachary, D. B.; Venkaiah, Chintalapudi; Madhavachary, R.
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis.
Organic letters, 2013, 15, 3042-3045
1556181 CIFC21 H12 Cl N3 O2P 21 21 216.7978; 13.7806; 19.1936
90; 90; 90		1798.01Ramachary, D. B.; Venkaiah, Chintalapudi; Madhavachary, R.
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis.
Organic letters, 2013, 15, 3042-3045
1556182 CIFC28 H22 O4P 1 21/c 114.431; 8.092; 36.817
90; 91.972; 90		4297Li, Erqing; Huang, You; Liang, Ling; Xie, Peizhong
Phosphine-catalyzed [4 + 2] annulation of γ-substituent allenoates: facile access to functionalized spirocyclic skeletons.
Organic letters, 2013, 15, 3138-3141
1556183 CIFC20 H32 O5P 43 21 29.653; 9.653; 40.391
90; 90; 90		3763.6Zhang, Mengke; Zhu, Yan; Zhan, Guanqun; Shu, Penghua; Sa, Rongjian; Lei, Liang; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Wan, Qian; Yao, Guangmin; Zhang, Yonghui
Micranthanone A, a new diterpene with an unprecedented carbon skeleton from Rhododendron micranthum.
Organic letters, 2013, 15, 3094-3097
1556184 CIFC31 H44 O9P 21 21 219.2161; 14.354; 21.9606
90; 90; 90		2905.12Zhang, Mengke; Zhu, Yan; Zhan, Guanqun; Shu, Penghua; Sa, Rongjian; Lei, Liang; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Wan, Qian; Yao, Guangmin; Zhang, Yonghui
Micranthanone A, a new diterpene with an unprecedented carbon skeleton from Rhododendron micranthum.
Organic letters, 2013, 15, 3094-3097
1556185 CIFC17 H17 Br O4P -16.1044; 9.3857; 14.7205
78.9278; 79.0335; 82.9068		809.27Woodall, Erica L.; Simanis, Justin A.; Hamaker, Christopher G.; Goodell, John R.; Mitchell, T. Andrew
Unique reactivity of anti- and syn-acetoxypyranones en route to oxidopyrylium intermediates leading to a cascade process.
Organic letters, 2013, 15, 3270-3273
1556186 CIFC37 H40 Cl N5 O2P 21 21 219.439; 13.768; 26.584
90; 90; 90		3455Zou, Liwei; Wang, Baomin; Mu, Hongfang; Zhang, Huanrui; Song, Yuming; Qu, Jingping
Development of tartaric acid derived chiral guanidines and their application to catalytic enantioselective α-hydroxylation of β-dicarbonyl compounds.
Organic letters, 2013, 15, 3106-3109
1556187 CIFC34 H26 F N O4 S2P 1 21 19.5437; 15.151; 10.6193
90; 111.641; 90		1427.3Matsuzaki, Kohei; Furukawa, Tatsuya; Tokunaga, Etsuko; Matsumoto, Takashi; Shiro, Motoo; Shibata, Norio
Highly enantioselective monofluoromethylation of C2-arylindoles using FBSM under chiral phase-transfer catalysis.
Organic letters, 2013, 15, 3282-3285
1556188 CIFC40.6 H39.25 Cl0.35 F5 N1.5 O4P -16.872; 22.864; 25.039
70.46; 85.66; 76.63		3607Ito, Satoru; Hiroto, Satoru; Shinokubo, Hiroshi
Synthesis of pyridine-fused perylene imides with an amidine moiety for hydrogen bonding.
Organic letters, 2013, 15, 3110-3113
1556189 CIFC24 H26 O4P 1 21 16.2434; 8.0127; 21.1301
90; 90.262; 90		1057.05Ni, Shengjun; Chen, Jie; Ma, Shengming
Unexpected regioselectivity switch: organophosphine-triggered reactions of cyclopropene-1,1-dicarboxylates with aldehydes.
