Crystallography Open Database

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Searching journal of publication like 'Organic Letters'

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1547051 CIFC33 H42 O8P 21 21 219.5408; 16.3122; 18.8674
90; 90; 90
2936.36An, Fa-Liang; Sun, Dong-Mei; Li, Rui-Jun; Zhou, Miao-Miao; Yang, Ming-Hua; Yin, Yong; Kong, Ling-Yi; Luo, Jun
Walrobsins A and B, Two Anti-inflammatory Limonoids from Root Barks of Walsura robusta.
Organic letters, 2017, 19, 4568-4571
1547052 CIFC33 H44 O8P 21 21 219.434; 16.4028; 19.4128
90; 90; 90
3004.01An, Fa-Liang; Sun, Dong-Mei; Li, Rui-Jun; Zhou, Miao-Miao; Yang, Ming-Hua; Yin, Yong; Kong, Ling-Yi; Luo, Jun
Walrobsins A and B, Two Anti-inflammatory Limonoids from Root Barks of Walsura robusta.
Organic letters, 2017, 19, 4568-4571
1547053 CIFC13 H18 N2 O5C 1 2/c 125.2209; 7.4847; 17.0575
90; 119.615; 90
2799.3Li, Zhengning; Lam, Shuk Mei; Ip, Ignatius; Wong, Wing-Tak; Chiu, Pauline
Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones.
Organic letters, 2017, 19, 4464-4467
1547054 CIFC11 H16 N2 O2P c a 2124.608; 7.147; 12.285
90; 90; 90
2160.6Li, Zhengning; Lam, Shuk Mei; Ip, Ignatius; Wong, Wing-Tak; Chiu, Pauline
Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones.
Organic letters, 2017, 19, 4464-4467
1547055 CIFC13 H18 N2 O4P -17.536; 8.9321; 10.4173
103.152; 95.411; 90.804
679.32Li, Zhengning; Lam, Shuk Mei; Ip, Ignatius; Wong, Wing-Tak; Chiu, Pauline
Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones.
Organic letters, 2017, 19, 4464-4467
1547056 CIFC13 H18 O5P 1 21/c 16.2449; 16.6852; 13.0222
90; 92.659; 90
1355.42Li, Zhengning; Lam, Shuk Mei; Ip, Ignatius; Wong, Wing-Tak; Chiu, Pauline
Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones.
Organic letters, 2017, 19, 4464-4467
1547057 CIFC13 H17 N O2 SP 21 21 216.133; 10.094; 20.181
90; 90; 90
1249.3Li, Yuewen; Mao, Runyu; Wu, Jie
N-Radical Initiated Aminosulfonylation of Unactivated C(sp(3))-H Bond through Insertion of Sulfur Dioxide.
Organic letters, 2017, 19, 4472-4475
1547058 CIFC24 H18 Cl4 N2 O4 SP 1 21/c 112.3024; 11.6242; 18.662
90; 101.576; 90
2614.5Meng, Jiang; Jia, Renmeng; Leng, Jiaying; Wen, Min; Yu, Xingxin; Deng, Wei-Ping
Carbon-Carbon Bond Formation by Reaction of Rhodium Azavinylcarbenes with Secondary Amides: Access to Indigo Analogues from Isatins.
Organic letters, 2017, 19, 4520-4523
1547059 CIFC18 H15 Br O5P 1 21 16.5833; 9.956; 24.64
90; 95.324; 90
1608Shi, Li-Min; Dong, Wu-Wei; Tao, Hai-Yan; Dong, Xiu-Qin; Wang, Chun-Jiang
Catalytic Asymmetric Desymmetrization of Cyclopentendiones via Diels-Alder Reaction of 3-Hydroxy-2-pyrones: Construction of Multifunctional Bridged Tricyclic Lactones.
Organic letters, 2017, 19, 4532-4535
1547060 CIFC18 H23 Br O5P -15.2059; 10.5536; 16.861
99.88; 95.519; 92.866
906.3Lam, Shuk Mei; Wong, Wing-Tak; Chiu, Pauline
An Approach to the Welwistatin Core via a Diazoketone Rearrangement-Ring Expansion Strategy.
Organic letters, 2017, 19, 4468-4471
1547061 CIFC16 H16 O4P 1 21/c 112.2416; 15.1877; 7.6373
90; 94.46; 90
1415.64Lam, Shuk Mei; Wong, Wing-Tak; Chiu, Pauline
An Approach to the Welwistatin Core via a Diazoketone Rearrangement-Ring Expansion Strategy.
Organic letters, 2017, 19, 4468-4471
1547062 CIFC16 H15 Br O4P c c n15.6419; 23.9707; 7.8208
90; 90; 90
2932.4Lam, Shuk Mei; Wong, Wing-Tak; Chiu, Pauline
An Approach to the Welwistatin Core via a Diazoketone Rearrangement-Ring Expansion Strategy.
Organic letters, 2017, 19, 4468-4471
1547063 CIFC32 H25 N3 O4P 21 21 219.9278; 13.8213; 19.0453
90; 90; 90
2613.3Mondal, Santigopal; Mukherjee, Subrata; Yetra, Santhivardhana Reddy; Gonnade, Rajesh G.; Biju, Akkattu T.
Organocatalytic Enantioselective Vinylogous Michael-Aldol Cascade for the Synthesis of Spirocyclic Compounds.
Organic letters, 2017, 19, 4367-4370
1547064 CIFC102.5 H75.5 Cl12.75 N6P 1 21/c 124.334; 13.557; 27.189
90; 90.828; 90
8969Kurata, Ryohei; Sakamaki, Daisuke; Uebe, Masashi; Kinoshita, Mariko; Iwanaga, Tetsuo; Matsumoto, Takashi; Ito, Akihiro
Isolable Triradical Trication of Hexaaza[16]paracyclophane with Embedded 9,10-Anthrylenes: A Frustrated Three-Spin System.
Organic letters, 2017, 19, 4371-4374
1547065 CIFC132 H138 N6 O6P -112.217; 20.357; 22.761
74.897; 85.716; 85.813
5441Kurata, Ryohei; Sakamaki, Daisuke; Uebe, Masashi; Kinoshita, Mariko; Iwanaga, Tetsuo; Matsumoto, Takashi; Ito, Akihiro
Isolable Triradical Trication of Hexaaza[16]paracyclophane with Embedded 9,10-Anthrylenes: A Frustrated Three-Spin System.
Organic letters, 2017, 19, 4371-4374
1547066 CIFC213.35 H122.46 B3 Cl0.88 F60 N6 O7P 1 21/n 116.3119; 24.2584; 46.9151
90; 93.504; 90
18529.6Kurata, Ryohei; Sakamaki, Daisuke; Uebe, Masashi; Kinoshita, Mariko; Iwanaga, Tetsuo; Matsumoto, Takashi; Ito, Akihiro
Isolable Triradical Trication of Hexaaza[16]paracyclophane with Embedded 9,10-Anthrylenes: A Frustrated Three-Spin System.
Organic letters, 2017, 19, 4371-4374
1547067 CIFC38 H40 F6 N2 O6 Pd2C 1 2/c 130.1441; 16.1678; 21.0618
90; 121.245; 90
8775.9Maraswami, Manikantha; Pankajakshan, Sreekumar; Chen, Gang; Loh, Teck-Peng
Palladium-Catalyzed Direct C-H Trifluoroethylation of Aromatic Amides.
Organic letters, 2017, 19, 4223-4226
1547068 CIFC26 H25 N O9P 1 21 19.04; 6.791; 19.479
90; 95.016; 90
1191.2Gheewala, Chirag D.; Radtke, M. Alex; Hui, Jessica; Hon, Alec B.; Lambert, Tristan H.
Methods for the Synthesis of Functionalized Pentacarboxycyclopentadienes.
Organic letters, 2017, 19, 4227-4230
1547069 CIFC38 H35 Cl3 N2 O8P 21 21 216.3428; 21.435; 25.73
90; 90; 90
3498.2Gheewala, Chirag D.; Radtke, M. Alex; Hui, Jessica; Hon, Alec B.; Lambert, Tristan H.
Methods for the Synthesis of Functionalized Pentacarboxycyclopentadienes.
Organic letters, 2017, 19, 4227-4230
1547070 CIFC21 H14 N2 O3 SP -18.6027; 14.6659; 14.8286
82.014; 77.654; 76.926
1772.1Lan, Jianyong; Xie, Haisheng; Lu, Xiaoxia; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Co(II)-Catalyzed Regioselective Cross-Dehydrogenative Coupling of Aryl C-H Bonds with Carboxylic Acids.
Organic letters, 2017, 19, 4279-4282
1547071 CIFC18 H19 I N2P 1 21/n 112.7416; 15.7164; 16.1249
90; 90.844; 90
3228.69Zhu, Dao-Yong; Fang, Lei; Han, Hui; Wang, Yazhou; Xia, Ji-Bao
Reductive CO2 Fixation via Tandem C-C and C-N Bond Formation: Synthesis of Spiro-indolepyrrolidines.
Organic letters, 2017, 19, 4259-4262
1547072 CIFC29 H22 O3P -19.229; 11.78; 11.881
116.064; 93.344; 103.846
1106.6Sicignano, Marina; Dentoni Litta, Antonella; Schettini, Rosaria; De Riccardis, Francesco; Pierri, Giovanni; Tedesco, Consiglia; Izzo, Irene; Della Sala, Giorgio
Highly Diastereoselective Crown Ether Catalyzed Arylogous Michael Reaction of 3-Aryl Phthalides.
Organic letters, 2017, 19, 4383-4386
1547073 CIFC28 H26 O6P -111.5473; 11.75; 18.402
78.259; 74.402; 88.332
2353.7Sicignano, Marina; Dentoni Litta, Antonella; Schettini, Rosaria; De Riccardis, Francesco; Pierri, Giovanni; Tedesco, Consiglia; Izzo, Irene; Della Sala, Giorgio
Highly Diastereoselective Crown Ether Catalyzed Arylogous Michael Reaction of 3-Aryl Phthalides.
Organic letters, 2017, 19, 4383-4386
1547074 CIFC21 H29 Br N2 O3 SC 1 2/c 137.0871; 18.9011; 13.1357
90; 106.015; 90
8850.6Abe, Takumi; Suzuki, Takuro; Anada, Masahiro; Matsunaga, Shigeki; Yamada, Koji
2-Hydroxyindoline-3-triethylammonium Bromide: A Reagent for Formal C3-Electrophilic Reactions of Indoles.
Organic letters, 2017, 19, 4275-4278
1547075 CIFC20 H14 Cl N OP 1 21/c 18.1638; 14.323; 13.4195
90; 107.745; 90
1494.5Kumar, Tarun; Mane, Vaijinath; Namboothiri, Irishi N. N.
Synthesis of Aminophenanthrenes and Benzoquinolines via Hauser-Kraus Annulation of Sulfonyl Phthalide with Rauhut-Currier Adducts of Nitroalkenes.
Organic letters, 2017, 19, 4283-4286
1547076 CIFC28 H54 B Fe N O2 P2C 2 2 2112.9849; 18.5848; 26.1432
90; 90; 90
6308.9Nakajima, Kazunari; Kato, Takeru; Nishibayashi, Yoshiaki
Hydroboration of Alkynes Catalyzed by Pyrrolide-Based PNP Pincer-Iron Complexes.
Organic letters, 2017, 19, 4323-4326
1547077 CIFC30 H24 O6P 1 21 111.7456; 16.9831; 12.0924
90; 94.193; 90
2405.7Zhang, Lan-Jun; Bi, De-Wen; Hu, Jiangmiao; Mu, Wei-Hua; Li, Yuan-Ping; Xia, Guang-Hui; Yang, Liu; Li, Xiao-Nian; Liang, Xue-Song; Wang, Li-Qin
Four Hybrid Flavan-Chalcones, Caesalpinnone A Possessing a 10,11-Dioxatricyclic [5.3.3.0(1,6)]Tridecane-Bridged System and Caesalpinflavans A-C from Caesalpinia enneaphylla.
Organic letters, 2017, 19, 4315-4318
1547078 CIFC18 H15 N OP 1 21/c 19.098; 12.686; 12.465
90; 104.57; 90
1392.4Geng, Xiao; Wu, Xia; Zhao, Peng; Zhang, Jingjing; Wu, Yan-Dong; Wu, An-Xin
Synergistic I2/Amine Promoted Povarov-Type Reaction for the Synthesis of 2-Acyl-3-aryl(alkyl)quinolines Using Aryl(alkyl)acetaldehydes as Alkene Surrogates.
Organic letters, 2017, 19, 4179-4182
1547079 CIFC22 H26 N2 O3 SP 21 21 215.6401; 15.5044; 23.257
90; 90; 90
2033.7Li, Kangnan; Weber, Alexandria E.; Tseng, Luke; Malcolmson, Steven J.
Diastereoselective and Enantiospecific Synthesis of 1,3-Diamines via 2-Azaallyl Anion Benzylic Ring-Opening of Aziridines.
Organic letters, 2017, 19, 4239-4242
1547080 CIFC19 H22 O2 S2P 1 21/c 111.401; 9.001; 17.228
90; 100.234; 90
1739.8Lvov, Andrey G.; Milevsky, Nikita A.; Yanina, Anna M.; Kachala, Vadim V.; Shirinian, Valerii Z.
Aerobic Dimerization of Ethyl 4-Thienyl-3-ketobutanoate toward a Modifiable Photochromic Diarylethene Precursor.
Organic letters, 2017, 19, 4395-4398
1547081 CIFC17 H18 N4 O3P 18.8973; 10.3854; 10.5682
113.149; 92.819; 112.907
803.17Bernar, Ivan; Fiser, Béla; Blanco-Ania, Daniel; Gómez-Bengoa, Enrique; Rutjes, Floris P. J. T.
Pd-Catalyzed Hydroamination of Alkoxyallenes with Azole Heterocycles: Examples and Mechanistic Proposal.
Organic letters, 2017, 19, 4211-4214
1547082 CIFC24 H21 Cl N2 OP 1 21/n 17.529; 8.7083; 29.448
90; 90; 90
1930.8Wang, Kezhou; Wang, Linqing; Liu, Xihong; Li, Dan; Zhu, Haiyong; Wang, Pengxin; Liu, Yuyang; Yang, Dongxu; Wang, Rui
Development of Biligands Magnesium Catalysis in Asymmetric Conjugate Reactions of C3-Pyrrolyl-Oxindoles.
Organic letters, 2017, 19, 4351-4354
1547083 CIFC17 H14 N2 O3P 1 21/n 15.5929; 11.3901; 22.1102
90; 93.835; 90
1405.35Shi, Pengfei; Wang, Lili; Guo, Shan; Chen, Kehao; Wang, Jie; Zhu, Jin
A C-H Activation-Based Strategy for N-Amino Azaheterocycle Synthesis.
Organic letters, 2017, 19, 4359-4362
1547084 CIFC13 H13 F3 N2 O2P -17.8773; 7.9192; 10.3429
87.686; 89.889; 85.028
642.26Shi, Pengfei; Wang, Lili; Guo, Shan; Chen, Kehao; Wang, Jie; Zhu, Jin
A C-H Activation-Based Strategy for N-Amino Azaheterocycle Synthesis.
Organic letters, 2017, 19, 4359-4362
1547085 CIFC52 H50 N2 O4 SiP c a 2120.8; 13.066; 16.207
90; 90; 90
4404.6Ma, Zetong; Xiao, Chengyi; Liu, Chunming; Meng, Dong; Jiang, Wei; Wang, Zhaohui
Palladium-Catalyzed Si-C Bond Formation toward Sila-Annulated Perylene Diimides.
Organic letters, 2017, 19, 4331-4334
1547086 CIFC40 H28 F14 N2 O4 Si2C 1 2/c 128.533; 6.3805; 21.155
90; 99.386; 90
3799.8Ma, Zetong; Xiao, Chengyi; Liu, Chunming; Meng, Dong; Jiang, Wei; Wang, Zhaohui
Palladium-Catalyzed Si-C Bond Formation toward Sila-Annulated Perylene Diimides.
Organic letters, 2017, 19, 4331-4334
1547087 CIFC36 H20 F14 N2 O4 SiP 1 21/c 116.491; 16.508; 13.19
90; 102.583; 90
3505Ma, Zetong; Xiao, Chengyi; Liu, Chunming; Meng, Dong; Jiang, Wei; Wang, Zhaohui
Palladium-Catalyzed Si-C Bond Formation toward Sila-Annulated Perylene Diimides.
Organic letters, 2017, 19, 4331-4334
1547088 CIFC70 H74 N2 O4 Si2P -112.123; 15.118; 18.055
67.88; 82.56; 70.67
2892.6Ma, Zetong; Xiao, Chengyi; Liu, Chunming; Meng, Dong; Jiang, Wei; Wang, Zhaohui
Palladium-Catalyzed Si-C Bond Formation toward Sila-Annulated Perylene Diimides.
Organic letters, 2017, 19, 4331-4334
1547089 CIFC19 H25 N3 O7 SP 15.8603; 8.7507; 19.9834
95.115; 90.454; 97.456
1011.87Prasad, Sure Siva; Senthilkumar, Soundararasu; Srivastava, Akriti; Baskaran, Sundarababu
Iminosugar C-Nitromethyl Glycosides and Divergent Synthesis of Bicyclic Iminosugars.
Organic letters, 2017, 19, 4403-4406
1547090 CIFC10 H10 Br Mn N2 O3P -16.761; 7.2814; 13.336
78.215; 85.488; 72.757
613.7Bruneau-Voisine, Antoine; Wang, Ding; Dorcet, Vincent; Roisnel, Thierry; Darcel, Christophe; Sortais, Jean-Baptiste
Transfer Hydrogenation of Carbonyl Derivatives Catalyzed by an Inexpensive Phosphine-Free Manganese Precatalyst.
Organic letters, 2017, 19, 3656-3659
1547091 CIFC25 H21 N O2P 1 21 112.2212; 13.1633; 12.165
90; 89.91; 90
1957Chatterjee, Sourav; Hintermann, Lukas; Mandal, Madhumita; Achari, Anushree; Gupta, Sreya; Jaisankar, Parasuraman
Fiaud's Acid: A Brønsted Acid Catalyst for Enantioselective Friedel-Crafts Alkylation of Indoles with 2-Alkene-1,4-diones.
Organic letters, 2017, 19, 3426-3429
1547092 CIFC25 H25 Br O7P 21 21 216.5332; 8.086; 44.285
90; 90; 90
2339.5Gao, Ya-Ru; Wang, Da-Yu; Wang, Yong-Qiang
Asymmetric Syntheses of Amaryllidaceae Alkaloids (-)-Crinane and (+)-4a-Dehydroxycrinamabine.
Organic letters, 2017, 19, 3516-3519
1547093 CIFC21 H22 N2 O7P 17.5; 10.984; 12.966
79.535; 87.356; 75.611
1017.4Read, Jacquelyne A.; Yang, Yingying; Woerpel, K. A.
Additions of Organomagnesium Halides to α-Alkoxy Ketones: Revision of the Chelation-Control Model.
Organic letters, 2017, 19, 3346-3349
1547094 CIFC36 H48 B N O5 SiP -17.2437; 15.956; 15.979
93.5; 95.99; 100.034
1802.8Xiong, Meijun; Xie, Xin; Liu, Yuanhong
Copper-Catalyzed Borylative Cyclization of in Situ Generated o-Allenylaryl Nitriles with Bis(pinacolato)diboron.
Organic letters, 2017, 19, 3398-3401
1547095 CIFC14 H10 I NP 1 21/c 110.89; 12.636; 8.646
90; 94.343; 90
1186.3Sakata, Naoki; Sasakura, Kohei; Matsushita, Gaku; Okamoto, Kazuhiro; Ohe, Kouichi
Copper-Catalyzed Regio- and Stereoselective Iodocyanation and Dicyanation of Alkynes with Cyanogen Iodide.
