Crystallography Open Database
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Searching journal of publication like 'Organic Letters'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1556002 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 12.7136; 19.6481; 10.0368 90; 104.806; 90 | 2423.9 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556003 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 8.088; 29.039; 10.3957 90; 98.253; 90 | 2416.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556004 | CIF | C28 H26 N2 O3 | P -1 | 9.715; 11.622; 13.28 64.317; 86.248; 74.246 | 1298.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556005 | CIF | C26 H30 N2 O3 | P 1 21/c 1 | 11.5919; 14.5845; 13.8674 90; 97.872; 90 | 2322.4 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556006 | CIF | C34 H36 Cl2 N2 O5 | P 1 21/c 1 | 10.3241; 23.365; 13.7004 90; 99.642; 90 | 3258.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556007 | CIF | C33 H34 N2 O5 | P 1 21/c 1 | 13.9135; 11.8443; 18.4125 90; 108.518; 90 | 2877.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556008 | CIF | C29.5 H29 Cl N2 O3 S | P 32 2 1 | 18.4813; 18.4813; 16.4257 90; 90; 120 | 4858.7 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556009 | CIF | C26 H30 N2 O3 | P 1 21/n 1 | 9.5688; 10.3956; 23.8948 90; 96.847; 90 | 2359.9 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556010 | CIF | C24 H24 N2 O2 | P 1 21/c 1 | 10.9969; 11.8906; 15.8497 90; 106.796; 90 | 1984.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556011 | CIF | C33 H34 N2 O5 | P 1 21/c 1 | 16.2583; 8.9359; 19.545 90; 95.231; 90 | 2827.7 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556012 | CIF | C26 H30 N2 O3 | P 1 21/c 1 | 15.2433; 10.1136; 14.943 90; 94.937; 90 | 2295.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556013 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 7.8226; 30.639; 10.1141 90; 98.682; 90 | 2396.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556014 | CIF | C29 H28 N2 O3 S | P 1 21/c 1 | 8.6571; 29.45; 10.2183 90; 98.7924; 90 | 2574.56 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556015 | CIF | C26 H30 N2 O3 | C 1 2/c 1 | 17.3068; 12.0144; 22.5999 90; 96.044; 90 | 4673.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556016 | CIF | C29 H28 N2 O3 | C 1 2 1 | 22.49; 5.1816; 20.19 90; 90.78; 90 | 2352.6 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556017 | CIF | C29 H28 N2 O3 S | P 1 21/n 1 | 19.7344; 12.7882; 20.279 90; 97.031; 90 | 5079.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
| 1556018 | CIF | C23 H17 Cl O3 | C 1 2 1 | 20.5553; 9.5675; 22.2196 90; 115.687; 90 | 3937.9 | Infante, Rebeca; Martin-Alvarez, Jose M; Andrés, Celia; Nieto, Javier Dimethylzinc-Mediated Addition of Phenylacetylene to α-Diketones Catalyzed by Chiral Perhydro-1,3-benzoxazines. Organic letters, 2017, 19, 1516-1519 |
