Crystallography Open Database

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Searching journal of publication like 'Organic Letters'

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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 CIFC11 H9 F0.5 N0.5 O1.5P -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 CIFC16 H18.18 N2.18 O2.55 S0.73P 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

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