Organic letters, 2017, 19, 3422-3425
1547096 CIFC21 H17 N3 O3P 42/n20.109; 20.109; 9.5683
90; 90; 90
3869.2Li, Xuanxuan; Fang, Xinxin; Zhuang, Shengyi; Liu, Ping; Sun, Peipei
Photoredox Catalysis: Construction of Polyheterocycles via Alkoxycarbonylation/Addition/Cyclization Sequence.
Organic letters, 2017, 19, 3580-3583
1547097 CIFC17 H16 O2P 1 21/n 112.241; 5.7694; 18.543
90; 101.136; 90
1284.9Chaudhari, Moreshwar B.; Sutar, Yogesh; Malpathak, Shreyas; Hazra, Anirban; Gnanaprakasam, Boopathy
Transition-Metal-Free C-H Hydroxylation of Carbonyl Compounds.
Organic letters, 2017, 19, 3628-3631
1547098 CIFC32 H25 F3 N2 O2C 1 2/c 127.948; 10.781; 21.83
90; 124.025; 90
5451.4Qin, Shuang; Zheng, Yan; Zhang, Fa-Guang; Ma, Jun-An
One-Pot Cascade Transformations of Zinc Trifluorodiazoethylide and α,β-Unsaturated Enones: Access to Trifluoromethylated Polycyclic Pyrazolines.
Organic letters, 2017, 19, 3406-3409
1547099 CIFC21 H21 N OP 1 21/n 111.6546; 6.183; 23.033
90; 100.63; 90
1631.3Daniel, Paige E.; Weber, Alexandria E.; Malcolmson, Steven J.
Umpolung Synthesis of 1,3-Amino Alcohols: Stereoselective Addition of 2-Azaallyl Anions to Epoxides.
Organic letters, 2017, 19, 3490-3493
1547100 CIFC25 H30 N2 O4 SF d d 216.0693; 54.037; 10.9426
90; 90; 90
9501.9Zhao, Quan-Qing; Chen, Jun; Yan, Dong-Mei; Chen, Jia-Rong; Xiao, Wen-Jing
Photocatalytic Hydrazonyl Radical-Mediated Radical Cyclization/Allylation Cascade: Synthesis of Dihydropyrazoles and Tetrahydropyridazines.
Organic letters, 2017, 19, 3620-3623
1547101 CIFC11 H11 Cl O3P 21 21 216.1106; 9.3146; 18.416
90; 90; 90
1048.2Huang, Wei-Lun; Raja, Arun; Hong, Bor-Cherng; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Acetalization-Reduction-Nef Reaction for a One-Pot Entry to the Functionalized Aflatoxin System. Total Synthesis of (-)- Dihydroaflatoxin D2 and (-)- and (+)-Microminutinin.
Organic letters, 2017, 19, 3494-3497
1547102 CIFC19 H27 B I N O5P 21 21 219.8874; 11.4556; 37.795
90; 90; 90
4280.9Chen, Lili; Zou, Xiaoliang; Zhao, Haonan; Xu, Senmiao
Copper-Catalyzed Asymmetric Protoboration of β-Amidoacrylonitriles and β-Amidoacrylate Esters: An Efficient Approach to Functionalized Chiral α-Amino Boronate Esters.
Organic letters, 2017, 19, 3676-3679
1547103 CIFC18 H24 B N3 O2P -17.742; 10.5041; 11.1422
97.83; 94.56; 103.792
865.86Allen, Thomas H.; Kawamoto, Takuji; Gardner, Sean; Geib, Steven J.; Curran, Dennis P.
N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters.
Organic letters, 2017, 19, 3680-3683
1547104 CIFC19 H26 Cl O3.5C 1 2 118.6435; 6.1999; 15.8122
90; 90.137; 90
1827.69Luo, Weiwei; Lin, Lili; Zhang, Yu; Liu, Xiaohua; Feng, Xiaoming
Construction of Distant Stereocenters by Enantioselective Desymmetrizing Carbonyl-Ene Reaction.
Organic letters, 2017, 19, 3374-3377
1547105 CIFC24 H26 N2 O2 SP 21 21 219.3681; 9.682; 23.6969
90; 90; 90
2149.35Tian, Hua; Zhang, Pengxiang; Peng, Fei; Yang, Haijun; Fu, Hua
Chiral Cyclic Ligand-Enabled Iridium-Catalyzed Asymmetric Arylation of Unactivated Racemic Allylic Alcohols with Anilines.
Organic letters, 2017, 19, 3775-3778
1547106 CIFC26 H25 N O5 S2P 1 21/c 110.796; 11.834; 19.55
90; 97.95; 90
2473.7Sun, Jiaqiong; Zheng, Guangfan; Zhang, Qiao; Wang, Yimin; Yang, Shengbiao; Zhang, Qian; Li, Yan; Zhang, Qian
Copper-Catalyzed Imidovinylation of Alkynes via 1,3-Vinyl Migration.
Organic letters, 2017, 19, 3767-3770
1547107 CIFC20 H30 O5P 1 21 17.805; 11.0195; 21.568
90; 93.907; 90
1850.69Zhou, Junfei; Zhan, Guanqun; Zhang, Hanqi; Zhang, Qihua; Li, Ying; Xue, Yongbo; Yao, Guangmin
Rhodomollanol A, a Highly Oxygenated Diterpenoid with a 5/7/5/5 Tetracyclic Carbon Skeleton from the Leaves of Rhododendron molle.
Organic letters, 2017, 19, 3935-3938
1547108 CIFC23 H22 N4 O5 S2P 1 21/n 18.6611; 11.0315; 24.1732
90; 98.964; 90
2281.4Zheng, Xuchun; Wan, Yanjun; Ling, Fei; Ma, Cheng
Copper-Catalyzed Tandem Reaction of Terminal Alkynes and Sulfonyl Azides for the Assembly of Substituted Aminotriazoles.
Organic letters, 2017, 19, 3859-3862
1547109 CIFC17 H18 N4 O2 SP -19.7392; 10.1552; 10.2805
100.715; 102.225; 114.844
857.35Zheng, Xuchun; Wan, Yanjun; Ling, Fei; Ma, Cheng
Copper-Catalyzed Tandem Reaction of Terminal Alkynes and Sulfonyl Azides for the Assembly of Substituted Aminotriazoles.
Organic letters, 2017, 19, 3859-3862
1547110 CIFC23 H31 N O5P 1 21 110.3276; 8.421; 13.1353
90; 95.4153; 90
1137.26Mallik, Sumitava; Bhajammanavar, Vinod; Ramakrishna, Isai; Baidya, Mahiuddin
Cross-Aldol Reaction of Activated Carbonyls with Nitrosocarbonyl Intermediates: Stereoselective Synthesis toward α-Hydroxy-β-amino Esters and Amides.
Organic letters, 2017, 19, 3843-3846
1547111 CIFC34 H31 Br N2 O4P -19.9071; 12.2529; 13.6988
98.655; 110.948; 98.93
1495.45Kang, Zhenghui; Zhang, Dan; Hu, Wenhao
Regio- and Diastereoselective Three-Component Reactions via Trapping of Ammonium Ylides with N-Alkylquinolinium Salts: Synthesis of Multisubstituted Tetra- and Dihydroquinoline Derivatives.
Organic letters, 2017, 19, 3783-3786
1547112 CIFC34 H31 Br N2 O4P 1 2/c 112.1984; 10.6577; 23.0168
90; 102.007; 90
2926.88Kang, Zhenghui; Zhang, Dan; Hu, Wenhao
Regio- and Diastereoselective Three-Component Reactions via Trapping of Ammonium Ylides with N-Alkylquinolinium Salts: Synthesis of Multisubstituted Tetra- and Dihydroquinoline Derivatives.
Organic letters, 2017, 19, 3783-3786
1547113 CIFC50 H60 O20P -111.9227; 12.587; 17.743
104.756; 102.056; 106.028
2360.5Zafrani, Yossi; Cohen, Yoram
Calix[4, 5]tetrolarenes: A New Family of Macrocycles.
Organic letters, 2017, 19, 3719-3722
1547114 CIFC18 H16 N2 OP 1 21/c 112.1454; 7.1266; 15.9769
90; 97.206; 90
1371.96Di Mauro, Giovanni; Maryasin, Boris; Kaiser, Daniel; Shaaban, Saad; González, Leticia; Maulide, Nuno
Mechanistic Pathways in Amide Activation: Flexible Synthesis of Oxazoles and Imidazoles.
Organic letters, 2017, 19, 3815-3818
1547115 CIFC30 H36 O7P 21 21 218.2009; 17.7433; 18.2546
90; 90; 90
2656.2Wang, Li; Yang, Jing; Kong, Ling-Mei; Deng, Jun; Xiong, Zijun; Huang, Jianping; Luo, Jianying; Yan, Yijun; Hu, Yikao; Li, Xiao-Nian; Li, Yan; Zhao, Yong; Huang, Sheng-Xiong
Natural and Semisynthetic Tigliane Diterpenoids with New Carbon Skeletons from Euphorbia dracunculoides as a Wnt Signaling Pathway Inhibitor.
Organic letters, 2017, 19, 3911-3914
1547116 CIFC19 H20 Cl N3 OP -19.1962; 10.3604; 10.8251
66.281; 78.926; 66.979
868.32Mondal, Susmita; Samanta, Sadhanendu; Singsardar, Mukta; Hajra, Alakananda
Aminomethylation of Imidazoheterocycles with Morpholine.
Organic letters, 2017, 19, 3751-3754
1547117 CIFC32 H35 Br Co F6 N O SbP 1 21/c 17.7258; 26.4404; 15.2454
90; 95.607; 90
3099.3Sen, Malay; Dahiya, Pardeep; Premkumar, J. Richard; Sundararaju, Basker
Dehydrative Cp*Co(III)-Catalyzed C-H Bond Allenylation.
Organic letters, 2017, 19, 3699-3702
1547118 CIFC25 H21 N2 O3P n a 219.6628; 18.241; 11.829
90; 90; 90
2085Singh, Ravi P.; Das, Jayanta; Yousufuddin, Muhammed; Gout, Delphine; Lovely, Carl J.
Tandem Oxidative Dearomatizing Spirocyclizations of Propargyl Guanidines and Ureas.
Organic letters, 2017, 19, 4110-4113
1547119 CIFC17 H10 O2P -17.9901; 9.9985; 16.101
101.591; 98.611; 107.446
1171.4Chen, Renjie; Cui, Sunliang
Rh(III)-Catalyzed C-H Activation/Cyclization of Benzamides and Diazonaphthalen-2(1H)-ones for Synthesis of Lactones.
Organic letters, 2017, 19, 4002-4005
1547120 CIFC27 H33 N O5C 1 2/c 125.0398; 10.8136; 18.7266
90; 104.572; 90
4907.5Liao, Jia-Yu; Ni, Qijian; Zhao, Yu
Catalyst-Enabled Scaffold Diversity: Highly Chemo- and Stereoselective Synthesis of Tricyclic Ketals and Triarylmethanes.
Organic letters, 2017, 19, 4074-4077
1547121 CIFC9 H12 O3P 1 21/c 17.882; 9.3288; 11.9801
90; 105.794; 90
847.64Armaly, Ahlam M.; Bar, Sukanta; Schindler, Corinna S.
Aluminum Chloride-Mediated Dieckmann Cyclization for the Synthesis of Cyclic 2-Alkyl-1,3-alkanediones: One-Step Synthesis of the Chiloglottones.
Organic letters, 2017, 19, 3958-3961
1547122 CIFC23 H17 N3 O2P 1 21/n 111.4016; 7.4909; 21.112
90; 93.186; 90
1800.4Liu, Shuang-Liang; Li, Yang; Guo, Jun-Ru; Yang, Guang-Chao; Li, Xue-Hong; Gong, Jun-Fang; Song, Mao-Ping
An Approach to 3-(Indol-2-yl)succinimide Derivatives by Manganese-Catalyzed C-H Activation.
Organic letters, 2017, 19, 4042-4045
1547123 CIFC30 H32 N2 O4 SP -19.0918; 12.255; 12.832
74.988; 88.662; 88.721
1380.4Li, Tian-Ren; Lu, Liang-Qiu; Wang, Ya-Ni; Wang, Bao-Cheng; Xiao, Wen-Jing
Divergent Synthesis of Polycyclic Indolines: Copper-Catalyzed Cascade Reactions of Propargylic Carbamates and Indoles.
Organic letters, 2017, 19, 4098-4101
1547124 CIFC32 H23 Br2 N OP 1 21/c 17.7055; 25.8797; 13.0746
90; 107.697; 90
2483.9Huang, Kai; Sheng, Guorong; Lu, Ping; Wang, Yanguang
BF3-Promoted Divergent Reactions between Tryptophols and Propargylic Alcohols.
Organic letters, 2017, 19, 4114-4117
1547125 CIFC26 H26 N4 O5P 17.2089; 8.081; 20.594
81.103; 84.522; 84.478
1175.8Kadam, Abhishek A.; Ellern, Arkady; Stanley, Levi M.
Enantioselective, Palladium-Catalyzed Conjugate Additions of Arylboronic Acids to Form Bis-benzylic Quaternary Stereocenters.
Organic letters, 2017, 19, 4062-4065
1547126 CIFC18 H15 Cl N2 OP 1 21/c 111.603; 7.704; 16.6899
90; 95.102; 90
1485.99Li, Bo; Fang, Sheng-Long; Huang, Dan-Ying; Shi, Bing-Feng
Ru-Catalyzed Meta-C-H Benzylation of Arenes with Toluene Derivatives.
Organic letters, 2017, 19, 3950-3953
1547127 CIFC64 H41 F12 N7 O10P 41 2 214.396; 14.396; 68.44
90; 90; 90
14184Ema, Tadashi; Yokoyama, Maki; Watanabe, Sagiri; Sasaki, Sota; Ota, Hiromi; Takaishi, Kazuto
Chiral Macrocyclic Organocatalysts for Kinetic Resolution of Disubstituted Epoxides with Carbon Dioxide.
Organic letters, 2017, 19, 4070-4073
1547130 CIFC24 H23 Br N2 O2 SP 1 21/c 113.366; 15.726; 11.497
90; 110.678; 90
2260.9Yang, Meng-Nan; Yan, Dong-Mei; Zhao, Quan-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
Synthesis of Dihydropyrazoles via Ligand-Free Pd-Catalyzed Alkene Aminoarylation of Unsaturated Hydrazones with Diaryliodonium Salts.
Organic letters, 2017, 19, 5208-5211
1547131 CIFC23 H22 N2 O2 SC 1 2/c 125.609; 10.536; 19.793
90; 130.31; 90
4072.4Yang, Meng-Nan; Yan, Dong-Mei; Zhao, Quan-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
Synthesis of Dihydropyrazoles via Ligand-Free Pd-Catalyzed Alkene Aminoarylation of Unsaturated Hydrazones with Diaryliodonium Salts.
Organic letters, 2017, 19, 5208-5211
1547132 CIFC17 H18 N2 O2 SP -19.2443; 9.2239; 11.5114
99.4294; 99.6133; 116.121
837.12Yang, Meng-Nan; Yan, Dong-Mei; Zhao, Quan-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
Synthesis of Dihydropyrazoles via Ligand-Free Pd-Catalyzed Alkene Aminoarylation of Unsaturated Hydrazones with Diaryliodonium Salts.
Organic letters, 2017, 19, 5208-5211
1547133 CIFC17 H20 Br N O4P -16.3863; 12.2125; 12.3641
100.937; 101.585; 103.902
887.81Jurberg, Igor D.; Davies, Huw M. L.
Rhodium- and Non-Metal-Catalyzed Approaches for the Conversion of Isoxazol-5-ones to 2,3-Dihydro-6H-1,3-oxazin-6-ones.
Organic letters, 2017, 19, 5158-5161
1547159 CIFC39 H40 N4 O10P 1 21 112.6396; 20.1301; 14.184
90; 91.5813; 90
3607.55Zhang, Wei; Xu, Wei; Wang, Gui-Yang; Gong, Xue-Ying; Li, Ni-Ping; Wang, Lei; Ye, Wen-Cai
Gelsekoumidines A and B: Two Pairs of Atropisomeric Bisindole Alkaloids from the Roots of Gelsemium elegans.
Organic letters, 2017, 19, 5194-5197
1547160 CIFC64 H60 O8P 1 21/c 115.703; 24.65; 14.556
90; 103.451; 90
5479.8Li, Youpeng; Hong, Youhua; Guo, Jing; Huang, Xiaobo; Wei, Haipeng; Zhou, Jun; Qiu, Tiancheng; Wu, Jishan; Zeng, Zebing
Bay- and Ortho-Octasubstituted Perylenes.
Organic letters, 2017, 19, 5094-5097
1547161 CIFC40 H40 N4 O4P b c a14.514; 10.865; 44.055
90; 90; 90
6947Li, Youpeng; Hong, Youhua; Guo, Jing; Huang, Xiaobo; Wei, Haipeng; Zhou, Jun; Qiu, Tiancheng; Wu, Jishan; Zeng, Zebing
Bay- and Ortho-Octasubstituted Perylenes.
Organic letters, 2017, 19, 5094-5097
1547162 CIFC40 H52 O8P b c a12.6363; 23.284; 25.125
90; 90; 90
7392.4Li, Youpeng; Hong, Youhua; Guo, Jing; Huang, Xiaobo; Wei, Haipeng; Zhou, Jun; Qiu, Tiancheng; Wu, Jishan; Zeng, Zebing
Bay- and Ortho-Octasubstituted Perylenes.
Organic letters, 2017, 19, 5094-5097
1547163 CIFC21 H17 I N2 O3P 21 21 217.6528; 12.1548; 21.7284
90; 90; 90
2021.14Liang, Lei; Xie, Ming-Sheng; Qin, Tao; Zhu, Man; Qu, Gui-Rong; Guo, Hai-Ming
Regio- and Enantioselective Synthesis of Chiral Pyrimidine Acyclic Nucleosides via Rhodium-Catalyzed Asymmetric Allylation of Pyrimidines.
Organic letters, 2017, 19, 5212-5215
1547164 CIFC21 H20 F3 N O9C 1 2 165.689; 4.6345; 21.077
90; 100.837; 90
6302.2Probst, Nicolas; Grelier, Gwendal; Ghermani, NourEddine; Gandon, Vincent; Alami, Mouâd; Messaoudi, Samir
Intramolecular Pd-Catalyzed Anomeric C(sp(3))-H Activation of Glycosyl Carboxamides.
Organic letters, 2017, 19, 5038-5041
1547165 CIFC25 H19.5 F3 N2 O1.25P -110.3304; 17.89; 23.784
96.034; 99.172; 99.186
4245.1Gao, Yuelei; Hu, Zhongyan; Dong, Jinhuan; Liu, Jun; Xu, Xianxiu
Chemoselective Double Annulation of Two Different Isocyanides: Rapid Access to Trifluoromethylated Indole-Fused Heterocycles.
Organic letters, 2017, 19, 5292-5295
1547166 CIFC46 H31 Cl4 N O2P b c n24.3391; 8.299; 35.4906
90; 90; 90
7168.8Shoyama, Kazutaka; Schmidt, David; Mahl, Magnus; Würthner, Frank
Electron-Poor Bowl-Shaped Polycyclic Aromatic Dicarboximides: Synthesis, Crystal Structures, and Optical and Redox Properties.
Organic letters, 2017, 19, 5328-5331
1547167 CIFC82 H64 N2 O4P 1 21/n 113.408; 14.6595; 31.3393
90; 98.0086; 90
6099.8Shoyama, Kazutaka; Schmidt, David; Mahl, Magnus; Würthner, Frank
Electron-Poor Bowl-Shaped Polycyclic Aromatic Dicarboximides: Synthesis, Crystal Structures, and Optical and Redox Properties.