| 1556019 | CIF | C16 H11 F N2 O | P 21 21 21 | 8.4334; 9.1934; 16.9142 90; 90; 90 | 1311.4 | Jin, Yushu; Chen, Ming; Ge, Shaozhong; Hartwig, John F. Palladium-Catalyzed, Enantioselective α-Arylation of α-Fluorooxindoles. Organic letters, 2017, 19, 1390-1393 |
| 1556020 | CIF | C15 H12 N2 O | P 1 21/n 1 | 16.4017; 7.1335; 20.0858 90; 95.665; 90 | 2338.6 | Yin, Kun; Zhang, Ronghua Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature. Organic letters, 2017, 19, 1530-1533 |
| 1556021 | CIF | C16 H14 N2 O | P n a 21 | 9.9288; 26.7988; 4.7384 90; 90; 90 | 1260.79 | Yin, Kun; Zhang, Ronghua Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature. Organic letters, 2017, 19, 1530-1533 |
| 1556022 | CIF | C17 H13 N O | P 1 21/c 1 | 4.0198; 13.908; 23.21 90; 94.2; 90 | 1294.1 | Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines. Organic letters, 2017, 19, 1550-1553 |
| 1556023 | CIF | C11 H13 N S2 | P 1 21 1 | 9.9321; 22.705; 19.824 90; 98.538; 90 | 4420.9 | Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines. Organic letters, 2017, 19, 1550-1553 |
| 1556024 | CIF | C43 H30 N2 O2 | P -1 | 10.4789; 12.074; 12.5011 92.552; 94.697; 98.319 | 1557.2 | Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions. Organic letters, 2017, 19, 1658-1661 |
| 1556025 | CIF | C42 H28 N2 O2 | P b c a | 18.5446; 17.7946; 18.9442 90; 90; 90 | 6251.5 | Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions. Organic letters, 2017, 19, 1658-1661 |
| 1556026 | CIF | C47 H36 Cl2 N4 O S Zn | P -1 | 11.0032; 12.6313; 14.724 98.868; 96.16; 102.84 | 1950 | Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality. Organic letters, 2017, 19, 1722-1725 |
| 1556027 | CIF | C51 H37 N5 O S Zn | P 1 | 10.6689; 10.8762; 18.2817 83.457; 84.152; 77.519 | 2051.2 | Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality. Organic letters, 2017, 19, 1722-1725 |
| 1556028 | CIF | C32 H27 Br O2 | P 1 21 1 | 9.624; 31.096; 13.229 90; 91.141; 90 | 3958 | Perveen, Saima; Zhao, Zhifei; Zhang, Guoxiang; Liu, Jian; Anwar, Muhammad; Fang, Xinqiang Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Organic letters, 2017, 19, 2470-2473 |
| 1556029 | CIF | C94 H64 O2 | P -1 | 9.9734; 11.3386; 15.3837 79.9686; 85.4756; 79.5603 | 1682.69 | Vadehra, Geeta S.; Jiang, Xing; Dotson, Jordan J.; Chu, Gong M.; Garcia-Garibay, Miguel A High-Yielding and Divergent Paradigm for the Synthesis of D<sub>2h</sub>-Symmetric Octakis-Substituted Pentiptycenequinones. Organic letters, 2017, 19, 1838-1841 |
| 1556030 | CIF | C24 H26 N2 O6 | P 1 21 1 | 11.0167; 8.4713; 13.145 90; 112.969; 90 | 1129.5 | Ran, Guang-Yao; Gong, Ming; Yue, Jing-Fei; Yang, Xing-Xing; Zhou, Su-Lan; Du, Wei; Chen, Ying-Chun Asymmetric Cascade Assembly of 1,2-Diaza-1,3-dienes and α,β-Unsaturated Aldehydes via Dienamine Activation. Organic letters, 2017, 19, 1874-1877 |
| 1556031 | CIF | C14 H9 N O3 S | P 1 21/c 1 | 12.0277; 13.0209; 8.1447 90; 106.121; 90 | 1225.4 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