Organic letters, 2013, 15, 3290-3293
1556190 CIFC28 H33 B O2 SiP -110.0966; 10.7209; 13.1753
94.573; 94.171; 109.28		1334.4Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556191 CIFC28 H40 B2 O4 SiP -19.6731; 12.2468; 13.2905
106.215; 91.906; 104.067		1457.8Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556192 CIFC29 H20 F3 N OP -110.299; 12.07; 19.582
89.885; 86.412; 78.391		2379.6Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556193 CIFC30 H26 Br2 O5P 1 21/n 19.8739; 19.0209; 13.9849
90; 94.282; 90		2619.2Yeom, Hyun-Suk; Li, Hui; Tang, Yu; Hsung, Richard P.
Total syntheses of cannabicyclol, clusiacyclol A and B, iso-eriobrucinol A and B, and eriobrucinol.
Organic letters, 2013, 15, 3130-3133
1556194 CIFC16 H20 O3F d d 224.479; 35.736; 6.333
90; 90; 90		5540Yeom, Hyun-Suk; Li, Hui; Tang, Yu; Hsung, Richard P.
Total syntheses of cannabicyclol, clusiacyclol A and B, iso-eriobrucinol A and B, and eriobrucinol.
Organic letters, 2013, 15, 3130-3133
1556195 CIFC16 H10 F3 NP 1 21/c 114.393; 4.9376; 17.802
90; 101.306; 90		1240.6Tiwari, Virendra Kumar; Pawar, Govind Goroba; Das, Riki; Adhikary, Amit; Kapur, Manmohan
Heteroatom-guided, palladium-catalyzed regioselective C-H functionalization in the synthesis of 3-arylquinolines.
Organic letters, 2013, 15, 3310-3313
1556196 CIFC29 H31 B N2 O2P 1 c 111.3125; 9.5581; 12.1929
90; 111.496; 90		1226.66Shaban Ragab, Sherif; Swaminathan, Subramani; Deniz, Erhan; Captain, Burjor; Raymo, Françisco M
Fluorescence photoactivation by ligand exchange around the boron center of a BODIPY chromophore.
Organic letters, 2013, 15, 3154-3157
1556197 CIFC18 H16 N2 O2P 1 21/c 111.1596; 9.7432; 13.8929
90; 102.558; 90		1474.44Chun, Yu Sung; Xuan, Zi; Kim, Ju Hyun; Lee, Sang-gi
An expedient and divergent tandem one-pot synthesis of pyrimidin-2,4-diones using the Blaise reaction intermediate.
Organic letters, 2013, 15, 3162-3165
1556198 CIFC20 H20 O3 SP 1 21 18.1366; 12.602; 9.5079
90; 110.672; 90		912.15Shirakawa, Seiji; Tokuda, Takashi; Kasai, Atsuyuki; Maruoka, Keiji
Design of chiral bifunctional quaternary phosphonium bromide catalysts possessing an amide moiety.
Organic letters, 2013, 15, 3350-3353
1556199 CIFC14 H14 F3 N O5P 1 21/c 19.0022; 12.1545; 13.6525
90; 101.948; 90		1461.46Molander, Gary A.; Cavalcanti, Livia N.
Synthesis of trifluoromethylated isoxazolidines: 1,3-dipolar cycloaddition of nitrosoarenes, (trifluoromethyl)diazomethane, and alkenes.
Organic letters, 2013, 15, 3166-3169
1556200 CIFC23 H18 F3 N O2P 1 21/c 120.4457; 19.4232; 9.4746
90; 90.583; 90		3762.4Molander, Gary A.; Cavalcanti, Livia N.
Synthesis of trifluoromethylated isoxazolidines: 1,3-dipolar cycloaddition of nitrosoarenes, (trifluoromethyl)diazomethane, and alkenes.