Organic letters, 2017, 19, 5328-5331
1547168 CIFC21 H25 N O3 SP 1 21/c 112.5138; 17.6266; 19.7375
90; 117.443; 90
3863.7Kazak, Mihail; Priede, Martins; Shubin, Kirill; Bartrum, Hannah E.; Poisson, Jean-François; Suna, Edgars
Stereodivergent Synthesis of Pseudotabersonine Alkaloids.
Organic letters, 2017, 19, 5356-5359
1547169 CIFC19 H27 N O2 SP 21 21 217.4989; 11.9755; 20.6566
90; 90; 90
1855.03Kazak, Mihail; Priede, Martins; Shubin, Kirill; Bartrum, Hannah E.; Poisson, Jean-François; Suna, Edgars
Stereodivergent Synthesis of Pseudotabersonine Alkaloids.
Organic letters, 2017, 19, 5356-5359
1547170 CIFC42 H34P -17.1561; 8.0619; 12.865
87.837; 88.161; 75.494
717.84Barker, Joshua E.; Frederickson, Conerd K.; Jones, Michael H.; Zakharov, Lev N.; Haley, Michael M.
Synthesis and Properties of Quinoidal Fluorenofluorenes.
Organic letters, 2017, 19, 5312-5315
1547176 CIFC17 H13 Br N2 O2P 4314.4914; 14.4914; 14.4935
90; 90; 90
3043.64Meninno, Sara; Roselli, Angelo; Capobianco, Amedeo; Overgaard, Jacob; Lattanzi, Alessandra
Diastereodivergent and Enantioselective Access to Spiroepoxides via Organocatalytic Epoxidation of Unsaturated Pyrazolones.
Organic letters, 2017, 19, 5030-5033
1547177 CIFC17 H13 Cl N2 O2P 21 21 218.3966; 10.4923; 16.3473
90; 90; 90
1440.19Meninno, Sara; Roselli, Angelo; Capobianco, Amedeo; Overgaard, Jacob; Lattanzi, Alessandra
Diastereodivergent and Enantioselective Access to Spiroepoxides via Organocatalytic Epoxidation of Unsaturated Pyrazolones.
Organic letters, 2017, 19, 5030-5033
1547178 CIFC77 H15 N O2 S3P 1 21/n 19.9333; 32.2929; 28.6843
90; 96.813; 90
9136.2Jiang, Sheng-Peng; Zhang, Mengmeng; Wang, Cheng-Yu; Yang, Shangfeng; Wang, Guan-Wu
Cascade Radical Reaction of N-Sulfonyl-2-allylanilines with [60]Fullerene: Synthesis and Functionalization of (2-Indolinyl)methylated Hydrofullerenes.
Organic letters, 2017, 19, 5110-5113
1547179 CIFC17 H14 N2 OP 1 21/a 114.4154; 6.024; 15.0935
90; 94.616; 90
1306.44Sato, Takenari; Yoshida, Takumi; Al Mamari, Hamad H.; Ilies, Laurean; Nakamura, Eiichi
Manganese-Catalyzed Directed Methylation of C(sp(2))-H Bonds at 25 °C with High Catalytic Turnover.
Organic letters, 2017, 19, 5458-5461
1547195 CIFC14 H16 O4P b c a11.3435; 12.4428; 18.028
90; 90; 90
2544.6Smith, Brandon R.; Njardarson, Jon T.
Double-Diels-Alder Approach to Maoecrystal V. Unexpected C-C Bond-Forming Fragmentations of the [2.2.2]-Bicyclic Core.
Organic letters, 2017, 19, 5316-5319
1547196 CIFC20 H22 O5P 1 21/n 112.3331; 12.5411; 12.506
90; 117.489; 90
1715.93Smith, Brandon R.; Njardarson, Jon T.
Double-Diels-Alder Approach to Maoecrystal V. Unexpected C-C Bond-Forming Fragmentations of the [2.2.2]-Bicyclic Core.
Organic letters, 2017, 19, 5316-5319
1547197 CIFC22 H22 N2 O6P 1 21 16.105; 17.278; 9.698
90; 97.095; 90
1015.1Lin, Zhichen; Hu, Zhongyan; Zhang, Xin; Dong, Jinhuan; Liu, Jian-Biao; Chen, De-Zhan; Xu, Xianxiu
Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction.
Organic letters, 2017, 19, 5284-5287
1547221 CIFC21 H24 O10P -17.1541; 12.2169; 12.5923
64.384; 84.733; 89.351
987.72Wang, Rurun; Seyedsayamdost, Mohammad R.
Roseochelin B, an Algaecidal Natural Product Synthesized by the Roseobacter Phaeobacter inhibens in Response to Algal Sinapic Acid.
Organic letters, 2017, 19, 5138-5141
1547222 CIFC22 H24 O9 SP -18.4319; 11.7976; 13.0028
89.9418; 106.386; 106.877
1182.87Wang, Rurun; Seyedsayamdost, Mohammad R.
Roseochelin B, an Algaecidal Natural Product Synthesized by the Roseobacter Phaeobacter inhibens in Response to Algal Sinapic Acid.
Organic letters, 2017, 19, 5138-5141
1547223 CIFC22 H20 F N OP 1 21/n 113.4005; 9.5236; 14.6548
90; 105.033; 90
1806.25Zheng, Lewei; Gao, Fei; Yang, Chao; Gao, Guo-Lin; Zhao, Yating; Gao, Yuan; Xia, Wujiong
Visible-Light-Mediated Anti-Regioselective Nitrone 1,3-Dipolar Cycloaddition Reaction and Synthesis of Bisindolylmethanes.
Organic letters, 2017, 19, 5086-5089
1547224 CIFC22 H21 N OP -18.4694; 9.9145; 11.0455
104.21; 93.496; 100.126
879.82Zheng, Lewei; Gao, Fei; Yang, Chao; Gao, Guo-Lin; Zhao, Yating; Gao, Yuan; Xia, Wujiong
Visible-Light-Mediated Anti-Regioselective Nitrone 1,3-Dipolar Cycloaddition Reaction and Synthesis of Bisindolylmethanes.
Organic letters, 2017, 19, 5086-5089
1547225 CIFC23 H19 N OP 1 21/c 113.668; 12.191; 11.563
90; 112.665; 90
1777.9Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547226 CIFC24 H21 N OP 1 21/c 19.3245; 19.8436; 9.8852
90; 97.067; 90
1815.18Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547227 CIFC27 H21 N OP 1 21/n 19.4551; 11.3229; 18.946
90; 97.519; 90
2010.9Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547228 CIFC23 H18 Cl N OP 1 21/c 114.8; 12.024; 11.523
90; 112.388; 90
1896Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547229 CIFC23 H18 F N OI b a 217.5173; 11.7477; 17.1922
90; 90; 90
3537.9Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547230 CIFC19 H19 N OP 18.4979; 9.606; 9.7613
90.716; 105.714; 100.679
752.1Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547231 CIFC24 H21 N O2C 1 2/c 125.773; 12.89; 11.497
90; 91.868; 90
3817.4Hu, Yue; Huang, Hanmin
Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.
Organic letters, 2017, 19, 5070-5073
1547234 CIFC23 H21 F3 N2 O SP 1 21/n 117.843; 22.6128; 23.019
90; 104.466; 90
8993.3Zhao, Qun; Poisson, Thomas; Pannecoucke, Xavier; Bouillon, Jean-Philippe; Besset, Tatiana
Pd-Catalyzed Diastereoselective Trifluoromethylthiolation of Functionalized Acrylamides.
Organic letters, 2017, 19, 5106-5109
1547235 CIFC15 H12 O3P 1 21/c 18.0887; 6.4489; 22.5011
90; 93.799; 90
1171.15Ogiwara, Yohei; Sato, Kazuya; Sakai, Norio
Palladium-Catalyzed Cyclization of Alkynoic Acids To Form Vinyl Dioxanones Bearing a Quaternary Allylic Carbon.
Organic letters, 2017, 19, 5296-5299
1547236 CIFC18 H18 Cl Co F N O2P b c a13.6337; 14.573; 17.0961
90; 90; 90
3396.7Yu, Xiaolong; Chen, Kehao; Guo, Shan; Shi, Pengfei; Song, Chao; Zhu, Jin
Direct Access to Cobaltacycles via C-H Activation: N-Chloroamide-Enabled Room-Temperature Synthesis of Heterocycles.
Organic letters, 2017, 19, 5348-5351
1547237 CIFC19 H22 Br Cl Co N O3P 1 21/c 18.3729; 18.1458; 14.1298
90; 113.125; 90
1974.29Yu, Xiaolong; Chen, Kehao; Guo, Shan; Shi, Pengfei; Song, Chao; Zhu, Jin
Direct Access to Cobaltacycles via C-H Activation: N-Chloroamide-Enabled Room-Temperature Synthesis of Heterocycles.
Organic letters, 2017, 19, 5348-5351
1547238 CIFC29 H16 S2P b c a15.2176; 8.3864; 32.8506
90; 90; 90
4192.4Takase, Ko; Noguchi, Keiichi; Nakano, Koji
Circularly Polarized Luminescence from Chiral Spiro Molecules: Synthesis and Optical Properties of 10,10'-Spirobi(indeno[1,2-b][1]benzothiophene) Derivatives.
Organic letters, 2017, 19, 5082-5085
1547239 CIFC31 H18 Cl6 O4 S2P 1 2/n 112.2019; 15.4584; 16.691
90; 94.737; 90
3137.53Takase, Ko; Noguchi, Keiichi; Nakano, Koji
Circularly Polarized Luminescence from Chiral Spiro Molecules: Synthesis and Optical Properties of 10,10'-Spirobi(indeno[1,2-b][1]benzothiophene) Derivatives.
Organic letters, 2017, 19, 5082-5085
1547240 CIFC13 H14 F N OP c a 2111.246; 17.285; 11.864
90; 90; 90
2306.2Han, Yong-Chao; Zhang, Yan-Dong; Jia, Qun; Cui, Jian; Zhang, Chi
Hypervalent-Iodine-Mediated Ring-Contraction Monofluorination Affording Monofluorinated Five-Membered Ring-Fused Oxazolines.
Organic letters, 2017, 19, 5300-5303
1547241 CIFC15 H18 F N OP 1 21/n 114.352; 8.032; 22.473
90; 95.996; 90
2576.4Han, Yong-Chao; Zhang, Yan-Dong; Jia, Qun; Cui, Jian; Zhang, Chi
Hypervalent-Iodine-Mediated Ring-Contraction Monofluorination Affording Monofluorinated Five-Membered Ring-Fused Oxazolines.
Organic letters, 2017, 19, 5300-5303
1547262 CIFC10 H19 B10 N O2P -17.708; 7.8648; 14.246
105.133; 90.39; 110.375
776.9Li, Chun-Xiao; Zhang, Hao-Yun; Wong, Tsz-Yung; Cao, Hou-Ji; Yan, Hong; Lu, Chang-Sheng
Pyridyl-Directed Cp*Rh(III)-Catalyzed B(3)-H Acyloxylation of o-Carborane.
Organic letters, 2017, 19, 5178-5181
1547263 CIFC17 H22 B10 N2 O2P -17.8102; 10.484; 14.408
101.922; 101.787; 102.815
1086.2Li, Chun-Xiao; Zhang, Hao-Yun; Wong, Tsz-Yung; Cao, Hou-Ji; Yan, Hong; Lu, Chang-Sheng
Pyridyl-Directed Cp*Rh(III)-Catalyzed B(3)-H Acyloxylation of o-Carborane.
Organic letters, 2017, 19, 5178-5181
1547264 CIFC18 H29 B10 N O4P -110.435; 10.813; 21.42
84.083; 81.585; 75.119
2305.3Li, Chun-Xiao; Zhang, Hao-Yun; Wong, Tsz-Yung; Cao, Hou-Ji; Yan, Hong; Lu, Chang-Sheng
Pyridyl-Directed Cp*Rh(III)-Catalyzed B(3)-H Acyloxylation of o-Carborane.
Organic letters, 2017, 19, 5178-5181
1547265 CIFC41 H42 N2 O2 SiP 1 21/n 112.4255; 15.7669; 17.6793
90; 102.091; 90
3386.7Williams, David R.; Bawel, Seth A.; Schaugaard, Richard N.
A Stereoselective Michael-Mannich Annelation Strategy for the Construction of Novel Tetrahydrocarbazoles.
Organic letters, 2017, 19, 5098-5101
1547295 CIFC12 H16 N2 O2P n a 2111.9025; 7.4111; 13.2657
90; 90; 90
1170.18Hao, Feiyue; Asahara, Haruyasu; Nishiwaki, Nagatoshi
Direct Aziridination of Nitroalkenes Affording N-Alkyl-C-nitroaziridines and the Subsequent Lewis Acid Mediated Isomerization to β-Nitroenamines.
Organic letters, 2017, 19, 5442-5445
1547296 CIFC17 H16 O2P 1 21/n 18.0103; 6.9176; 24.3023
90; 95.153; 90
1341.2Pan, Jin-Long; Chen, Chao; Ma, Zhi-Gang; Zhou, Jia; Wang, Li-Ren; Zhang, Shu-Yu
Stereoselective Synthesis of Z-Vinylsilanes via Palladium-Catalyzed Direct Intermolecular Silylation of C(sp(2))-H Bonds.
Organic letters, 2017, 19, 5216-5219
1547297 CIFC15 H18 N2 O SiP -17.9568; 13.6772; 14.6028
69.85; 87.671; 77.154
1453.44Pan, Jin-Long; Chen, Chao; Ma, Zhi-Gang; Zhou, Jia; Wang, Li-Ren; Zhang, Shu-Yu
Stereoselective Synthesis of Z-Vinylsilanes via Palladium-Catalyzed Direct Intermolecular Silylation of C(sp(2))-H Bonds.
Organic letters, 2017, 19, 5216-5219
1547298 CIFC21 H22 N2 O SiP 1 21/n 111.9573; 11.2275; 14.8598
90; 98.926; 90
1970.78Pan, Jin-Long; Chen, Chao; Ma, Zhi-Gang; Zhou, Jia; Wang, Li-Ren; Zhang, Shu-Yu
Stereoselective Synthesis of Z-Vinylsilanes via Palladium-Catalyzed Direct Intermolecular Silylation of C(sp(2))-H Bonds.
Organic letters, 2017, 19, 5216-5219
1547299 CIFC20 H13 F2 N3 O PdP 1 21/c 18.126; 20.9981; 11.7913
90; 120.091; 90
1740.81Pan, Jin-Long; Chen, Chao; Ma, Zhi-Gang; Zhou, Jia; Wang, Li-Ren; Zhang, Shu-Yu
Stereoselective Synthesis of Z-Vinylsilanes via Palladium-Catalyzed Direct Intermolecular Silylation of C(sp(2))-H Bonds.
Organic letters, 2017, 19, 5216-5219
1547300 CIFC18 H28 O3 SiP 1 21/c 119.273; 7.63; 12.384
90; 100.001; 90
1793.4Yang, Qianqian; Ma, Wenjing; Wang, Gaopeng; Bao, Wenli; Dong, Xiaoshu; Liang, Xuefeng; Zhu, Lizhi; Lee, Chi-Sing
Tunable Cyclization Strategy for the Synthesis of Zizaene-, allo-Cedrane-, seco-Kaurane-, and seco-Atesane-Type Skeletons.
Organic letters, 2017, 19, 5324-5327
1547301 CIFC21 H32 O3 SiP -17.3119; 11.552; 12.6325
104.854; 97.6124; 94.5246
1015.17Yang, Qianqian; Ma, Wenjing; Wang, Gaopeng; Bao, Wenli; Dong, Xiaoshu; Liang, Xuefeng; Zhu, Lizhi; Lee, Chi-Sing
Tunable Cyclization Strategy for the Synthesis of Zizaene-, allo-Cedrane-, seco-Kaurane-, and seco-Atesane-Type Skeletons.
Organic letters, 2017, 19, 5324-5327
1547302 CIFC14 H18 O2P -19.1835; 11.772; 11.8757
97.9911; 97.2935; 105.76
1205.18Yang, Qianqian; Ma, Wenjing; Wang, Gaopeng; Bao, Wenli; Dong, Xiaoshu; Liang, Xuefeng; Zhu, Lizhi; Lee, Chi-Sing
Tunable Cyclization Strategy for the Synthesis of Zizaene-, allo-Cedrane-, seco-Kaurane-, and seco-Atesane-Type Skeletons.
Organic letters, 2017, 19, 5324-5327
1547303 CIFC18 H28 O4 SiP 1 21/c 119.8426; 7.7701; 12.1168
90; 91.8138; 90
1867.22Yang, Qianqian; Ma, Wenjing; Wang, Gaopeng; Bao, Wenli; Dong, Xiaoshu; Liang, Xuefeng; Zhu, Lizhi; Lee, Chi-Sing
Tunable Cyclization Strategy for the Synthesis of Zizaene-, allo-Cedrane-, seco-Kaurane-, and seco-Atesane-Type Skeletons.
Organic letters, 2017, 19, 5324-5327
1547304 CIFC19 H30 O3 SiP 1 21/n 17.2951; 25.7751; 10.621
90; 95.7546; 90
1987.02Yang, Qianqian; Ma, Wenjing; Wang, Gaopeng; Bao, Wenli; Dong, Xiaoshu; Liang, Xuefeng; Zhu, Lizhi; Lee, Chi-Sing
Tunable Cyclization Strategy for the Synthesis of Zizaene-, allo-Cedrane-, seco-Kaurane-, and seco-Atesane-Type Skeletons.
Organic letters, 2017, 19, 5324-5327
1547305 CIFC25 H18 Cl F3 N2 O3 SP -18.9921; 14.991; 18.8794
70.038; 86.459; 82.52
2371.3Meng, Qiang; Chen, Fei; Yu, Wei; Han, Bing
Copper-Catalyzed Cascade Cyclization of 1,7-Enynes toward Trifluoromethyl-Substituted 1'H-Spiro[azirine-2,4'-quinolin]-2'(3'H)-ones.
Organic letters, 2017, 19, 5186-5189
1547310 CIFC28 H24 N4 O5 SeP -111.1051; 11.6556; 12.5568
65.997; 65.067; 67.782
1303.82Wu, Ping; Wu, Kaikai; Wang, Liandi; Yu, Zhengkun
Iron-Promoted Difunctionalization of Alkenes by Phenylselenylation/1,2-Aryl Migration.
Organic letters, 2017, 19, 5450-5453
1547311 CIFC28 H23 F N4 O5 SeP 1 21/c 113.0995; 13.8051; 15.6445
90; 112.12; 90
2620.9Wu, Ping; Wu, Kaikai; Wang, Liandi; Yu, Zhengkun
Iron-Promoted Difunctionalization of Alkenes by Phenylselenylation/1,2-Aryl Migration.
Organic letters, 2017, 19, 5450-5453
1547312 CIFC24 H19 N O2P -18.5275; 10.4444; 11.7063
71.7186; 77.0693; 66.7601
903.67Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547313 CIFC24 H19 N O2C 1 2/c 126.201; 9.1245; 16.2023
90; 108.289; 90
3677.8Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547314 CIFC31 H24 Cl3 N O2P -110.907; 11.8602; 12.5989
114.533; 105.84; 100.619
1341.35Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547315 CIFC30 H23 N O2P 1 21/n 19.0802; 9.9498; 24.9306
90; 98.8194; 90
2225.75Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547316 CIFC31 H23 N O4P 1 21/c 19.3618; 10.5515; 24.1467
90; 96.2562; 90
2371.03Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547317 CIFC27 H18 O2P -18.7392; 10.6106; 11.8953
73.1183; 78.1739; 66.4494
962.6Arunprasath, Dhanarajan; Devi Bala, Balasubramanian; Sekar, Govindasamy
Stereoselective Construction of α-Tetralone-Fused Spirooxindoles via Pd-Catalyzed Domino Carbene Migratory Insertion/Conjugate Addition Sequence.