| 1556032 | CIF | C14 H13 N O3 S | P 21 21 21 | 7.4865; 10.7242; 32.3467 90; 90; 90 | 2597.01 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
| 1556033 | CIF | C14 H12 N O3 S | P 21 21 21 | 9.4952; 13.78766; 23.3234 90; 90; 90 | 3053.42 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
| 1556034 | CIF | C24 H24 N2 O3 Se | P 1 21/c 1 | 9.4838; 10.5004; 21.1264 90; 90.868; 90 | 2103.6 | Foley, Christopher; Shaw, Arthur; Hulme, Christopher Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles. Organic letters, 2017, 19, 2238-2241 |
| 1556035 | CIF | C14 H16 N4 O | P 1 21/m 1 | 7.7378; 6.7075; 12.6395 90; 102.323; 90 | 640.89 | Foley, Christopher; Shaw, Arthur; Hulme, Christopher Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles. Organic letters, 2017, 19, 2238-2241 |
| 1556036 | CIF | C28 H44 Cl2 N8 Ni O2 | I m -3 m | 17.0714; 17.0714; 17.0714 90; 90; 90 | 4975.2 | Zhang, Xingjie; Xia, Aiyou; Chen, Haoyi; Liu, Yuanhong General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)<sub>2</sub>: Key Roles of DMAP. Organic letters, 2017, 19, 2118-2121 |
| 1556037 | CIF | C23 H18 O2 | P 1 21 1 | 6.0965; 7.8294; 17.9271 90; 96.951; 90 | 849.41 | Zhang, Jingfang; Tang, Yuhai; Wei, Wen; Wu, Yong; Li, Yang; Zhang, Junjie; Zheng, Yuansuo; Xu, Silong Organocatalytic Cloke-Wilson Rearrangement: DABCO-Catalyzed Ring Expansion of Cyclopropyl Ketones to 2,3-Dihydrofurans. Organic letters, 2017, 19, 3043-3046 |
| 1556038 | CIF | C26 H34 O4 Si | P 21 21 21 | 9.47; 15.075; 17.824 90; 90; 90 | 2544.6 | Han, Man-Yi; Xie, Xiaoyu; Zhou, Di; Li, Pinhua; Wang, Lei Organocatalyzed Direct Aldol Reaction of Silyl Glyoxylates for the Synthesis of α-Hydroxysilanes. Organic letters, 2017, 19, 2282-2285 |
| 1556039 | CIF | C16 H13 Br F3 N O3 | P 21 21 21 | 5.8132; 8.851; 31.166 90; 90; 90 | 1603.6 | Wang, Pei; Li, Hong-Feng; Zhao, Jia-Zhen; Du, Zhi-Hong; Da, Chao-Shan Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones. Organic letters, 2017, 19, 2634-2637 |
| 1556040 | CIF | C22 H26 O4 S | P b c a | 5.5413; 15.8031; 45.3572 90; 90; 90 | 3971.92 | Zhurakovskyi, Oleksandr; Ellis, Sam R.; Thompson, Amber L.; Robertson, Jeremy Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland-Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl. Organic letters, 2017, 19, 2174-2177 |
| 1556041 | CIF | C19 H37 Br Cu N3 P2 | I 41 c d | 31.5316; 31.5316; 18.8701 90; 90; 90 | 18761.4 | Mastalir, Matthias; Pittenauer, Ernst; Stöger, Berthold; Allmaier, Günter; Kirchner, Karl Three Different Reactions, One Catalyst: A Cu(I) PNP Pincer Complex as Catalyst for C-C and C-N Cross-Couplings. Organic letters, 2017, 19, 2178-2181 |
| 1556042 | CIF | C27 H22 O S | P 21 21 21 | 5.3756; 8.23448; 44.3104 90; 90; 90 | 1961.41 | Wang, Zhaobin; Sun, Jianwei Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes. Organic letters, 2017, 19, 2334-2337 |
| 1556043 | CIF | C11 H10 F7 N3 O2 | P 1 21/c 1 | 16.1302; 7.5328; 12.1195 90; 90.161; 90 | 1472.6 | Wang, Rui; Guan, Wei; Han, Zheng-Bo; Liang, Fushun; Suga, Takeo; Bi, Xihe; Nishide, Hiroyuki Ambient-Light-Promoted Three-Component Annulation: Synthesis of Perfluoroalkylated Pyrimidines. Organic letters, 2017, 19, 2358-2361 |