Organic letters, 2013, 15, 3166-3169
1556201 CIFC11 H9 N O3P 1 21/c 17.2107; 11.437; 11.361
90; 98.05; 90		927.7Maity, Soham; Naveen, Togati; Sharma, Upendra; Maiti, Debabrata
Stereoselective nitration of olefins with (t)BuONO and TEMPO: direct access to nitroolefins under metal-free conditions.
Organic letters, 2013, 15, 3384-3387
1556202 CIFC100 H150 Cl4 P4P 1 21/n 122.2024; 16.1149; 27.8962
90; 103.284; 90		9713.9Ito, Shigekazu; Kobayashi, Makoto; Mikami, Koichi
Through-space electrostatic interaction between the electron-donating 1,3-diphosphacyclobutane-2,4-diyl units.
Organic letters, 2013, 15, 3404-3407
1556203 CIFC25 H42 O5 SiP 1 21/c 124.5119; 11.5268; 10.5087
90; 120.735; 90		2552.1Kreuzer, Andreas; Kerres, Sabine; Ertl, Thomas; Rücker, Hannelore; Amslinger, Sabine; Reiser, Oliver
Asymmetric synthesis of both enantiomers of arteludovicinolide A.
Organic letters, 2013, 15, 3420-3423
1556204 CIFC23 H38 O5 SiP 21 21 218.16912; 14.1495; 20.6305
90; 90; 90		2384.66Kreuzer, Andreas; Kerres, Sabine; Ertl, Thomas; Rücker, Hannelore; Amslinger, Sabine; Reiser, Oliver
Asymmetric synthesis of both enantiomers of arteludovicinolide A.
Organic letters, 2013, 15, 3420-3423
1556205 CIFC16 H21 Cl N2 O3P 21 21 219.8721; 10.1397; 16.1579
90; 90; 90		1617.4Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
Enantioselective hydroarylation of bridged [3.2.1] heterocycles: an efficient entry into the homoepibatidine skeleton.
Organic letters, 2013, 15, 3424-3427
1556206 CIFC16 H21 Cl N2 O3P 21 21 219.9446; 10.3967; 16.1629
90; 90; 90		1671.1Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
Enantioselective hydroarylation of bridged [3.2.1] heterocycles: an efficient entry into the homoepibatidine skeleton.
Organic letters, 2013, 15, 3424-3427
1556207 CIFC26 H25 N3 O3P -17.5683; 11.9057; 14.1137
102.206; 101.521; 92.584		1212.9Lee, Boram; Chen, Shiyu; Heinis, Christian; Scopelliti, Rosario; Severin, Kay
Pattern-based sensing of peptides and aminoglycosides with a single molecular probe.
Organic letters, 2013, 15, 3456-3459
1556208 CIFC38 H41 N5 O3P -110.1792; 11.8174; 13.9668
90.426; 90.494; 102.848		1637.9Lee, Boram; Chen, Shiyu; Heinis, Christian; Scopelliti, Rosario; Severin, Kay
Pattern-based sensing of peptides and aminoglycosides with a single molecular probe.
Organic letters, 2013, 15, 3456-3459
1556209 CIFC27 H22 N2C 1 2/c 135.073; 8.211; 14.159
90; 106.809; 90		3903.4Zhu, Xu; Wang, Yi-Feng; Ren, Wei; Zhang, Feng-Lian; Chiba, Shunsuke
TEMPO-mediated aliphatic C-H oxidation with oximes and hydrazones.
Organic letters, 2013, 15, 3214-3217
1556210 CIFC28 H22 N2 OP -110.7757; 11.1883; 19.7287
80.672; 74.688; 68.604		2130.3Zhu, Xu; Wang, Yi-Feng; Ren, Wei; Zhang, Feng-Lian; Chiba, Shunsuke
TEMPO-mediated aliphatic C-H oxidation with oximes and hydrazones.