Organic letters, 2017, 19, 5280-5283
1547318 CIFC20 H20 B N O4P 1 21/c 111.2003; 32.9681; 9.9704
90; 103.46; 90
3580.47Khanizeman, R. N.; Barde, E.; Bates, R. W.; Guérinot, A; Cossy, J.
Modular Access to Triarylethylene Units from Arylvinyl MIDA Boronates Using a Regioselective Heck Coupling.
Organic letters, 2017, 19, 5046-5049
1547357 CIFC25 H25 N2 O5 S2P 21 21 217.8958; 16.9193; 18.2874
90; 90; 90
2443.04Zhu, Shi-Ya; Zhang, Yuanzhen; Wang, Wei; Hui, Xin-Ping
Stereoselective Synthesis of Functionalized Tetrahydro-1H-1,2-diazepines by N-Heterocyclic Carbene-Catalyzed [3 + 4] Annulation.
Organic letters, 2017, 19, 5380-5383
1547358 CIFC23 H20 N2 O5P 21 21 211.5449; 34.1483; 4.9573
90; 90; 90
1954.36Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547359 CIFC23 H22 N2 O5P 21 21 211.3495; 36.3258; 4.7864
90; 90; 90
1973.34Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547360 CIFC15 H16 I N3 O7 SP 1 21 15.3844; 21.4986; 8.2956
90; 106.438; 90
921.02Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547361 CIFC27 H29 Cl2 I N2 O7C 1 2 122.1529; 9.8472; 15.6753
90; 121.483; 90
2916.1Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547362 CIFC24 H21 I3 N2 O5P 21 21 215.272; 14.4113; 33.766
90; 90; 90
2565.4Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547363 CIFC24 H24 N2 O5P 1 21 14.8466; 11.7928; 18.3146
90; 96.5347; 90
1039.97Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547364 CIFC25 H26 N2 O5P 1 21 18.9667; 7.6705; 16.1715
90; 92.338; 90
1111.33Atmuri, N. D. Prasad; Reilley, David J.; Lubell, William D.
Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7-9-Membered Lactams.
Organic letters, 2017, 19, 5066-5069
1547392 CIFC21 H32 O7P 21 21 2125.657; 6.1824; 12.8915
90; 90; 90
2044.9Zhou, Junfei; Sun, Na; Zhang, Hanqi; Zheng, Guijuan; Liu, Junjun; Yao, Guangmin
Rhodomollacetals A-C, PTP1B Inhibitory Diterpenoids with a 2,3:5,6-Di-seco-grayanane Skeleton from the Leaves of Rhododendron molle.
Organic letters, 2017, 19, 5352-5355
1547393 CIFC22 H34 O7P 1 21 112.1637; 6.9628; 13.0151
90; 104.05; 90
1069.32Zhou, Junfei; Sun, Na; Zhang, Hanqi; Zheng, Guijuan; Liu, Junjun; Yao, Guangmin
Rhodomollacetals A-C, PTP1B Inhibitory Diterpenoids with a 2,3:5,6-Di-seco-grayanane Skeleton from the Leaves of Rhododendron molle.
Organic letters, 2017, 19, 5352-5355
1547394 CIFC23 H27 F N2 O3P 21 21 2110.1934; 11.1437; 19.3947
90; 90; 90
2203.1Paladhi, Sushovan; Park, Sang Yeon; Yang, Jung Woon; Song, Choong Eui
Asymmetric Synthesis of α-Fluoro-β-Amino-oxindoles with Tetrasubstituted C-F Stereogenic Centers via Cooperative Cation-Binding Catalysis.
Organic letters, 2017, 19, 5336-5339
1547395 CIFC24 H18 F3 N O3 SP -18.0793; 9.9652; 13.6943
93.198; 105.789; 91.377
1058.42Liu, Bingxian; Hu, Panjie; Zhang, Ying; Li, Yunyun; Bai, Dachang; Li, Xingwei
Rh(III)-Catalyzed Diastereodivergent Spiroannulation of Cyclic Imines with Activated Alkenes.
Organic letters, 2017, 19, 5402-5405
1547396 CIFC24 H18 F3 N O3 SP 1 21/n 111.3446; 15.1444; 13.1535
90; 104.43; 90
2188.57Liu, Bingxian; Hu, Panjie; Zhang, Ying; Li, Yunyun; Bai, Dachang; Li, Xingwei
Rh(III)-Catalyzed Diastereodivergent Spiroannulation of Cyclic Imines with Activated Alkenes.
Organic letters, 2017, 19, 5402-5405
1547397 CIFC22 H17 N O3 SP 1 21/n 110.6461; 7.0696; 23.381
90; 95.897; 90
1750.4Liu, Bingxian; Hu, Panjie; Zhang, Ying; Li, Yunyun; Bai, Dachang; Li, Xingwei
Rh(III)-Catalyzed Diastereodivergent Spiroannulation of Cyclic Imines with Activated Alkenes.
Organic letters, 2017, 19, 5402-5405
1547398 CIFC23 H29 B O2P 21 21 216.8529; 11.4799; 26.6681
90; 90; 90
2098Chen, Chenhui; Shen, Xuzhong; Chen, Jianhui; Hong, Xin; Lu, Zhan
Iron-Catalyzed Hydroboration of Vinylcyclopropanes.
Organic letters, 2017, 19, 5422-5425
1547399 CIFC23 H18 Br N O3P -111.626; 13.194; 13.907
107.517; 91.291; 105.046
1952.8Zhang, Yuwen; Tong, Xiaofeng
Construction of Complex 1,3-Cyclohexadienes via Phosphine-Catalyzed (4 + 2) Annulations of δ-Acetoxy Allenoates and Ketones.
Organic letters, 2017, 19, 5462-5465
1547400 CIFC15 H20 O4P -17.3638; 8.8975; 11.801
68.539; 84.494; 78.362
704.6Zhang, Yuwen; Tong, Xiaofeng
Construction of Complex 1,3-Cyclohexadienes via Phosphine-Catalyzed (4 + 2) Annulations of δ-Acetoxy Allenoates and Ketones.
Organic letters, 2017, 19, 5462-5465
1547401 CIFC31 H23 Br2 N3 PdP -114.242; 15.1637; 15.545
61.832; 68.911; 89.354
2709.5Karthik, Shanmugam; Gandhi, Thirumanavelan
Palladium(II)/N-Heterocyclic Carbene-Catalyzed Direct C-H Acylation of Heteroarenes with N-Acylsaccharins.
Organic letters, 2017, 19, 5486-5489
1547454 CIFC25 H23 N O7 SP 21 21 219.60806; 11.4151; 20.1805
90; 90; 90
2213.34Takizawa, Shinobu; Sako, Makoto; Abozeid, Mohamed Ahmed; Kishi, Kenta; Wathsala, H. D. P.; Hirata, Shuichi; Murai, Kenichi; Fujioka, Hiromichi; Sasai, Hiroaki
Enantio- and Diastereoselective Betti/aza-Michael Sequence: Single Operated Preparation of Chiral 1,3-Disubstituted Isoindolines.
Organic letters, 2017, 19, 5426-5429
1547455 CIFC19 H16 F5 N O2P 1 21/c 17.5979; 16.309; 13.633
90; 91.809; 90
1688.5Zhang, Yunxiao; Yan, Weitao; Wang, Yukang; Weng, Zhiqiang
Copper-Catalyzed Synthesis of Indol-3-yl α-(Difluoromethyl)-α-(trifluoromethyl)carbinols: Construction of Difluoromethylated sp(3) Carbon Centers.
Organic letters, 2017, 19, 5478-5481
1547456 CIFC16 H15 F2 N3 OP 1 21/c 117.687; 10.7866; 7.8181
90; 92.685; 90
1489.9Zhang, Yunxiao; Yan, Weitao; Wang, Yukang; Weng, Zhiqiang
Copper-Catalyzed Synthesis of Indol-3-yl α-(Difluoromethyl)-α-(trifluoromethyl)carbinols: Construction of Difluoromethylated sp(3) Carbon Centers.
Organic letters, 2017, 19, 5478-5481
1547479 CIFC20 H24 O6P 21 21 217.3454; 10.9165; 22.3527
90; 90; 90
1792.37Shibuya, Grant M.; Enquist, John A., Jr.; Stoltz, Brian M.
Enantioselective Synthesis of the 5-6-7 Carbocyclic Core of the Gagunin Diterpenoids
Organic Letters, 2013, 15, 3480-3483
1547480 CIFC18 H22 O4P 21 21 217.1115; 8.2413; 26.074
90; 90; 90
1528.15Shibuya, Grant M.; Enquist, John A., Jr.; Stoltz, Brian M.
Enantioselective Synthesis of the 5-6-7 Carbocyclic Core of the Gagunin Diterpenoids
Organic Letters, 2013, 15, 3480-3483
1547489 CIFC15 H14 O4P 1 21/c 112.1023; 8.2733; 13.0573
90; 105.335; 90
1260.83Hsu, Day-Shin; Yeh, Jen-Yu; Cheng, Chiao-Yun
Total Synthesis of the Proposed Structure of (±)-Nidemone.
Organic letters, 2017, 19, 5549-5552
1547490 CIFC74 H122 Cl10 I4 P2 Pd2P -19.8299; 14.231; 17.386
102.214; 101.847; 98.259
2281.5Krause, Sarah B.; McAtee, Jesse R.; Yap, Glenn P. A.; Watson, Donald A.
A Bench-Stable, Single-Component Precatalyst for Silyl-Heck Reactions.
Organic letters, 2017, 19, 5641-5644
1547491 CIFC64 H102 P2 PdP 1 21/c 113.9909; 21.5456; 10.7208
90; 105.505; 90
3114.1Krause, Sarah B.; McAtee, Jesse R.; Yap, Glenn P. A.; Watson, Donald A.
A Bench-Stable, Single-Component Precatalyst for Silyl-Heck Reactions.
Organic letters, 2017, 19, 5641-5644
1547492 CIFC25 H29 N O5R 3 :H19.7299; 19.7299; 30.7413
90; 90; 120
10363.4Cui, Hui; Lin, Yun; Luo, Mingchu; Lu, Yongjun; Huang, Xishan; She, Zhigang
Diaporisoindoles A-C: Three Isoprenylisoindole Alkaloid Derivatives from the Mangrove Endophytic Fungus Diaporthe sp. SYSU-HQ3.
Organic letters, 2017, 19, 5621-5624
1547505 CIFC18 H17 N O3P 1 21/n 19.8851; 5.5559; 27.8824
90; 94.53; 90
1526.54Das, Tamal Kanti; Mondal, Santigopal; Gonnade, Rajesh G.; Biju, Akkattu T.
Base-Free and Catalyst-Free Synthesis of Functionalized Dihydrobenzoxazoles via Vinylogous Carbonate to Carbamate Rearrangement.
Organic letters, 2017, 19, 5597-5600
1547506 CIFC34 H33 N O7 SP n a 2121.688; 9.136; 30.698
90; 90; 90
6082.5Chen, Junlong; Huang, You
Phosphine-Catalyzed Sequential [4 + 3] Domino Annulation/Allylic Alkylation Reaction of MBH Carbonates: Efficient Construction of Seven-Membered Heterocycles.
Organic letters, 2017, 19, 5609-5612
1547507 CIFC12 H22 F3 N O3 SP 1 21/c 111.0625; 8.6759; 17.0878
90; 107.297; 90
1565.9Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547508 CIFC19 H34 F3 N3 O3 SP 1 21/c 113.4671; 8.2755; 20.6849
90; 100.909; 90
2263.6Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547509 CIFC23 H42 F3 N3 O3 SP 1 21/n 110.299; 8.3668; 29.872
90; 92.79; 90
2571Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547510 CIFC19 H33 F3 N3 O3 SP 1 21/c 113.4463; 8.2683; 20.7728
90; 101.259; 90
2265.03Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547511 CIFC23 H41 F3 N3 O3 SP b c a17.684; 17.465; 33.978
90; 90; 90
10494Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547512 CIFC20 H33 F6 N3 O6 S2P 1 21/c 115.6706; 12.5278; 14.3707
90; 110.805; 90
2637.3Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547513 CIFC26 H44 F6 N4 O6 S2P n a 2123.095; 13.2861; 10.6916
90; 90; 90
3280.6Mandal, Debdeep; Dolai, Ramapada; Chrysochos, Nicolas; Kalita, Pankaj; Kumar, Ravi; Dhara, Debabrata; Maiti, Avijit; Narayanan, Ramakirushnan Suriya; Rajaraman, Gopalan; Schulzke, Carola; Chandrasekhar, Vadapalli; Jana, Anukul
Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications.
Organic letters, 2017, 19, 5605-5608
1547514 CIFC13 H15 N O2P -17.3581; 9.0853; 9.4911
108.041; 101.319; 98.946
575.42Shemet, Andrej; Carreira, Erick M.
Total Synthesis of (-)-Rhazinilam and Formal Synthesis of (+)-Eburenine and (+)-Aspidospermidine: Asymmetric Cu-Catalyzed Propargylic Substitution.
Organic letters, 2017, 19, 5529-5532
1547515 CIFC21 H26 N2 O2P 1 21/n 18.3072; 23.509; 8.9287
90; 98.124; 90
1726.2Shemet, Andrej; Carreira, Erick M.
Total Synthesis of (-)-Rhazinilam and Formal Synthesis of (+)-Eburenine and (+)-Aspidospermidine: Asymmetric Cu-Catalyzed Propargylic Substitution.
Organic letters, 2017, 19, 5529-5532
1547527 CIFC31 H30 Br F N2 O8 SP 1 21 113.794; 7.4068; 15.014
90; 99.751; 90
1511.8Li, Hanyuan; Luo, Jiesi; Li, Bojuan; Yi, Xizhen; He, Zhengjie
Enantioselective [4 + 1]-Annulation of α,β-Unsaturated Imines with Allylic Carbonates Catalyzed by a Hybrid P-Chiral Phosphine Oxide-Phosphine.
Organic letters, 2017, 19, 5637-5640
1547528 CIFC27 H22 Br Cl N2 O6 SP -17.762; 12.126; 14.58
100.941; 98.338; 93.2
1328.2Li, Hanyuan; Luo, Jiesi; Li, Bojuan; Yi, Xizhen; He, Zhengjie
Enantioselective [4 + 1]-Annulation of α,β-Unsaturated Imines with Allylic Carbonates Catalyzed by a Hybrid P-Chiral Phosphine Oxide-Phosphine.
Organic letters, 2017, 19, 5637-5640
1547529 CIFC39 H35 N O2 P2P 1 21 18.275; 22.39; 9.224
90; 109.92; 90
1607Li, Hanyuan; Luo, Jiesi; Li, Bojuan; Yi, Xizhen; He, Zhengjie
Enantioselective [4 + 1]-Annulation of α,β-Unsaturated Imines with Allylic Carbonates Catalyzed by a Hybrid P-Chiral Phosphine Oxide-Phosphine.
Organic letters, 2017, 19, 5637-5640
1547530 CIFC10 H7 Br N2 OP 1 21/n 17.1898; 19.2245; 7.5937
90; 113.318; 90
963.87Wang, Qing-Qing; Xu, Kun; Jiang, Yang-Ye; Liu, Yong-Guo; Sun, Bao-Guo; Zeng, Cheng-Chu
Electrocatalytic Minisci Acylation Reaction of N-Heteroarenes Mediated by NH4I.
Organic letters, 2017, 19, 5517-5520
1547551 CIFC16 H12 O SP 21 21 217.5278; 12.6117; 13.7183
90; 90; 90
1302.39Nguyen, Thanh Binh; Retailleau, Pascal
DIPEA-Promoted Reaction of 2-Nitrochalcones with Elemental Sulfur: An Unusual Approach to 2-Benzoylbenzothiophenes.
Organic letters, 2017, 19, 4858-4860
1547552 CIFC14 H16 N2 OP c c n14.952; 18.354; 9.4968
90; 90; 90
2606.2Zhu, Nengbo; Wang, Ting; Ge, Liang; Li, Yajun; Zhang, Xinhao; Bao, Hongli
γ-Amino Butyric Acid (GABA) Synthesis Enabled by Copper-Catalyzed Carboamination of Alkenes.
Organic letters, 2017, 19, 4718-4721
1547553 CIFC18 H18.74 N2 O1.37P 1 21/c 116.4116; 5.5613; 17.4699
90; 105.341; 90
1537.66Zhu, Nengbo; Wang, Ting; Ge, Liang; Li, Yajun; Zhang, Xinhao; Bao, Hongli
γ-Amino Butyric Acid (GABA) Synthesis Enabled by Copper-Catalyzed Carboamination of Alkenes.
Organic letters, 2017, 19, 4718-4721
1547554 CIFC26 H29 O PP 1 21/c 17.3313; 19.6104; 15.1854
90; 98.05; 90
2161.69Hu, Zhengsong; Tian, Rongqiang; Zhao, Kang; Liu, Yanjie; Duan, Zheng; Mathey, François
Generation and Trapping of a 1-Phosphafulvene: An Illustration of the P═C/C═C Analogy.
Organic letters, 2017, 19, 5004-5006
1547555 CIFC23 H23 Br O3P 1 21 15.5574; 11.2786; 16.5421
90; 99.257; 90
1023.35Cheng, Yuyu; Han, Yuzhe; Li, Pengfei
Organocatalytic Enantioselective [1 + 4] Annulation of Morita-Baylis-Hillman Carbonates with Electron-Deficient Olefins: Access to Chiral 2,3-Dihydrofuran Derivatives.
Organic letters, 2017, 19, 4774-4777
1547556 CIFC26 H23 N OP 1 21/c 19.934; 22.154; 8.9741
90; 94.349; 90
1969.3Gao, Shang; Liu, Hao; Yang, Chi; Fu, Zhiyuan; Yao, Hequan; Lin, Aijun
Accessing 1,3-Dienes via Palladium-Catalyzed Allylic Alkylation of Pronucleophiles with Skipped Enynes.
Organic letters, 2017, 19, 4710-4713
1547557 CIFC37 H32 N2 O3P -17.3961; 14.159; 14.7965
113.245; 93.815; 94.009
1412.7Gao, Shang; Liu, Hao; Yang, Chi; Fu, Zhiyuan; Yao, Hequan; Lin, Aijun
Accessing 1,3-Dienes via Palladium-Catalyzed Allylic Alkylation of Pronucleophiles with Skipped Enynes.
Organic letters, 2017, 19, 4710-4713
1547558 CIFC17 H17 N O3 SP 1 21/c 19.8615; 12.1461; 14.1071
90; 107.15; 90
1614.6Lee, Dabon; Kim, Sang Min; Hirao, Hajime; Hong, Soon Hyeok
Gold(I)/Gold(III)-Catalyzed Selective Synthesis of N-Sulfonyl Enaminone Isomers from Sulfonamides and Ynones via Two Distinct Reaction Pathways.
Organic letters, 2017, 19, 4734-4737
1547559 CIFC15 H14 O5P 1 21 19.82867; 6.11703; 11.6406
90; 100.472; 90
688.2Lehner, Verena; Davies, Huw M. L.; Reiser, Oliver
Rh(II)-Catalyzed Cyclopropanation of Furans and Its Application to the Total Synthesis of Natural Product Derivatives.
Organic letters, 2017, 19, 4722-4725
1547560 CIFC14 H16 O4P 1 21/c 18.22602; 15.4712; 10.0483
90; 103.364; 90
1244.18Lehner, Verena; Davies, Huw M. L.; Reiser, Oliver
Rh(II)-Catalyzed Cyclopropanation of Furans and Its Application to the Total Synthesis of Natural Product Derivatives.
Organic letters, 2017, 19, 4722-4725
1547561 CIFC13 H12 O3P 21 21 218.1779; 8.8079; 15.2085
90; 90; 90
1095.47Lehner, Verena; Davies, Huw M. L.; Reiser, Oliver
Rh(II)-Catalyzed Cyclopropanation of Furans and Its Application to the Total Synthesis of Natural Product Derivatives.