| 1556044 | CIF | C25 H31 N O7 Si | P -1 | 9.5604; 11.3393; 12.5938 64.094; 79.058; 86.136 | 1205.56 | Parsons, Philip J.; Jones, Daniel R.; Walsh, Lee J.; Allen, Lewis A. T.; Onwubiko, Ada; Preece, Lewis; Board, Johnathan; White, Andrew J. P. An Approach to the Core of Lactonamycin. Organic letters, 2017, 19, 2533-2535 |
| 1556045 | CIF | C19 H20 O3 | C 1 2 1 | 17.9303; 6.8625; 13.4226 90; 99.456; 90 | 1629.16 | Iwamoto, Hiroaki; Akiyama, Sota; Hayama, Keiichi; Ito, Hajime Copper(I)-Catalyzed Stereo- and Chemoselective Borylative Radical Cyclization of Alkyl Halides Bearing an Alkene Moiety. Organic letters, 2017, 19, 2614-2617 |
| 1556046 | CIF | C12 H6 O S2 | P b c a | 5.541; 15.387; 22.574 90; 90; 90 | 1925 | Mitsudo, Koichi; Kurimoto, Yuji; Mandai, Hiroki; Suga, Seiji Synthesis of 3-Benzo[b]thienyl 3-Thienyl Ether via an Addition-Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its π-Extended Derivatives. Organic letters, 2017, 19, 2821-2824 |
| 1556047 | CIF | C19 H26 Cl N2 O Rh | P b c a | 8.0471; 16.3426; 29.6614 90; 90; 90 | 3900.8 | Long, Zhen; Yang, Yudong; You, Jingsong Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles. Organic letters, 2017, 19, 2781-2784 |
| 1556048 | CIF | C22 H24 Cl N2 O Rh | P 1 21/n 1 | 7.58618; 16.9757; 15.6843 90; 93.0656; 90 | 2016.94 | Long, Zhen; Yang, Yudong; You, Jingsong Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles. Organic letters, 2017, 19, 2781-2784 |
| 1556049 | CIF | C116 H112 Cl2 N10 Ni | P -1 | 12.6554; 19.7134; 21.0374 72.334; 80.809; 82.734 | 4919.7 | Yin, Bangshao; Kim, Taeyeon; Zhou, Mingbo; Huang, Weiming; Kim, Dongho; Song, Jianxin Porphyrin-Azobenzene-Bodipy Triads: Syntheses, Structures, and Photophysical Properties. Organic letters, 2017, 19, 2654-2657 |
| 1556050 | CIF | C27 H23 N O3 S | P 21 21 21 | 11.4379; 12.8956; 15.0848 90; 90; 90 | 2225 | Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic letters, 2017, 19, 3111-3114 |
| 1556051 | CIF | C33 H26 Cl N O4 S | P 21 21 21 | 8.9355; 14.869; 20.8047 90; 90; 90 | 2764.2 | Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic letters, 2017, 19, 3111-3114 |
| 1556052 | CIF | C204 H280 N24 O20 S12 | P 1 21/n 1 | 22.6919; 27.504; 32.801 90; 93.8825; 90 | 20425 | Cholewiak, Agnieszka; Tycz, Agnieszka; Jurczak, Janusz 8-Propyldithieno[3,2-b:2',3'-e]pyridine-3,5-diamine (DITIPIRAM) Derivatives as Neutral Receptors Tailored for Binding of Carboxylates. Organic letters, 2017, 19, 3001-3004 |
| 1556053 | CIF | C22 H22 Cl N O6 | C 1 2 1 | 21.5482; 6.1634; 16.9021 90; 111.981; 90 | 2081.59 | Drelich, Piotr; Moczulski, Marek; Albrecht, Łukasz d<sup>0</sup>a<sup>3</sup> Synthon Equivalents for the Stereocontrolled Synthesis of Functionalized 1,4-Amino Alcohol Precursors. Organic letters, 2017, 19, 3143-3146 |