Organic letters, 2013, 15, 3214-3217
1556211 CIFC24 H24 N2 O5 SP 1 21 110.107; 6.8488; 16.9251
90; 90.667; 90		1171.49Meninno, Sara; Croce, Gianluca; Lattanzi, Alessandra
Asymmetric synthesis of trisubstituted tetrahydrothiophenes bearing a quaternary stereocenter via double Michael reaction involving dynamic kinetic resolution.
Organic letters, 2013, 15, 3436-3439
1556212 CIFC28 H33 N O3 SP -111.835; 11.975; 12.118
61.205; 84.631; 63.739		1334Meninno, Sara; Croce, Gianluca; Lattanzi, Alessandra
Asymmetric synthesis of trisubstituted tetrahydrothiophenes bearing a quaternary stereocenter via double Michael reaction involving dynamic kinetic resolution.
Organic letters, 2013, 15, 3436-3439
1556213 CIFC13 H8 N2 O2P b c a12.6783; 7.099; 23.032
90; 90; 90		2073Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556214 CIFC17 H18 Br N2 Na O5P 1 21/c 113.7372; 18.5165; 7.4853
90; 97.958; 90		1885.66Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556215 CIFC14 H10 N2 O3P -17.3116; 15.2786; 16.3552
105.854; 95.436; 95.125		1736.9Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556216 CIFC28 H23 N O3P -18.584; 11.098; 12.526
71.237; 74.269; 80.711		1083.9Yang, Min; Tang, Jie; Fan, Renhua
Dearomatization strategy of β-enamino ester: construction of indenoazepines via tandem Michael addition/polycyclization.
Organic letters, 2013, 15, 3464-3467
1556217 CIFC30 H29 N O5 SP 1 21/c 119.519; 7.83; 18.538
90; 114.675; 90		2574.5Yang, Min; Tang, Jie; Fan, Renhua
Dearomatization strategy of β-enamino ester: construction of indenoazepines via tandem Michael addition/polycyclization.
Organic letters, 2013, 15, 3464-3467
1556218 CIFC10 H12 N2 O3P b c a7.4941; 15.8862; 16.1019
90; 90; 90		1916.98de Robillard, Guillaume; Devillers, Charles H.; Kunz, Doris; Cattey, Hélène; Digard, Eric; Andrieu, Jacques
Electrosynthesis of imidazolium carboxylates.
Organic letters, 2013, 15, 4410-4413
1556219 CIFC9 H13 Cl N2 OP 1 21/c 18.6471; 16.9091; 7.308
90; 111.426; 90		994.69de Robillard, Guillaume; Devillers, Charles H.; Kunz, Doris; Cattey, Hélène; Digard, Eric; Andrieu, Jacques
Electrosynthesis of imidazolium carboxylates.
Organic letters, 2013, 15, 4410-4413
1556220 CIFC32 H37 Br O5P 21 21 216.161; 19.878; 23.992
90; 90; 90		2938.3Ma, Shuang-Gang; Gao, Rong-Mei; Li, Yu-Huan; Jiang, Jian-Dong; Gong, Ning-Bo; Li, Li; Lü, Yang; Tang, Wen-Zhao; Liu, Yun-Bao; Qu, Jing; Lü, Hai-Ning; Li, Yong; Yu, Shi-Shan
Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum.
Organic letters, 2013, 15, 4450-4453
1556221 CIFC32 H37 Br O5P 15.9898; 9.7098; 12.2465
90.307; 91.544; 99.152		702.9Ma, Shuang-Gang; Gao, Rong-Mei; Li, Yu-Huan; Jiang, Jian-Dong; Gong, Ning-Bo; Li, Li; Lü, Yang; Tang, Wen-Zhao; Liu, Yun-Bao; Qu, Jing; Lü, Hai-Ning; Li, Yong; Yu, Shi-Shan
Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum.
Organic letters, 2013, 15, 4450-4453

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 11 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.