Organic letters, 2017, 19, 4722-4725
1547562 CIFC15 H14 O5C 1 2 116.4819; 5.7733; 14.4387
90; 106.49; 90
1317.4Lehner, Verena; Davies, Huw M. L.; Reiser, Oliver
Rh(II)-Catalyzed Cyclopropanation of Furans and Its Application to the Total Synthesis of Natural Product Derivatives.
Organic letters, 2017, 19, 4722-4725
1547563 CIFC40 H35 Br N4 O3P -110.6766; 10.7779; 15.8861
79.719; 73.665; 77.959
1701.6Liu, Honglei; Jia, Hao; Wang, Bo; Xiao, Yumei; Guo, Hongchao
Synthesis of Spirobidihydropyrazole through Double 1,3-Dipolar Cycloaddition of Nitrilimines with Allenoates.
Organic letters, 2017, 19, 4714-4717
1547564 CIFC39 H34 N4 O2P 1 21/c 19.704; 18.77; 17
90; 102.647; 90
3021.3Liu, Honglei; Jia, Hao; Wang, Bo; Xiao, Yumei; Guo, Hongchao
Synthesis of Spirobidihydropyrazole through Double 1,3-Dipolar Cycloaddition of Nitrilimines with Allenoates.
Organic letters, 2017, 19, 4714-4717
1547565 CIFC46 H11 Cl5 F20 S4P 18.198; 10.441; 13.934
101.832; 96.687; 104.041
1115Panchal, Santosh P.; Anand, Venkataramanarao G.
Oxidative Transformation of a Tetrathia S-Confused Isophlorin into Porphyrin Cation.
Organic letters, 2017, 19, 4854-4857
1547566 CIFC4 H4 N2 O2P 1 n 13.8868; 5.4329; 10.8693
90; 97.068; 90
227.78Rozen, Shlomo; Shaffer, Avshalom
Synthesis of N,N-Dioxopyridazines.
Organic letters, 2017, 19, 4707-4709
1547567 CIFC15 H14 O3 SP 17.8451; 8.3042; 11.06
76.583; 88.533; 75.925
679.46Xia, Jingzhao; Nie, Yu; Yang, Guoqiang; Liu, Yangang; Zhang, Wanbin
Iridium-Catalyzed Asymmetric Hydrogenation of 2H-Chromenes: A Highly Enantioselective Approach to Isoflavan Derivatives.
Organic letters, 2017, 19, 4884-4887
1547568 CIFC15 H13 Cl OP 1 21 15.7624; 22.9736; 9.5587
90; 106.003; 90
1216.37Xia, Jingzhao; Nie, Yu; Yang, Guoqiang; Liu, Yangang; Zhang, Wanbin
Iridium-Catalyzed Asymmetric Hydrogenation of 2H-Chromenes: A Highly Enantioselective Approach to Isoflavan Derivatives.
Organic letters, 2017, 19, 4884-4887
1547569 CIFC33 H28 P2 S2P -110.179; 10.178; 14.35
95.75; 95.75; 107.27
1399Otomura, Nobutaka; Okugawa, Yuto; Hirano, Koji; Miura, Masahiro
vic-Diphosphination of Alkenes with Silylphosphine under Visible-Light-Promoted Photoredox Catalysis.
Organic letters, 2017, 19, 4802-4805
1547570 CIFC20 H30 O3P 1 21 110.1944; 6.53348; 13.5748
90; 95.12; 90
900.54Xu, Bo; Xun, Wen; Wang, Tingzhong; Qiu, Fayang G.
Total Synthesis of (+)-Aplykurodinone-1.
Organic letters, 2017, 19, 4861-4863
1547571 CIFC32 H50 Cu N4 O10P -110.8093; 12.3197; 14.2754
88.759; 86.694; 66.762
1743.9Tan, Guangying; Zhang, Luoqiang; Liao, Xingrong; Shi, Yang; Wu, Yimin; Yang, Yudong; You, Jingsong
Copper- or Nickel-Enabled Oxidative Cross-Coupling of Unreactive C(sp(3))-H Bonds with Azole C(sp(2))-H Bonds: Rapid Access to β-Azolyl Propanoic Acid Derivatives.
Organic letters, 2017, 19, 4830-4833
1547572 CIFC17 H23 Br OP 21 21 217.4193; 12.1143; 17.167
90; 90; 90
1543Grayfer, Tatyana D.; Retailleau, Pascal; Dodd, Robert H.; Dubois, Joëlle; Cariou, Kevin
Chemodivergent, Tunable, and Selective Iodine(III)-Mediated Bromo-Functionalizations of Polyprenoids.
Organic letters, 2017, 19, 4766-4769
1547573 CIFC17 H23 BrP -17.4409; 10.1018; 11.3589
68.534; 75.635; 69.502
737.19Grayfer, Tatyana D.; Retailleau, Pascal; Dodd, Robert H.; Dubois, Joëlle; Cariou, Kevin
Chemodivergent, Tunable, and Selective Iodine(III)-Mediated Bromo-Functionalizations of Polyprenoids.
Organic letters, 2017, 19, 4766-4769
1547574 CIFC16 H21 BrI 1 2/a 119.772; 6.1368; 23.6786
90; 94.152; 90
2865.5Grayfer, Tatyana D.; Retailleau, Pascal; Dodd, Robert H.; Dubois, Joëlle; Cariou, Kevin
Chemodivergent, Tunable, and Selective Iodine(III)-Mediated Bromo-Functionalizations of Polyprenoids.
Organic letters, 2017, 19, 4766-4769
1547575 CIFC25 H22 N2 O6P 1 21 111.5902; 7.8925; 25.534
90; 96.954; 90
2318.6Yuan, Yang; Yu, Bo; Bai, Xing-Feng; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Cao, Jian; Xu, Li-Wen
Asymmetric Synthesis of Glutamic Acid Derivatives by Silver-Catalyzed Conjugate Addition-Elimination Reactions.
Organic letters, 2017, 19, 4896-4899
1547576 CIFC21 H19 Br N2 O6P 17.04; 7.063; 10.762
83.24; 79.64; 79.5
515.6Yuan, Yang; Yu, Bo; Bai, Xing-Feng; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Cao, Jian; Xu, Li-Wen
Asymmetric Synthesis of Glutamic Acid Derivatives by Silver-Catalyzed Conjugate Addition-Elimination Reactions.
Organic letters, 2017, 19, 4896-4899
1547577 CIFC37 H26 O2 SP b c n13.7489; 12.7062; 34.5595
90; 90; 90
6037.4Wang, Ming; Chen, Shihao; Jiang, Xuefeng
Construction of Functionalized Annulated Sulfone via SO2/I Exchange of Cyclic Diaryliodonium Salts.
Organic letters, 2017, 19, 4916-4919
1547578 CIFC15 H12 O2 SP 1 21/c 111.6687; 8.3221; 12.6959
90; 101.677; 90
1207.36Wang, Ming; Chen, Shihao; Jiang, Xuefeng
Construction of Functionalized Annulated Sulfone via SO2/I Exchange of Cyclic Diaryliodonium Salts.
Organic letters, 2017, 19, 4916-4919
1547579 CIFC27 H18 O7P 1 21/n 15.539; 15.1853; 24.1953
90; 91.286; 90
2034.59Sasaki, Sayaka; Azuma, Eriko; Sasamori, Takahiro; Tokitoh, Norihiro; Kuramochi, Kouji; Tsubaki, Kazunori
Formation of Phenalenone Skeleton by an Unusual Rearrangement Reaction.
Organic letters, 2017, 19, 4846-4849
1547580 CIFC15 H20 F N O3P 21 21 215.0624; 10.961; 26.361
90; 90; 90
1462.7Zhang, Wandi; Chen, Weijie; Xiao, Hongde; Krische, Michael J.
Carbonyl anti-(α-Amino)allylation via Ruthenium Catalyzed Hydrogen Autotransfer: Use of an Acetylenic Pyrrole as an Allylmetal Pronucleophile.
Organic letters, 2017, 19, 4876-4879
1547581 CIFC51 H42 Cl2 N4 PdP 21 21 2113.308; 15.883; 19.472
90; 90; 90
4116Nozawa, Ryo; Shinokubo, Hiroshi
Synthesis and Properties of meso-Arylated Corrphycenes.
Organic letters, 2017, 19, 4928-4931
1547582 CIFC19 H19 Br N2 OP n a 2115.3885; 7.1222; 30.3
90; 90; 90
3320.9Zhao, Jie; Zhao, Xiao-Jing; Cao, Pei; Liu, Ji-Kai; Wu, Bin
Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds.
Organic letters, 2017, 19, 4880-4883
1547583 CIFC16 H20 N2 OP 21 21 216.1299; 13.8742; 15.703
90; 90; 90
1335.5Zhao, Jie; Zhao, Xiao-Jing; Cao, Pei; Liu, Ji-Kai; Wu, Bin
Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds.
Organic letters, 2017, 19, 4880-4883
1547584 CIFC19 H20 N2 OP c a 2113.7527; 9.8191; 22.826
90; 90; 90
3082.4Zhao, Jie; Zhao, Xiao-Jing; Cao, Pei; Liu, Ji-Kai; Wu, Bin
Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds.
Organic letters, 2017, 19, 4880-4883
1547585 CIFC13 H14 N2 O3P -16.1525; 9.8018; 10.5143
99.556; 103.113; 102.27
587.94Zhao, Jie; Zhao, Xiao-Jing; Cao, Pei; Liu, Ji-Kai; Wu, Bin
Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds.
Organic letters, 2017, 19, 4880-4883
1547586 CIFC15 H18 N2 O3P 1 21/c 113.8893; 8.4698; 12.0582
90; 107.287; 90
1354.4Zhao, Jie; Zhao, Xiao-Jing; Cao, Pei; Liu, Ji-Kai; Wu, Bin
Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds.
Organic letters, 2017, 19, 4880-4883
1547587 CIFC21 H26 N2 O3 SP 1 21 16.3959; 8.7834; 17.916
90; 100.037; 90
991.08Mwenda, Edward T.; Nguyen, Hien M.
Enantioselective Synthesis of 1,2-Diamines Containing Tertiary and Quaternary Centers through Rhodium-Catalyzed DYKAT of Racemic Allylic Trichloroacetimidates.
Organic letters, 2017, 19, 4814-4817
1547588 CIFC21 H26 N2 O3 SP 1 21 16.3983; 8.7684; 17.9628
90; 99.675; 90
993.43Mwenda, Edward T.; Nguyen, Hien M.
Enantioselective Synthesis of 1,2-Diamines Containing Tertiary and Quaternary Centers through Rhodium-Catalyzed DYKAT of Racemic Allylic Trichloroacetimidates.
Organic letters, 2017, 19, 4814-4817
1547589 CIFC26 H21 Cl N3 O3P 21 21 215.9123; 16.6068; 23.602
90; 90; 90
2317.35Wang, Jie; Wang, Pengxin; Wang, Linqing; Li, Dan; Wang, Kezhou; Wang, Yuan; Zhu, Haiyong; Yang, Dongxu; Wang, Rui
Nickel-Mediated Asymmetric Allylic Alkylation between Nitroallylic Acetates and Acyl Imidazoles.
Organic letters, 2017, 19, 4826-4829
1547590 CIFC8 H8 F4 N2 O4P -18.8731; 9.0666; 15.314
91.196; 99.999; 115.544
1088.3Schmitt, Etienne; Bouvet, Sébastien; Pégot, Bruce; Panossian, Armen; Vors, Jean-Pierre; Pazenok, Sergii; Magnier, Emmanuel; Leroux, Frédéric R
Fluoroalkyl Amino Reagents for the Introduction of the Fluoro(trifluoromethoxy)methyl Group onto Arenes and Heterocycles.
Organic letters, 2017, 19, 4960-4963
1547599 CIFC19 H17 Fe N O2P 1 21/c 19.4767; 15.378; 10.8957
90; 111.006; 90
1482.3Liu, Yang; Xu, Jiancong; Zhang, Jinling; Xu, Xiaohua; Jin, Zhong
Intramolecular Direct C-H Arylation via a Metallocenic Radical Pathway: Stereospecific Approach to Planar-Chiral Ferrocenes.
Organic letters, 2017, 19, 5709-5712
1547600 CIFC18 H13 Fe N O3P 1 21/c 16.067; 13.753; 17.502
90; 99.914; 90
1438.6Liu, Yang; Xu, Jiancong; Zhang, Jinling; Xu, Xiaohua; Jin, Zhong
Intramolecular Direct C-H Arylation via a Metallocenic Radical Pathway: Stereospecific Approach to Planar-Chiral Ferrocenes.
Organic letters, 2017, 19, 5709-5712
1547601 CIFC19 H17 Fe N OP 1 21/c 119.945; 8.3402; 17.264
90; 91.165; 90
2871.2Liu, Yang; Xu, Jiancong; Zhang, Jinling; Xu, Xiaohua; Jin, Zhong
Intramolecular Direct C-H Arylation via a Metallocenic Radical Pathway: Stereospecific Approach to Planar-Chiral Ferrocenes.
Organic letters, 2017, 19, 5709-5712
1547602 CIFC11 H9 F2 N O2P -15.5743; 8.0878; 12.3099
107.2; 93.657; 103.638
509.85Peng, Shan-Qing; Zhang, Xiao-Wei; Zhang, Long; Hu, Xiang-Guo
Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect.
Organic letters, 2017, 19, 5689-5692
1547603 CIFC24 H20 F3 N O2P -19.715; 9.964; 21.348
90.371; 94.727; 104.841
1989.9Peng, Shan-Qing; Zhang, Xiao-Wei; Zhang, Long; Hu, Xiang-Guo
Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect.
Organic letters, 2017, 19, 5689-5692
1547604 CIFC9 H7 F2 N O4P 6515.9119; 15.9119; 20.3939
90; 90; 120
4471.7Peng, Shan-Qing; Zhang, Xiao-Wei; Zhang, Long; Hu, Xiang-Guo
Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect.
Organic letters, 2017, 19, 5689-5692
1547605 CIFC13 H12 F3 N O4P 1 21/n 112.455; 6.376; 16.642
90; 96.688; 90
1312.6Peng, Shan-Qing; Zhang, Xiao-Wei; Zhang, Long; Hu, Xiang-Guo
Esterification of Carboxylic Acids with Difluoromethyl Diazomethane and Interrupted Esterification with Trifluoromethyl Diazomethane: A Fluorine Effect.
Organic letters, 2017, 19, 5689-5692
1547606 CIFC18 H12P 1 21/c 111.7846; 6.1519; 8.0708
90; 92.61; 90
584.51Murai, Masahito; Iba, Shinji; Ota, Hiromi; Takai, Kazuhiko
Azulene-Fused Linear Polycyclic Aromatic Hydrocarbons with Small Bandgap, High Stability, and Reversible Stimuli Responsiveness.
Organic letters, 2017, 19, 5585-5588
1547611 CIFC19 H19 Br O3P 1 21 17.7292; 25.126; 9.073
90; 110.817; 90
1647He, Rui; Liu, Penglin; Huo, Xiaohong; Zhang, Wanbin
Ir/Zn Dual Catalysis: Enantioselective and Diastereodivergent α-Allylation of Unprotected α-Hydroxy Indanones.
Organic letters, 2017, 19, 5513-5516
1547612 CIFC19 H18 O2P 21 21 215.8811; 13.6299; 18.7137
90; 90; 90
1500.07He, Rui; Liu, Penglin; Huo, Xiaohong; Zhang, Wanbin
Ir/Zn Dual Catalysis: Enantioselective and Diastereodivergent α-Allylation of Unprotected α-Hydroxy Indanones.
Organic letters, 2017, 19, 5513-5516
1547613 CIFC18 H15 Br O2P 21 21 218.6567; 13.8347; 25.4021
90; 90; 90
3042.23He, Rui; Liu, Penglin; Huo, Xiaohong; Zhang, Wanbin
Ir/Zn Dual Catalysis: Enantioselective and Diastereodivergent α-Allylation of Unprotected α-Hydroxy Indanones.
Organic letters, 2017, 19, 5513-5516
1547614 CIFC25 H21 N O5R 3 :H31.8047; 31.8047; 11.8143
90; 90; 120
10349.5He, Rui; Liu, Penglin; Huo, Xiaohong; Zhang, Wanbin
Ir/Zn Dual Catalysis: Enantioselective and Diastereodivergent α-Allylation of Unprotected α-Hydroxy Indanones.
Organic letters, 2017, 19, 5513-5516
1547615 CIFC33 H20 Cl7 N OP 1 21/c 112.1851; 15.4614; 17.05
90; 102.559; 90
3135.3Shankar, Majji; Guntreddi, Tirumaleswararao; Ramesh, E.; Sahoo, Akhila K.
Transformable Sulfoximine Assisted One-Pot Double Annulation of Vinylic C-H Bonds with Unactivated Alkynes.
Organic letters, 2017, 19, 5665-5668
1547616 CIFC22 H19 N OP 1 21/c 110.19; 17.463; 9.5878
90; 106.025; 90
1639.8Shankar, Majji; Guntreddi, Tirumaleswararao; Ramesh, E.; Sahoo, Akhila K.
Transformable Sulfoximine Assisted One-Pot Double Annulation of Vinylic C-H Bonds with Unactivated Alkynes.
Organic letters, 2017, 19, 5665-5668
1547639 CIFC17 H18 N2 O4 SP 21 21 217.426; 11.292; 20.718
90; 90; 90
1737.3Qian, Xue-Wei; Xue, Ze-Jian; Zhao, Qian; Cui, Zhe; Chen, Ya-Jing; Feng, Chen-Guo; Lin, Guo-Qiang
Enantioselective Rhodium-Catalyzed Alkenylation of Aliphatic Imines.
Organic letters, 2017, 19, 5601-5604
1547640 CIFC22 H21 N O4P -16.8929; 7.6318; 19.0999
100.04; 92.095; 110.687
920.31Kim, Hyunseok; Kim, Sanghyuck; Kim, Jiyeon; Son, Jeong-Yu; Baek, Yonghyeon; Um, Kyusik; Lee, Phil Ho
One-Pot Synthesis of Indolizines via Sequential Rhodium-Catalyzed [2 + 1]-Cyclopropanation, Palladium-Catalyzed Ring Expansion, and Oxidation Reactions from Pyridotriazoles and 1,3-Dienes.
Organic letters, 2017, 19, 5677-5680
1547641 CIFC27 H23 N O2P -19.125; 11.0174; 11.6902
102.952; 102.365; 105.581
1055.1Kim, Hyunseok; Kim, Sanghyuck; Kim, Jiyeon; Son, Jeong-Yu; Baek, Yonghyeon; Um, Kyusik; Lee, Phil Ho
One-Pot Synthesis of Indolizines via Sequential Rhodium-Catalyzed [2 + 1]-Cyclopropanation, Palladium-Catalyzed Ring Expansion, and Oxidation Reactions from Pyridotriazoles and 1,3-Dienes.
Organic letters, 2017, 19, 5677-5680
1547663 CIFC23 H31 Br N3 PP -19.1345; 14.6643; 18.0325
92.023; 96.2988; 105.032
2313.62Tien, Chieh-Hung; Adams, Matt R.; Ferguson, Michael J.; Johnson, Erin R.; Speed, Alexander W. H.
Hydroboration Catalyzed by 1,2,4,3-Triazaphospholenes.
Organic letters, 2017, 19, 5565-5568
1547664 CIFC29 H48 O3P 21 21 213.7185; 20.7124; 20.7597
90; 90; 90
5898.72Wang, Chao; Huo, Xiao-Kui; Luan, Zhi-Lin; Cao, Fei; Tian, Xiang-Ge; Zhao, Xin-Yu; Sun, Cheng-Peng; Feng, Lei; Ning, Jing; Zhang, Bao-Jing; Ma, Xiao-Chi
Alismanin A, a Triterpenoid with a C34 Skeleton from Alisma orientale as a Natural Agonist of Human Pregnane X Receptor.
Organic letters, 2017, 19, 5645-5648
1547665 CIFC150 H138 N14 O6P -117.226; 22.283; 24.02
117.27; 92.88; 96.46
8089Hwang, Ji Young; Jeon, Hae-Geun; Choi, Ye Rin; Kim, Junyoung; Kang, Philjae; Lee, Seungwon; Jeong, Kyu-Sung
Aromatic Hybrid Foldamer with a Hydrophilic Helical Cavity Capable of Encapsulating Glucose.
Organic letters, 2017, 19, 5625-5628
1547666 CIFC18 H22 N16 O2P 1 21/c 116.625; 13.626; 10.32
90; 92.77; 90
2335.1Kim, Illan; Ko, Kyoung Chul; Lee, Woo Ram; Cho, Jihee; Moon, Jong Hun; Moon, Dohyun; Sharma, Amit; Lee, Jin Yong; Kim, Jong Seung; Kim, Sanghee
Calix[n]triazoles and Related Conformational Studies.
Organic letters, 2017, 19, 5509-5512
1547667 CIFC12 H12 N12P 1 21/c 18.7126; 5.5052; 14.9132
90; 101.476; 90
701.01Kim, Illan; Ko, Kyoung Chul; Lee, Woo Ram; Cho, Jihee; Moon, Jong Hun; Moon, Dohyun; Sharma, Amit; Lee, Jin Yong; Kim, Jong Seung; Kim, Sanghee
Calix[n]triazoles and Related Conformational Studies.
Organic letters, 2017, 19, 5509-5512
1547668 CIFC18 H22 O2P 21 21 216.2248; 21.607; 8.7927
90; 90; 90
3082.5Kang, Houng; Lee, Young Eun; Reddy, Peddiahgari Vasu Govardhana; Dey, Sangeeta; Allen, Scott E.; Niederer, Kyle A.; Sung, Paul; Hewitt, Kirsten; Torruellas, Carilyn; Herling, Madison R.; Kozlowski, Marisa C.
Asymmetric Oxidative Coupling of Phenols and Hydroxycarbazoles.
Organic letters, 2017, 19, 5505-5508
1547673 CIFC18 H14 N3 O0.5 SP -18.2595; 10.2305; 10.237
98.393; 113.578; 95.939
771.71Ramanathan, Mani; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung
Synthesis of Substituted Quinazolin-4(3H)-imines From Aryldiazonium Salts, Nitriles and 2-Cyanoanilines via A Metal-Free Tandem Approach.
Organic letters, 2017, 19, 5840-5843
1547674 CIFC26 H16 Cl O2 PP -18.2205; 11.1612; 11.4544
106.106; 97.928; 93.594
994.4Zhao, Xu; Gan, Zhenjie; Hu, Chaopeng; Duan, Zheng; Mathey, François
Planar Polycyclic Oxaphosphoranes Incorporating a Benzophosphole Unit.
Organic letters, 2017, 19, 5814-5817
1547675 CIFC33 H25 O PP -112.3745; 13.9516; 15.5108
90.361; 108.098; 97.969
2517.32Zhao, Xu; Gan, Zhenjie; Hu, Chaopeng; Duan, Zheng; Mathey, François
Planar Polycyclic Oxaphosphoranes Incorporating a Benzophosphole Unit.
Organic letters, 2017, 19, 5814-5817
1547676 CIFC26 H21 Cl2 O PP -19.6822; 10.6345; 11.7489
97.498; 106.46; 93.254
1144.63Zhao, Xu; Gan, Zhenjie; Hu, Chaopeng; Duan, Zheng; Mathey, François
Planar Polycyclic Oxaphosphoranes Incorporating a Benzophosphole Unit.
Organic letters, 2017, 19, 5814-5817
1547677 CIFC26 H18 Cl O PP 1 21/n 19.4124; 14.7338; 14.2292
90; 90.71; 90
1973.16Zhao, Xu; Gan, Zhenjie; Hu, Chaopeng; Duan, Zheng; Mathey, François
Planar Polycyclic Oxaphosphoranes Incorporating a Benzophosphole Unit.
Organic letters, 2017, 19, 5814-5817
1547678 CIFC16 H15 N O3P b c a11.8722; 8.4475; 26.7964
90; 90; 90
2687.42Chen, Rongxiang; Zhao, Yanwei; Fang, Shangwen; Long, Wenhao; Sun, Hongmei; Wan, Xiaobing
Coupling Reaction of Cu-Based Carbene and Nitroso Radical: A Tandem Reaction To Construct Isoxazolines.
Organic letters, 2017, 19, 5896-5899
1547695 CIFC12 H13 I N2 O3P -18.5985; 8.9813; 10.1508
113.998; 91.78; 111.582
650.7Ziegler, Dorothée S; Greiner, Robert; Lumpe, Henning; Kqiku, Laura; Karaghiosoff, Konstantin; Knochel, Paul
Directed Zincation or Magnesiation of the 2-Pyridone and 2,7-Naphthyridone Scaffold Using TMP Bases.
Organic letters, 2017, 19, 5760-5763
1547696 CIFC18 H13 I N2 O4P 21 21 217.854; 11.693; 18.074
90; 90; 90
1659.9Toda, Yasunori; Gomyou, Shuto; Tanaka, Shoya; Komiyama, Yutaka; Kikuchi, Ayaka; Suga, Hiroyuki
Tetraarylphosphonium Salt-Catalyzed Synthesis of Oxazolidinones from Isocyanates and Epoxides.
Organic letters, 2017, 19, 5786-5789
1547697 CIFC26 H37 Br O5 SiP -17.79; 9.6934; 18.868
84.627; 84.464; 67.565
1308.27Abe, Hideki; Ogura, Yuta; Kobayashi, Toyoharu; Ito, Hisanaka
Total Synthesis of Paralemnolide A.
Organic letters, 2017, 19, 5996-5999
1547698 CIFC21 H25 Br O4P 1 21/n 19.9141; 18.7872; 10.6013
90; 91.608; 90
1973.8Abe, Hideki; Ogura, Yuta; Kobayashi, Toyoharu; Ito, Hisanaka
Total Synthesis of Paralemnolide A.
Organic letters, 2017, 19, 5996-5999
1547699 CIFC20 H35 Br O3 SiP -17.5249; 10.273; 15.343
104.399; 103.098; 95.903
1102.87Abe, Hideki; Ogura, Yuta; Kobayashi, Toyoharu; Ito, Hisanaka
Total Synthesis of Paralemnolide A.
Organic letters, 2017, 19, 5996-5999
1547700 CIFC17 H20 F2 O2P c a 219.8218; 12.5329; 12.4155
90; 90; 90
1528.3Sha, Wanxing; Ni, Shengyang; Han, Jianlin; Pan, Yi
Access to Alkyl-Substituted Lactone via Photoredox-Catalyzed Alkylation/Lactonization of Unsaturated Carboxylic Acids.
Organic letters, 2017, 19, 5900-5903
1547701 CIFC21 H28 Br N O7P 15.8465; 9.7587; 9.8846
89.343; 87.738; 86.3034
562.324Horwitz, Matthew A.; Fulton, Jennifer L.; Johnson, Jeffrey S.
Enantio- and Diastereoselective Organocatalytic Conjugate Additions of Nitroalkanes to Enone Diesters.
Organic letters, 2017, 19, 5783-5785
1547702 CIFC17 H22 O5P 21 21 219.7097; 12.1431; 12.8881
90; 90; 90
1519.58Chen, Keliang; Zhang, Xuwen; Sun, Weiguang; Liu, Junjun; Yang, Jing; Chen, Chunmei; Liu, Xiulan; Gao, Limin; Wang, Jianping; Li, Hua; Luo, Zengwei; Xue, Yongbo; Zhu, Hucheng; Zhang, Yonghui
Manginoids A-G: Seven Monoterpene-Shikimate-Conjugated Meroterpenoids with a Spiro Ring System from Guignardia mangiferae.
Organic letters, 2017, 19, 5956-5959
1547703 CIFC24 H25 Cl3 Ir N4P n a 2121.597; 7.285; 16.615
90; 90; 90
2614.1Liang, Ran; Li, Shun; Wang, Rongzhou; Lu, Lei; Li, Feng
N-Methylation of Amines with Methanol Catalyzed by a Cp*Ir Complex Bearing a Functional 2,2'-Bibenzimidazole Ligand.
Organic letters, 2017, 19, 5790-5793
1547704 CIFC27 H20 O7 SP 21 21 2110.2354; 14.6975; 16.2321
90; 90; 90
2441.9Doyle, Lisa M.; O'Sullivan, Shane; Di Salvo, Claudia; McKinney, Michelle; McArdle, Patrick; Murphy, Paul V.
Stereoselective Epimerizations of Glycosyl Thiols.
Organic letters, 2017, 19, 5802-5805
1547726 CIFC18 H24 N O4P -110.0478; 10.1851; 10.8815
95.641; 114.147; 108.576
929Edwards, Peter M.; Schafer, Laurel L.
In Situ Generation of a Regio- and Diastereoselective Hydroaminoalkylation Catalyst Using Commercially Available Starting Materials.
Organic letters, 2017, 19, 5720-5723
1547727 CIFC15 H24 Cl N OP n a 2121.142; 9.442; 14.826
90; 90; 90
2959.6Edwards, Peter M.; Schafer, Laurel L.
In Situ Generation of a Regio- and Diastereoselective Hydroaminoalkylation Catalyst Using Commercially Available Starting Materials.
Organic letters, 2017, 19, 5720-5723
1547728 CIFC28 H21 N3 O3P -18.3542; 11.7504; 11.9494
102.671; 106.404; 97.121
1076Manoharan, Ramasamy; Jeganmohan, Masilamani
Cobalt-Catalyzed Oxidative Cyclization of Benzamides with Maleimides: Synthesis of Isoindolone Spirosuccinimides.
Organic letters, 2017, 19, 5884-5887
1547729 CIFC18 H18 N3 O4 PP 1 21 19.49772; 7.06251; 13.2196
90; 104.074; 90
860.13Huang, Nan; Zou, Liangliang; Peng, Yungui
Enantioselective 1,3-Dipolar Cycloaddition of Methyleneindolinones with α-Diazomethylphosphonate to Access Chiral Spiro-phosphonylpyrazoline-oxindoles Catalyzed by Tertiary Amine Thiourea and 1,5-Diazabicyclo[4.3.0]non-5-ene.
Organic letters, 2017, 19, 5806-5809
1547732 CIFC23 H21 N O3 SP -19.0699; 13.9562; 17.516
88.185; 78.4; 72.259
2067.6Nagamoto, Midori; Fukuda, Jun-Ichi; Hatano, Miyuki; Yorimitsu, Hideki; Nishimura, Takahiro
Hydroxoiridium-Catalyzed Hydroarylation of Alkynes and Bicycloalkenes with N-Sulfonylbenzamides.
Organic letters, 2017, 19, 5952-5955
1547733 CIFC18 H14 O2P -17.7485; 8.638; 11.316
78.953; 72.382; 65.252
653.7Fan, Jinming; Wang, Tao; Li, Chenchen; Wang, Rui; Lei, Xiaoyu; Liang, Yong; Zhang, Zunting
Synthesis of Benzoaryl-5-yl(2-hydroxyphenyl)methanones via Photoinduced Rearrangement of (E)-3-Arylvinyl-4H-chromen-4-ones.
Organic letters, 2017, 19, 5984-5987
1547734 CIFC24 H30 N4 O2I -417.5556; 17.5556; 14.122
90; 90; 90
4352.4Zhang, Shang-Shi; Xia, Jie; Wu, Jia-Qiang; Liu, Xu-Ge; Zhou, Chu-Jun; Lin, E.; Li, Qingjiang; Huang, Shi-Liang; Wang, Honggen
Three-Component Catalytic Carboxygenation of Activated Alkenes Enabled by Bimetallic Rh(III)/Cu(II) Catalysis.
Organic letters, 2017, 19, 5868-5871
1547735 CIFC21 H27 N O4P 1 21/c 19.9109; 17.7633; 10.9397
90; 100.598; 90
1893.1Wang, Chengfeng; Lu, Zhan
Intermolecular [2 + 2] Cycloaddition of 1,4-Dihydropyridines with Olefins via Energy Transfer.
Organic letters, 2017, 19, 5888-5891
1547736 CIFC31 H37 N O4P 1 21 17.459; 15.314; 11.5062
90; 91.057; 90
1314.1Wang, Chengfeng; Lu, Zhan
Intermolecular [2 + 2] Cycloaddition of 1,4-Dihydropyridines with Olefins via Energy Transfer.
Organic letters, 2017, 19, 5888-5891
1547737 CIFC27 H31 N O4C 1 c 112.1961; 9.8018; 19.978
90; 97.063; 90
2370.1Wang, Chengfeng; Lu, Zhan
Intermolecular [2 + 2] Cycloaddition of 1,4-Dihydropyridines with Olefins via Energy Transfer.
Organic letters, 2017, 19, 5888-5891
1547738 CIFC21 H27 N O4P 1 21/n 18.5401; 11.6431; 19.9467
90; 98.271; 90
1962.7Wang, Chengfeng; Lu, Zhan
Intermolecular [2 + 2] Cycloaddition of 1,4-Dihydropyridines with Olefins via Energy Transfer.
Organic letters, 2017, 19, 5888-5891
1547739 CIFC17 H14 O5P 21 21 218.3616; 8.7783; 19.3853
90; 90; 90
1422.89Luo, Kui; Cao, Tongxiang; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Gold-Catalyzed Ring Expansion of Enyne-Lactone: Generation and Transformation of 2-Oxoninonium.
Organic letters, 2017, 19, 5856-5859
1547740 CIFC18 H13 F O2P 1 21/c 116.1365; 7.3743; 11.6885
90; 103.14; 90
1354.46Luo, Kui; Cao, Tongxiang; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Gold-Catalyzed Ring Expansion of Enyne-Lactone: Generation and Transformation of 2-Oxoninonium.
Organic letters, 2017, 19, 5856-5859
1547741 CIFC22 H18 O6P -18.6474; 9.0011; 11.6253
92.573; 94.393; 91.114
901.06Luo, Kui; Cao, Tongxiang; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Gold-Catalyzed Ring Expansion of Enyne-Lactone: Generation and Transformation of 2-Oxoninonium.
Organic letters, 2017, 19, 5856-5859
1547742 CIFC25 H23 N O2 SP 1 21/c 114.4968; 10.5034; 15.0275
90; 111.709; 90
2125.9Wen, Jian; Cheng, Hanchao; Raabe, Gerhard; Bolm, Carsten
Rhodium-Catalyzed [4 + 3] Annulations of Sulfoximines with α,β-Unsaturated Ketones Leading to 1,2-Benzothiazepine 1-Oxides.
Organic letters, 2017, 19, 6020-6023
1547760 CIFC43 H29 N3 O3P -17.925; 12.5953; 15.5199
87.325; 87.557; 87.368
1544.57Kumar, Ankit; Rajeswara Rao, M.; Lee, Way-Zen; Ravikanth, Mangalampalli
Hybrid Macrocycles of Subporphyrins and Triphyrins.
Organic letters, 2017, 19, 5924-5927
1547761 CIFC46 H24 F5 O5 Re SC 1 2/c 133.542; 10.9252; 25.824
90; 124.876; 90
7763.6Kumar, Ankit; Rajeswara Rao, M.; Lee, Way-Zen; Ravikanth, Mangalampalli
Hybrid Macrocycles of Subporphyrins and Triphyrins.
Organic letters, 2017, 19, 5924-5927
1547762 CIFC46 H28 N3 O6 ReP -110.5547; 13.5822; 17.121
107.906; 102.148; 104.773
2144.2Kumar, Ankit; Rajeswara Rao, M.; Lee, Way-Zen; Ravikanth, Mangalampalli
Hybrid Macrocycles of Subporphyrins and Triphyrins.
Organic letters, 2017, 19, 5924-5927
1547763 CIFC43 H25 F5 N2 SC 1 2/c 130.947; 10.5971; 22.6459
90; 107.749; 90
7073.2Kumar, Ankit; Rajeswara Rao, M.; Lee, Way-Zen; Ravikanth, Mangalampalli
Hybrid Macrocycles of Subporphyrins and Triphyrins.
Organic letters, 2017, 19, 5924-5927
1547765 CIFC28 H42 F2 N4 O12.5P 1 21 114.578; 13.1698; 19.698
90; 106.053; 90
3634.3Burade, Sachin S.; Saha, Tanmoy; Bhuma, Naresh; Kumbhar, Navanath; Kotmale, Amol; Rajamohanan, Pattuparambil R.; Gonnade, Rajesh G.; Talukdar, Pinaki; Dhavale, Dilip D.
Self-Assembly of Fluorinated Sugar Amino Acid Derived α,γ-Cyclic Peptides into Transmembrane Anion Transport.
Organic letters, 2017, 19, 5948-5951
1547766 CIFC24 H20 Cl0 N2 O5 SP b c a11.3088; 13.4942; 27.4368
90; 90; 90
4186.9Pal, Kuntal; Shukla, Rahul K.; Volla, Chandra M. R.
Rh(II)-Catalyzed Denitrogenative Reaction of N-Sulfonyl-1,2,3-triazoles with Isatins for the Construction of Indigoids.
Organic letters, 2017, 19, 5764-5767
1547781 CIFC21 H21 N3P 1 21 19.6502; 10.1186; 9.806
90; 112.655; 90
883.64Wang, Xu; Xiong, Wenfang; Huang, Yubing; Zhu, Jiayi; Hu, Qiong; Wu, Wanqing; Jiang, Huanfeng
Palladium-Catalyzed Synthesis of 1H-Indenes and Phthalimides via Isocyanide Insertion.
Organic letters, 2017, 19, 5818-5821
1547782 CIFC33 H31 Cl2 N3 O4 S2P -19.974; 14.056; 14.062
83.992; 88.531; 73.514
1880An, Yuanyuan; Wu, Jie
Synthesis of Tetrahydropyridine Derivatives through a Reaction of 1,6-Enynes, Sulfur Dioxide, and Aryldiazonium Tetrafluoroborates.
Organic letters, 2017, 19, 6028-6031
1547783 CIFC27 H29 N3 O4 S2P 1 21 17.9678; 10.943; 15.044
90; 95.755; 90
1305.1An, Yuanyuan; Wu, Jie
Synthesis of Tetrahydropyridine Derivatives through a Reaction of 1,6-Enynes, Sulfur Dioxide, and Aryldiazonium Tetrafluoroborates.
Organic letters, 2017, 19, 6028-6031
1547784 CIFC20 H15 Br N2 O2P 21 21 216.1589; 7.3312; 38.746
90; 90; 90
1749.5Maity, Sanjay; Saha, Mithu; Hazra, Gurupada; Ghorai, Prasanta
Switchable Chemoselectivity for Organocatalytic, Asymmetric Malononitrile Addition to ortho-Formyl Chalcones.
Organic letters, 2017, 19, 5872-5875
1547785 CIFC25 H16 Br F N2 O2P 1 21/c 112.7986; 16.9506; 10.2527
90; 108.443; 90
2110Maity, Sanjay; Saha, Mithu; Hazra, Gurupada; Ghorai, Prasanta
Switchable Chemoselectivity for Organocatalytic, Asymmetric Malononitrile Addition to ortho-Formyl Chalcones.
Organic letters, 2017, 19, 5872-5875
1547786 CIFC24 H21 N3 O2P 1 21/c 112.624; 8.002; 19.474
90; 96.48; 90
1954.64Xia, Jintao; Kong, Lingheng; Zhou, Xukai; Zheng, Guangfan; Li, Xingwei
Access to Substituted Propenoic Acids via Rh(III)-Catalyzed C-H Allylation of (Hetero)Arenes with Methyleneoxetanones.
Organic letters, 2017, 19, 5972-5975
1547787 CIFC23 H19 F3 OP 1 21/n 113.2977; 5.57216; 25.8974
90; 103.075; 90
1869.17Horino, Yoshikazu; Sugata, Miki; Mutsuura, Itaru; Tomohara, Keisuke; Abe, Hitoshi
Controllable Stereoselective Synthesis of (Z)- and (E)-Homoallylic Alcohols Using a Palladium-Catalyzed Three-Component Reaction.
Organic letters, 2017, 19, 5968-5971
1547788 CIFC34 H26 Cl2 Fe N2 OP 1 21/c 115.0345; 7.8241; 24.411
90; 100.874; 90
2819.9Sattar, Moh; Kumar, Sangit
Palladium-Catalyzed Removable 8-Aminoquinoline Assisted Chemo- and Regioselective Oxidative sp(2)-C-H/sp(3)-C-H Cross-Coupling of Ferrocene with Toluene Derivatives.
Organic letters, 2017, 19, 5960-5963
1547789 CIFC44 H48 Fe N2 OP -112.674; 12.6962; 13.5789
68.465; 64.191; 88.015
1809.18Sattar, Moh; Kumar, Sangit
Palladium-Catalyzed Removable 8-Aminoquinoline Assisted Chemo- and Regioselective Oxidative sp(2)-C-H/sp(3)-C-H Cross-Coupling of Ferrocene with Toluene Derivatives.
Organic letters, 2017, 19, 5960-5963
1547790 CIFC34 H26 Fe I2 N2 OP 1 21/n 17.3942; 18.6187; 20.9626
90; 94.192; 90
2878.2Sattar, Moh; Kumar, Sangit
Palladium-Catalyzed Removable 8-Aminoquinoline Assisted Chemo- and Regioselective Oxidative sp(2)-C-H/sp(3)-C-H Cross-Coupling of Ferrocene with Toluene Derivatives.
Organic letters, 2017, 19, 5960-5963
1547791 CIFC26 H22 Br N3 O3P 21 21 219.3208; 12.8006; 19.003
90; 90; 90
2267.28Zhang, Qian; Guo, Songsong; Yang, Jian; Yu, Kunru; Feng, Xiaoming; Lin, Lili; Liu, Xiaohua
Asymmetric Formal [3 + 2]-Cycloaddition of Azomethine Imines with Azlactones To Synthesize Bicyclic Pyrazolidinones.
Organic letters, 2017, 19, 5826-5829
1547800 CIFC27 H23 Cl Fe N2P 21 21 217.3285; 9.4849; 40.0645
90; 90; 90
2784.89Chen, Zhixiong; Han, Lu; Tian, Shi-Kai
Activation and Substitution of 1-Ferrocenylalkylamines with Allenones: Application to Three-Component Synthesis of 4-(1-Ferrocenylalkyl)pyrazoles.
Organic letters, 2017, 19, 5852-5855
1547801 CIFC11 H11 I O2 SeP b c a12.931; 10.477; 18.151
90; 90; 90
2459.1Maity, Pintu; Paroi, Bidisha; Ranu, Brindaban C.
Transition-Metal-Free Iodine Catalyzed Selenocayanation of Styrenyl Bromides and an Easy Access to Benzoselenophenes via Intermediacy of Styrenyl Selenocyanate.
Organic letters, 2017, 19, 5748-5751
1547806 CIFC27 H20 Br F3 O2P 1 21 115.066; 8.9311; 18.428
90; 109.998; 90
2330.1Zhang, Junyou; Wu, Hai-Hong; Zhang, Junliang
Enantioselective Phosphine-Catalyzed Allylic Alkylations of mix-Indene with MBH Carbonates.
Organic letters, 2017, 19, 6080-6083
1547820 CIFC25 H19 N O3P 1 21/c 111.4981; 8.6697; 19.4068
90; 94.782; 90
1927.83Samineni, Ramesh; Madapa, Jaipal; Pabbaraja, Srihari; Mehta, Goverdhan
Stitching Oxindoles and Ynones in a Domino Process: Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B.
Organic letters, 2017, 19, 6152-6155
1547821 CIFC18 H17 N O3C 1 2/c 116.581; 10.7796; 17.25
90; 102.204; 90
3013.5Samineni, Ramesh; Madapa, Jaipal; Pabbaraja, Srihari; Mehta, Goverdhan
Stitching Oxindoles and Ynones in a Domino Process: Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B.
Organic letters, 2017, 19, 6152-6155
1547822 CIFC16 H19 B O4P 1 21/c 16.538; 16.718; 13.471
90; 90.09; 90
1472.4Murai, Masahito; Mizuta, Chisato; Taniguchi, Ryuji; Takai, Kazuhiko
Synthesis of Borylcyclopropanes by Chromium-Promoted Cyclopropanation of Unactivated Alkenes.
Organic letters, 2017, 19, 6104-6107
1547823 CIFC16 H26.5 O7.25I 1 2 119.911; 5.551; 30.35
90; 95.908; 90
3337Hurtak, Jessica A.; McDonald, Frank E.
Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors.
Organic letters, 2017, 19, 6036-6039
1547824 CIFC15 H25 I O5P 21 21 2110.02693; 11.10793; 14.3797
90; 90; 90
1601.59Hurtak, Jessica A.; McDonald, Frank E.
Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors.
Organic letters, 2017, 19, 6036-6039
1547825 CIFC19 H18 O4P 1 21/n 110.697; 9.009; 16.863
90; 106.217; 90
1560.4Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547826 CIFC26 H25 N O5 SP 1 21/c 114.411; 12.274; 13.749
90; 112.87; 90
2240.8Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547827 CIFC24 H27 N O5 SP -19.304; 10.764; 11.843
98.386; 96.739; 109.699
1086.9Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547828 CIFC28 H29 N O6 SP 1 21/n 18.72; 21.854; 13.387
90; 104.956; 90
2464.7Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547829 CIFC22 H22 N2 O8P -19.377; 10.292; 12.467
75.494; 70.702; 64.502
1016.7Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547830 CIFC16 H18 O4P 1 21/n 111.1174; 8.648; 14.313
90; 92.161; 90
1375.1Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547831 CIFC17 H20 O3 SP 1 21/n 110.5546; 22.9756; 13.1098
90; 98.657; 90
3142.9Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547832 CIFC17 H21 N O3P -111.018; 11.202; 12.907
76.79; 79.73; 84.52
1524Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547833 CIFC27 H27 N O5 SP -111.246; 11.3077; 11.3931
86.918; 62.751; 68.161
1183.6Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547834 CIFC24 H29 N O5 SP 1 21/n 111.5447; 17.0612; 12.493
90; 113.393; 90
2258.4Gharpure, Santosh J.; Anuradha, Dandela
Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation.
Organic letters, 2017, 19, 6136-6139
1547841 CIFC23 H24 N2 O5P -110.0991; 10.6816; 11.0208
61.574; 78.04; 87.766
1020.4Xie, Jialin; Huang, Yuanqiong; Song, Hongjian; Liu, Yuxiu; Wang, Qingmin
Copper-Catalyzed Aerobic Oxidative [2 + 3] Cyclization/Aromatization Cascade Reaction: Atom-Economical Access to Tetrasubstituted 4,5-Biscarbonyl Imidazoles.
Organic letters, 2017, 19, 6056-6059
1547842 CIFC37 H32 I N3 O3C 1 2/c 118.8797; 13.6265; 24.4476
90; 94.0494; 90
6273.8Balalaie, Saeed; Mirzaie, Sattar; Nikbakht, Ali; Hamdan, Fatima; Rominger, Frank; Navari, Razieh; Bijanzadeh, Hamid Reza
Indium-Catalyzed Intramolecular Hydroamidation of Alkynes: An Exo-Dig Cyclization for the Synthesis of Pyranoquinolines through Post-Transformational Reaction.
Organic letters, 2017, 19, 6124-6127
1547859 CIFC23 H18 N2 O2 SP -110.817; 11.6749; 16.4638
97.305; 96.365; 108.875
1925.64Modi, Anju; Sau, Prasenjit; Patel, Bhisma K.
Base-Promoted Synthesis of Quinoline-4(1H)-thiones from o-Alkynylanilines and Aroyl Isothiocyanates.
Organic letters, 2017, 19, 6128-6131
1547860 CIFC30.16 H25.33 Cl0.33 N O2P 6526.4511; 26.4511; 11.7055
90; 90; 120
7092.64Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles.
Organic letters, 2017, 19, 6112-6115
1547861 CIFC32 H28 Br2 N2 O4.5C 1 2 123.9252; 10.3277; 12.9767
90; 98.8598; 90
3168.18Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles.
Organic letters, 2017, 19, 6112-6115
1547862 CIFC31 H25 Br2 Cl3 N2 O4P -19.6966; 10.8744; 15.2236
84.4918; 86.8253; 73.5134
1531.48Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles.
Organic letters, 2017, 19, 6112-6115
1547863 CIFC31.5 H27 F2 N2 O4.5C 1 2 124.0915; 9.3008; 12.4495
90; 99.6191; 90
2750.34Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles.
Organic letters, 2017, 19, 6112-6115
1547874 CIFC19 H18 N2 O2 SC 1 2/c 114.3; 8.3251; 29.9248
90; 99.0075; 90
3518.6Ramesh, Balu; Jeganmohan, Masilamani
Ruthenium-Catalyzed Remote C-H Sulfonylation of N-Aryl-2-aminopyridines with Aromatic Sulfonyl Chlorides.
Organic letters, 2017, 19, 6000-6003
1547875 CIFC20 H20 N2 O2 SC 1 2/c 114.8321; 8.4143; 29.8348
90; 97.4759; 90
3691.8Ramesh, Balu; Jeganmohan, Masilamani
Ruthenium-Catalyzed Remote C-H Sulfonylation of N-Aryl-2-aminopyridines with Aromatic Sulfonyl Chlorides.
Organic letters, 2017, 19, 6000-6003
1547876 CIFC15 H14 N4 O4P 1 21/n 18.006; 12.99; 14.7
90; 100.16; 90
1505Mondal, Ramij R.; Khamarui, Saikat; Maiti, Dilip K.
Photocatalytic Generation of Nitrenes for Rapid Diaziridination.
Organic letters, 2017, 19, 5964-5967
1547905 CIFC29 H33 Br O4P -19.8378; 10.0606; 14.0335
70.001; 80.759; 83.195
1285.2Yang, Jun; Xu, Wenbo; Cui, Qi; Fan, Xing; Wang, Lu-Ning; Yu, Zhi-Xiang
Asymmetric Total Synthesis of (-)-Clovan-2,9-dione Using Rh(I)-Catalyzed [3 + 2 + 1] Cycloaddition of 1-Yne-vinylcyclopropane and CO.
Organic letters, 2017, 19, 6040-6043
1547906 CIFC23 H24 O2P 1 21 111.9476; 5.9856; 12.3311
90; 93.344; 90
880.34Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547907 CIFC22 H16 Cl F3P b c a10.6429; 17.14; 19.551
90; 90; 90
3566.5Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547908 CIFC22 H20 Cl F OP 21 21 215.973; 15.888; 18.3194
90; 90; 90
1738.5Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547909 CIFC21 H19 NP 1 21/n 18.6347; 10.9298; 16.4312
90; 93.191; 90
1548.3Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547910 CIFC23 H21 ClP 1 21/c 19.7435; 20.96; 9.8864
90; 113.368; 90
1853.4Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547911 CIFC22 H19 IP 1 21 15.7244; 14.8287; 21.3598
90; 97.293; 90
1798.47Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547912 CIFC23 H23 Cl OP -16.4515; 17.1888; 18.0877
68.737; 87.418; 89.422
1867.33Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547913 CIFC22 H25 N O2P -16.1271; 16.148; 18.8563
90.872; 97.1; 98.775
1828.57Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547914 CIFC22 H21 Cl OP 1 21/c 111.7165; 6.0572; 24.9509
90; 94.48; 90
1765.33Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547915 CIFC23 H24 OP 1 21 15.9827; 25.0699; 11.6168
90; 90.887; 90
1742.14Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547916 CIFC23 H23 Cl OP 1 21/c 118.5748; 6.4645; 15.9299
90; 107.348; 90
1825.8Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547917 CIFC22 H21 I OP 1 21/c 112.1357; 6.0494; 25.0871
90; 96.515; 90
1829.84Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547918 CIFC22 H19 FP -18.9407; 9.6685; 10.3518
113.062; 90.552; 92.535
822.17Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547919 CIFC23 H24 OP 1 21/c 117.524; 5.9716; 16.6106
90; 94.777; 90
1732.2Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547920 CIFC20 H17 Cl SP -18.5228; 12.1509; 17.005
72.107; 89.784; 82.281
1659.36Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547921 CIFC23 H24 O2P 1 21/c 118.524; 5.7934; 16.9793
90; 105.284; 90
1757.7Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547922 CIFC22 H19 FP 1 21/n 110.1038; 8.9144; 18.5125
90; 95.222; 90
1660.5Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547923 CIFC23 H22 OP -19.5851; 9.9859; 10.2722
78.476; 66.039; 75.513
864.54Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547924 CIFC21 H19 NP n a 2113.5127; 9.4159; 25.6168
90; 90; 90
3259.3Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547925 CIFC21 H21 N OP 16.1157; 7.6877; 35.725
88.193; 85.251; 82.371
1658.7Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547926 CIFC27 H30 O3P 1 21/n 117.0051; 7.463; 18.2727
90; 97.403; 90
2299.6Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547927 CIFC23 H21 ClP -19.5964; 9.794; 10.906
99.828; 94.064; 118.202
876.4Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547928 CIFC23 H22P 1 21/c 15.7206; 16.0457; 18.9021
90; 91.033; 90
1734.76Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547929 CIFC37 H38 N O4 PP 1 21/c 110.7335; 14.9683; 20.7298
90; 103.232; 90
3242.1Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547930 CIFC23 H21 Cl OP -15.4926; 9.9685; 18.0281
80.689; 89.091; 74.881
940.01Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547931 CIFC27 H28 O2P 1 21/n 114.358; 9.3991; 16.714
90; 104.03; 90
2188.3Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547932 CIFC22 H21 F OP 1 21 111.7538; 5.9738; 12.1137
90; 93.451; 90
849.02Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547933 CIFC23 H22 OP -18.7067; 9.2287; 12.614
77.052; 72.793; 64.314
867.09Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547934 CIFC20 H19 Cl O SP 21 21 215.737; 15.6229; 18.8695
90; 90; 90
1691.25Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547935 CIFC23 H21 Cl OP 1 21/c 15.8455; 16.6918; 37.3464
90; 90.567; 90
3643.8Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547936 CIFC23 H24 O2P -16.5207; 16.0428; 17.9567
83.358; 86.821; 80.353
1838.2Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547937 CIFC22 H21 F OP 21 21 215.8984; 16.5715; 17.3993
90; 90; 90
1700.7Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547938 CIFC23 H23 Cl O2P -18.2234; 8.767; 13.8661
91.431; 95.956; 110.953
926.45Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547939 CIFC20 H20 O SP 21 21 215.9092; 13.9608; 39.1514
90; 90; 90
3229.9Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547940 CIFC22 H19 ClP 21 21 216.1056; 18.6607; 5.7399
90; 90; 90
1725.08Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1547941 CIFC22 H18 Cl FC 1 2/c 120.898; 10.2307; 17.2114
90; 109.785; 90
3462.6Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis
Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach.
Organic letters, 2017, 19, 6212-6215
1548052 CIFC7 H4 Cl2 O2P -16.6783; 7.8355; 8.1648
65.48; 86.218; 72.786
370.51Chen, Xiao-Yang; Ozturk, Seyma; Sorensen, Erik J.
Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group.
Organic letters, 2017, 19, 6280-6283
1548125 CIFC23 H20 N2 OP -17.7845; 10.4296; 11.802
85.724; 74.803; 69.047
863.35Zhu, Zhengbo; Lv, Xin; Anesini, Jason E.; Seidel, Daniel
Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation.
Organic letters, 2017, 19, 6424-6427
1548126 CIFC29 H24 N2 OP 1 21/c 110.6445; 18.8991; 11.1931
90; 109.71; 90
2119.81Zhu, Zhengbo; Lv, Xin; Anesini, Jason E.; Seidel, Daniel
Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation.
Organic letters, 2017, 19, 6424-6427
1548127 CIFC18 H17 N O4 SC 1 c 113.726; 15.964; 7.7194
90; 111.03; 90
1578.8Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao
Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles.
Organic letters, 2017, 19, 6268-6271
1548128 CIFC18 H17 N O5 SP 1 21/c 16.3553; 14.813; 17.085
90; 95.7; 90
1600.4Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao
Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles.
Organic letters, 2017, 19, 6268-6271
1548129 CIFC18 H17 N O5 SP -16.1967; 11.195; 12.7835
110.691; 92.738; 93.838
825.33Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao
Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles.
Organic letters, 2017, 19, 6268-6271
1548130 CIFC12 H13 N O4 SP 21 21 215.7561; 10.135; 20.636
90; 90; 90
1203.9Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao
Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles.
Organic letters, 2017, 19, 6268-6271
1548606 CIFC18 H18 O5 SP -19.1078; 9.1877; 11.146
81.945; 68.341; 81.982
854.38Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai
Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives.
Organic letters, 2017, 19, 6084-6087
1548607 CIFC24 H26 O7 SP 1 21/n 17.584; 23.96; 13.042
90; 95.24; 90
2360Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai
Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives.
Organic letters, 2017, 19, 6084-6087
1548608 CIFC24 H25 F O7 SP -17.7157; 11.4525; 13.9009
97.178; 95.839; 100.355
1189.1Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai
Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives.
Organic letters, 2017, 19, 6084-6087
1548609 CIFC24 H21 Cl O5 SP -18.68; 10.624; 12.798
79.965; 74.188; 89.59
1117.1Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai
Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives.
Organic letters, 2017, 19, 6084-6087
1548610 CIFC17 H14 O S2P 1 21/c 19.5414; 17.3999; 9.7984
90; 116.714; 90
1453.1Wang, Quannan; Yang, Xiaoge; Wu, Ping; Yu, Zhengkun
Photoredox-Catalyzed C-H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen.
Organic letters, 2017, 19, 6248-6251
1548611 CIFC17 H13 N3 O3 S2P 1 21/n 14.0165; 23.916; 17.104
90; 94.419; 90
1638.1Wang, Quannan; Yang, Xiaoge; Wu, Ping; Yu, Zhengkun
Photoredox-Catalyzed C-H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen.
Organic letters, 2017, 19, 6248-6251
1548612 CIFC19 H17 Br N2 O2P 21 21 216.2066; 16.3879; 16.6057
90; 90; 90
1689Yuan, Shiru; Luo, Yuchen; Peng, Jingyi; Miao, Maozhong; Xu, Jianfeng; Ren, Hongjun
Oxidative Asymmetric [2 + 3] Annulation of Aldehydes with Azomethine Imines Enabled by N-Heterocyclic Carbene Catalysis.
Organic letters, 2017, 19, 6100-6103
1554753 CIFC31 H26 Cl N O4P 21 21 217.9152; 11.4088; 28.388
90; 90; 90
2563.5He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang
Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight.
Organic letters, 2015, 17, 1365-1368
1554755 CIFC22 H25 O5 PP -17.8931; 9.4542; 14.3399
89.1605; 82.9814; 69.4905
994.29Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho
Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins.
Organic letters, 2015, 17, 908-911
1554756 CIFC26 H23 B F4 N2 O2P 1 21/c 112.2068; 13.731; 14.626
90; 99.027; 90
2421.1Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554764 CIFC25 H20 B F4 N OP 1 21/n 110.72; 18.331; 12.174
90; 110.527; 90
2240.4Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554765 CIFC25 H21 B F4 N2 O2P 1 21/c 112.3471; 13.3272; 13.9786
90; 98.588; 90
2274.42Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554767 CIFC31 H24 Cl N O3P 1 21 17.081; 19.406; 9.491
90; 98.161; 90
1290.99Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy
Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles.
Organic letters, 2015, 17, 1066-1069
1554773 CIFC49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2P -110.3083; 14.3567; 19.2355
75.287; 74.747; 84.913
2655.7Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554774 CIFC16 H19 Cl3 N P TiP -18.8951; 9.2936; 13.0036
79.226; 76.069; 64.74
939.24Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554776 CIFC35 H26 N1.6 O10P 21 21 2113.871; 15.1622; 64.627
90; 90; 90
13592Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong
New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family.
Organic letters, 2015, 17, 1146-1149
1554782 CIFC34 H29 N5 O4 SP -19.7972; 10.509; 15.4371
72.931; 74.564; 84.268
1464.2Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang
Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles.
Organic letters, 2015, 17, 1192-1195
1554783 CIFC24 H27 N3 O2P 1 21/c 117.5333; 9.245; 13.3467
90; 107.946; 90
2058.18Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554791 CIFC21 H15 N3 OP 1 21/c 110.5706; 17.3802; 10.1316
90; 96.996; 90
1847.5Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554793 CIFC24 H21 I N2 O3 SP 21 21 2110.7482; 12.7229; 16.152
90; 90; 90
2208.76Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas.
Organic letters, 2015, 17, 1018-1021
1554794 CIFC19 H24 N2 OP c a 2112.8993; 10.853; 11.6466
90; 90; 90
1630.5Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng
Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond.
Organic letters, 2015, 17, 1200-1203
1554796 CIFC24 H44 B2 N2 O4P b a m12.939; 13.093; 15.573
90; 90; 90
2638.2Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554797 CIFC29 H49 B2 Co N2 O4F d d 218.923; 58.36; 11.127
90; 90; 90
12288Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554798 CIFC24 H46 B2 N2 O5P 1 21/n 110.74; 19.626; 13.066
90; 93.197; 90
2749.8Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554802 CIFC24 H41 B2 O2 PP 1 21/n 18.6014; 17.6656; 16.4517
90; 107.162; 90
2388.51Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554803 CIFC28 H33 B2 Fe O2 PP 1 21 112.674; 9.2986; 12.919
90; 113.497; 90
1396.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554804 CIFC40 H43 B2 Fe PP 21 21 2110.3874; 17.4963; 18.3521
90; 90; 90
3335.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554806 CIFC13 H12 O4P 1 21/n 110.5408; 14.0223; 15.567
90; 95.216; 90
2291.4Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan
Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates.
Organic letters, 2015, 17, 1228-1231
1554809 CIFC19 H18 N O5 S2P -17.9459; 8.3713; 15.0845
98.477; 91.135; 97.754
982.54Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan
Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.
Organic letters, 2015, 17, 1834-1837
1554810 CIFC24 H22 O3C 1 c 114.8194; 23.1341; 17.3079
90; 104.994; 90
5731.7Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc
Development of a new family of chiral auxiliaries.
Organic letters, 2015, 17, 1819-1821
1554813 CIFC17 H16 Cl N3 OP -18.6811; 13.1015; 15.2298
66.74; 82.416; 77.876
1553.57Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping
One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides.
Organic letters, 2015, 17, 1157-1159
1554814 CIFC34 H35 N O6 SP 21 21 219.4387; 22.551; 28.131
90; 90; 90
5987.7Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R.
2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors.
Organic letters, 2015, 17, 1421-1424
1554815 CIFC19 H21 F2 N OP 1 21/c 19.9286; 17.0093; 10.0841
90; 90.259; 90
1703He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo
Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates.
Organic letters, 2015, 17, 1838-1841
1554822 CIFC16 H10 N2 OP 1 21/n 16.4176; 20.0965; 9.335
90; 98.274; 90
1191.42Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie
Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles.
Organic letters, 2015, 17, 1445-1448
1554824 CIFC20 H14 O5P 1 21/n 19.0391; 9.7069; 17.2285
90; 102.573; 90
1475.41Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang
Muta-mycosynthesis of naphthalene analogs.
Organic letters, 2015, 17, 1457-1460
1554830 CIFC20 H25 F3 N2 O3 SP 1 21/c 18.128; 15.344; 16.979
90; 102.44; 90
2067.8van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554831 CIFC22 H30 F3 N3 O3 SC 1 2/c 115.441; 10.924; 27.769
90; 90.9; 90
4683.4van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554832 CIFC18 H22 F3 N3 O3 SP 1 21/c 18.4815; 11.074; 21.3223
90; 93.426; 90
1999.1van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554833 CIFC21 H25 N3P -18.61; 9.179; 11.835
93.38; 95.73; 105.2
894.57van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554834 CIFC20 H26 N2P 1 21/c 18.693; 17.464; 11.525
90; 103.69; 90
1700van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554835 CIFC14 H22 N2R 3 c :H26.3163; 26.3163; 10.403
90; 90; 120
6239.3van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554837 CIFC49 H29 B F20 N O2 RhP 1 21/c 112.2787; 24.2002; 15.5541
90; 101.818; 90
4523.9Otley, Kate D.; Ellman, Jonathan A.
An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation.
Organic letters, 2015, 17, 1332-1335
1554838 CIFC18 H18 O2P 1 21/c 114.026; 8.7035; 12.0599
90; 104.008; 90
1428.4Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin
Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process.
Organic letters, 2015, 17, 1489-1492
1554839 CIFC17 H16 O2 SeP 1 21 16.9078; 10.3981; 10.0732
90; 95.471; 90
720.24Niu, Wenxue; Yeung, Ying-Yeung
Catalytic and highly enantioselective selenolactonization.
Organic letters, 2015, 17, 1660-1663
1554840 CIFC12 H20 O4P 3213.594; 13.594; 5.7493
90; 90; 120
920.11Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John
Exo-selective reductive macrocyclization of ynals.
Organic letters, 2015, 17, 1493-1496
1554841 CIFC14 H15 Br N2 O2P 21 21 219.2455; 10.1411; 14.412
90; 90; 90
1351.3Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing
A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters.
Organic letters, 2015, 17, 1505-1508
1554842 CIFC22 H18 F N3 O2 SP 1 21/c 115.7629; 11.6907; 10.7408
90; 100.958; 90
1943.22Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554855 CIFC18 H21 N3 O2 S2P 1 21/c 110.0095; 11.563; 16.5773
90; 99.859; 90
1890.32Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554856 CIFC20 H26 N2 O8 SiC 1 2/c 118.687; 6.709; 37.603
90; 90.534; 90
4714Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei
Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal.
Organic letters, 2015, 17, 1553-1556
1554858 CIFC60 H85 I3 N10 O12P -114.2686; 14.6629; 17.0163
80.443; 70.781; 82.037
3301.6Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554860 CIFC60 H78 Cl6 N10 O10C 1 2/c 122.9779; 30.564; 22.926
90; 114.207; 90
14685.1Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554862 CIFC27 H27 F3 N2 O8P -18.5362; 11.0883; 14.8339
89.337; 75.808; 89.011
1360.96Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan
Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes.
Organic letters, 2015, 17, 1589-1592
1554864 CIFC14 H11 N O7P n a 218.6933; 19.9383; 7.6281
90; 90; 90
1322.18Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study.
Organic letters, 2015, 17, 1850-1853
1554867 CIFC23 H26 Br N O4 SP 1 21 19.8067; 9.9678; 11.8916
90; 104.237; 90
1126.7Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization.
Organic letters, 2015, 17, 1720-1723
1554869 CIFC28 H19 N O3 S2P -110.443; 11.228; 11.795
70.186; 87.728; 65.484
1175.6Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang
Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes.
Organic letters, 2015, 17, 1746-1749
1554871 CIFC15 H21 N O3P 1 21/n 15.1627; 14.8595; 17.7219
90; 96.198; 90
1351.59Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron
Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids.
Organic letters, 2015, 17, 1754-1757
1554873 CIFC20 H16 O2P 21 21 215.9724; 14.8969; 16.4863
90; 90; 90
1466.79Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts.
Organic letters, 2015, 17, 1735-1737
1554875 CIFC12 H13 Br O2P 1 21/c 16.0066; 11.7969; 16.772
90; 97.594; 90
1178Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554877 CIFC23 H21 NP 1 21/c 110.4176; 11.9596; 16.0413
90; 114.231; 90
1822.51Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554878 CIFC29 H36 N2 O4P 1 21 18.527; 16.7982; 9.3056
90; 102.717; 90
1300.22Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554880 CIFC13 H22 O2C 1 c 114.0887; 10.5929; 9.0247
90; 114.771; 90
1222.92Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554885 CIFC20 H20 Br2 Cl2 N2 O4P 15.0746; 14.828; 16.699
65.191; 89.579; 80.838
1123.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554887 CIFC13 H15 Br Cl N O3P 1 21 14.8035; 8.2644; 18.363
90; 94.441; 90
726.79Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554890 CIFC13 H16 Br Cl2 N O3P 1 21 110.669; 4.7706; 15.964
90; 107.952; 90
773Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554894 CIFC6 H12 Cl2 O2P 1 21 14.9886; 19.578; 9.0155
90; 92.03; 90
880Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554896 CIFC13 H15 Br Cl N O3P 1 21 112.2792; 4.9357; 13.4763
90; 115.38; 90
737.92Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554898 CIFC13 H15 Br Cl N O3C 1 2 116.929; 4.841; 36.446
90; 101.211; 90
2930Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554900 CIFC14 H18 Cl N O8 SP 21 21 216.1403; 13.657; 20.719
90; 90; 90
1737.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554902 CIFC6 H12 Cl2 O2P 21 21 215.8932; 9.8358; 14.7998
90; 90; 90
857.86Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554904 CIFC18 H14 N2 OP 1 21/c 117.283; 5.72; 16.0086
90; 115.367; 90
1430Bunescu, Ala; Wang, Qian; Zhu, Jieping
Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles.
Organic letters, 2015, 17, 1890-1893
1554907 CIFC28 H36 N2 O10 Pd3P 1 21/c 18.2684; 13.1049; 14.9823
90; 98.209; 90
1606.8Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng
Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle.
Organic letters, 2015, 17, 1802-1805
1554909 CIFC21 H24 B N O2P 1 21/n 19.82013; 15.1033; 12.9881
90; 93.8267; 90
1922.05Pareek, Manish; Fallon, Thomas; Oestreich, Martin
Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 2082-2085
1554912 CIFC20 H41 B2 F8 N5 OP 21 21 219.9728; 10.8425; 25.575
90; 90; 90
2765.4Mirabdolbaghi, Roya; Dudding, Travis
Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination.
Organic letters, 2015, 17, 1930-1933
1554914 CIFC25 H36 F3 N3 O4P -17.9555; 12.7291; 14.1773
101.894; 105.578; 101.34
1304Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554915 CIFC20 H27 F3 N2 O3P 1 21/c 19.676; 6.0187; 35.338
90; 90.313; 90
2057.9Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554916 CIFC18 H23 F3 N2 O3P -18.4082; 8.9935; 12.6932
109.241; 90.111; 102.16
883.25Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554917 CIFC18 H16 F3 N OP 21 21 215.8836; 19.2027; 26.5181
90; 90; 90
2996Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554920 CIFC21 H16 N2 O2 SC 1 c 113.529; 16.7566; 8.6938
90; 116.175; 90
1768.8Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554921 CIFC24 H24 N2 O2 SP 1 21/c 112.5268; 10.8502; 16.3904
90; 103.482; 90
2166.4Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554924 CIFC19 H29 F N2 O5 SiP 21 21 216.42; 8.0707; 40.1927
90; 90; 90
2082.54Istrate, Alena; Medvecky, Michal; Leumann, Christian J.
2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity.
Organic letters, 2015, 17, 1950-1953
1554926 CIFC19 H16 N2 O4P 1 21 17.5248; 11.7969; 18.7512
90; 98.035; 90
1648.2Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K.
An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence.
Organic letters, 2015, 17, 2102-2105
1554930 CIFC16 H25 N O2 S3P 21 21 215.36225; 12.0412; 27.5363
90; 90; 90
1777.96Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554932 CIFC18 H19 Cl F3 N O SP 1 21 111.7646; 15.4251; 12.0356
90; 118.452; 90
1920.3Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554934 CIFC19 H23 Fe N O2 SP 1 21 15.84461; 11.3132; 13.829
90; 95.4227; 90
910.298Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554935 CIFC23 H17 Cl O2P 1 21/m 19.353; 7.448; 12.251
90; 93.725; 90
851.6Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong
Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones.
Organic letters, 2015, 17, 2134-2137
1554937 CIFC133 H116 N8 O21 S4P 1 21 110.8299; 17.8426; 16.7462
90; 105.418; 90
3119.5Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu
Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.
Organic letters, 2015, 17, 2318-2321
1554941 CIFC39 H30 Cl N OP 1 21/n 114.7817; 10.4931; 20.1054
90; 110.04; 90
2929.66Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554944 CIFC24 H24 Cl N OP 1 21/n 112.0241; 10.8634; 15.0306
90; 92.829; 90
1960.94Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554948 CIFC24 H24 Cl N OP 1 21/c 116.3879; 7.0026; 17.8667
90; 103.718; 90
1991.86Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554950 CIFC152.5 H199 B4 N7 O23P 1 21/c 111.705; 28.512; 22.406
90; 98.94; 90
7387Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554955 CIFC50 H44 F24 N4 P4P 1 21/n 113.488; 14.281; 14.287
90; 108.36; 90
2611.9Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554956 CIFC186 H168 B4 N14 O31P -116.134; 16.609; 16.766
85.82; 65.15; 75.26
3939.7Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554959 CIFC117 H171 B4 N4 O20P 1 21/c 142.193; 8.356; 15.63
90; 90.76; 90
5510.1Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554960 CIFC180 H112 B4 D84 N4 O34 S14P -116.67; 17.44; 19.659
81.21; 74.06; 62.19
4859Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554968 CIFC70 H56 N8 O8P -111.446; 13.451; 22.036
98.71; 104.3; 98.36
3189.9Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554969 CIFC32 H26 N4 O2C 1 2/c 116.098; 8.0852; 19.417
90; 103.12; 90
2461.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554971 CIFC34 H30 N4 O4P 1 21/c 17.3964; 23.302; 16.073
90; 94.05; 90
2763.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554973 CIFC70 H58 Cl6 N8 O12 SC 1 c 137.78; 8.9173; 26.953
90; 133.41; 90
6596Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554978 CIFC16 H10 Br N O4P 1 21/c 112.4447; 15.6502; 7.9646
90; 105.739; 90
1493Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam
Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides.
Organic letters, 2015, 17, 2010-2013
1554981 CIFC70 H120 N14 O26 S8P -113.0106; 13.1402; 14.3888
80.344; 63.999; 78.993
2160.42Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554982 CIFC30 H60 N12 O16 S4C 1 2/c 113.4741; 14.6965; 22.6791
90; 92.704; 90
4485.96Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554988 CIFC40 H69.97 N4 O14 S4P -111.2634; 15.966; 16.009
111.587; 100.691; 109.004
2373.6Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554990 CIFC15 H13 N O4 SP 21 21 218.1609; 9.0398; 19.318
90; 90; 90
1425.1Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping
Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions.
Organic letters, 2015, 17, 2022-2025
1554994 CIFC28 H23 N3 O4 SP 1 21/n 112.8623; 11.3355; 16.9579
90; 94.493; 90
2464.87Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei
Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines.
Organic letters, 2015, 17, 2214-2217
1554996 CIFC19 H22 O7P 1 21/n 16.0808; 23.3393; 12.5225
90; 94.028; 90
1772.82Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2338-2341
1554998 CIFC26 H31 Br N2 O3P -19.6121; 11.761; 13.648
98.331; 109.571; 113.637
1260.2Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu
Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts.
Organic letters, 2015, 17, 2234-2237
1555000 CIFC38 H44 B2 F4 N4 O6P -19.7881; 13.2333; 16.5195
67.596; 77.669; 72.069
1870.86Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond
Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts.
Organic letters, 2015, 17, 2246-2249
1555003 CIFC27 H30 F N O2P -19.3088; 9.5092; 14.5742
92.724; 104.673; 110
1159.92Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555004 CIFC28 H32 F N O2P 21 21 218.03153; 10.686; 28.3689
90; 90; 90
2434.76Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555005 CIFC28 H32 N4 O2P 32 2 111.32263; 11.32263; 35.383
90; 90; 120
3928.44Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555006 CIFC30 H35 N O4P 19.7073; 10.168; 14.0374
85.597; 85.998; 82.306
1366.53Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555007 CIFC28 H31 F2 N O2P 110.4764; 10.6867; 12.3768
85.757; 70.552; 69.477
1222.26Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555008 CIFC28 H31 F2 N O2P 1 21 17.90952; 16.3522; 9.53794
90; 95.6737; 90
1227.58Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555011 CIFC23 H27 Br N2 O5P 1 21/n 18.3956; 11.6027; 23.715
90; 91.1454; 90
2309.7Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri
PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines.
Organic letters, 2015, 17, 2416-2419
1555012 CIFC8 H11 F3 N2 O SP 1 21/c 18.4044; 11.3774; 11.5451
90; 96.16; 90
1097.6Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng
Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates.
Organic letters, 2015, 17, 2438-2441
1555018 CIFC76 H112 F14 N4 Sn4P -110.7975; 11.121; 17.986
82.945; 76.059; 70.925
1978.74Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555019 CIFC32 H4 F26 N4P -16.15317; 9.3804; 13.8177
103.878; 100.265; 98.23
747.31Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555021 CIFC19 H18 O2P n a 2112.91; 9.664; 12.157
90; 90; 90
1516.7Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555022 CIFC17 H22 O2P 21 21 218.6511; 11.009; 15.784
90; 90; 90
1503.3Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555026 CIFC22 H21 N O3P -19.724; 10.178; 10.676
62.165; 79.328; 69.089
872.6Capreti, Naylil M. R.; Jurberg, Igor D.
Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds.
Organic letters, 2015, 17, 2490-2493
1555028 CIFC15 H13 N OR -3 :H26.4383; 26.4383; 8.6956
90; 90; 120
5263.8Zhang, Yan; Wang, Dahai; Cui, Sunliang
Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines.
Organic letters, 2015, 17, 2494-2497
1555031 CIFC36 H39 N O2P 1 21/c 114.8225; 11.0736; 18.657
90; 100.056; 90
3015.3Reddy, Virsinha; Vijaya Anand, Ramasamy
Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.
Organic letters, 2015, 17, 3390-3393
1555034 CIFC25 H27 Fe N O3 SP 1 21 115.0789; 8.6357; 18.2167
90; 106.122; 90
2278.8Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro
Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library.
Organic letters, 2015, 17, 2286-2289
1555037 CIFC17 H14 N2 O3P 1 21/c 18.9224; 9.3813; 18.2533
90; 103.064; 90
1488.32Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho
Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid.
Organic letters, 2015, 17, 2518-2521
1555039 CIFC26 H28 O5P -110.896; 11.118; 11.442
109.812; 100.766; 111.223
1137.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555041 CIFC23 H24 O3P -18.428; 11.011; 11.459
65.415; 87.993; 89.668
966.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555044 CIFC21 H36 O4 SiC 1 2 122.265; 7.7011; 12.8529
90; 102.095; 90
2154.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555045 CIFC12 H14 O3P 1 21/c 112.324; 7.8713; 10.6532
90; 92.217; 90
1032.65Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555051 CIFC36 H55 N O7 Si2P -18.9128; 10.9914; 20.184
91.339; 96.624; 104.357
1899.99Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555052 CIFC15 H20 O5P 21 21 217.3936; 10.5735; 17.817
90; 90; 90
1392.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555053 CIFC21 H38 O5 SP 1 21/c 116.4753; 10.1532; 13.8282
90; 98.669; 90
2286.71Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555059 CIFC15 H22 O6P 1 21/n 18.5281; 18.7862; 9.5185
90; 100.368; 90
1500.07Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489

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