| 1556054 | CIF | C19 H18 N2 O2 S | P 1 21/n 1 | 7.8427; 22.614; 18.528 90; 93.229; 90 | 3280.8 | Wang, Xingyong; Liu, Chulong; Zeng, Xiaobao; Wang, Xuesong; Wang, Xinyan; Hu, Yuefei Ruthenium-Catalyzed Synthesis of Fused Tricyclic 1H-2,3-Dihydropyrimido[1,2-a]quinolines in One Step. Organic letters, 2017, 19, 3378-3381 |
| 1556055 | CIF | C19 H19 Cl N6 O | C 1 2 1 | 20.4899; 9.7314; 10.0601 90; 101.493; 90 | 1965.72 | Li, Dan; Wang, Kezhou; Wang, Linqing; Wang, Yuan; Wang, Pengxin; Liu, Xin; Yang, Dongxu; Wang, Rui Magnesium Catalysis Mediated Tetrazoles in Desymmetrization Reaction of Aziridines. Organic letters, 2017, 19, 3211-3214 |
| 1556056 | CIF | C17.5 H14 N2 O1.5 | P 21 21 21 | 7.1969; 9.884; 38.6328 90; 90; 90 | 2748.11 | Mei, Guang-Jian; Bian, Chen-Yu; Li, Guo-Hao; Xu, Shao-Li; Zheng, Wen-Qin; Shi, Feng Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization. Organic letters, 2017, 19, 3219-3222 |
| 1556057 | CIF | C14 H10 N2 O2 | P b c a | 8.0739; 10.2485; 27.568 90; 90; 90 | 2281.1 | Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O. Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers. Organic letters, 2017, 19, 3512-3515 |
| 1556058 | CIF | C18 H18 N2 O3 | C 1 2/c 1 | 34.507; 7.3494; 13.4613 90; 110.662; 90 | 3194.3 | Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O. Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers. Organic letters, 2017, 19, 3512-3515 |
| 1556059 | CIF | C26 H22 N4 | P -1 | 4.8303; 9.8898; 22.174 99.193; 94.117; 98.243 | 1030 | Nallagangula, Madhu; Namitharan, Kayambu Copper-Catalyzed Sulfonyl Azide-Alkyne Cycloaddition Reactions: Simultaneous Generation and Trapping of Copper-Triazoles and -Ketenimines for the Synthesis of Triazolopyrimidines. Organic letters, 2017, 19, 3536-3539 |
| 1556060 | CIF | C20 H34 O10 Si | P 1 21 1 | 9.5791; 8.5119; 15.0831 90; 100.912; 90 | 1207.58 | Fegheh-Hassanpour, Younes; Arif, Tanzeel; Sintim, Herman O.; Al Mamari, Hamad H.; Hodgson, David M. Synthesis of (-)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition-Rearrangement and Cross-electrophile Coupling. Organic letters, 2017, 19, 3540-3543 |
| 1556061 | CIF | C21 H18 Br2 O5 | P 1 21 1 | 10.1616; 8.0804; 12.874 90; 98.272; 90 | 1046.1 | Zhong, Xingren; Lv, Jian; Luo, Sanzhong Enantio- and Diastereoselective Cyclopropanation of β,γ-Unsaturated α-Ketoester by a Chiral Phosphate/Indium(III) Complex. Organic letters, 2017, 19, 3331-3334 |
| 1556062 | CIF | C14 H22 O2 | P b c a | 9.3826; 13.5881; 18.663 90; 90; 90 | 2379.38 | Takatori, Kazuhiko; Ota, Shoya; Tendo, Kenta; Matsunaga, Kazuma; Nagasawa, Kokoro; Watanabe, Shinya; Kishida, Atsushi; Kogen, Hiroshi; Nagaoka, Hiroto Synthesis of Methylenebicyclo[3.2.1]octanol by a Sm(II)-Induced 1,2-Rearrangement Reaction with Ring Expansion of Methylenebicyclo[4.2.0]octanone. Organic letters, 2017, 19, 3763-3766 |
| 1556063 | CIF | C19 H38 O4 S Si | P 1 21 1 | 12.0435; 8.0033; 23.937 90; 102.088; 90 | 2256.1 | Santalla, Hugo; Faza, Olalla Nieto; Gómez, Generosa; Fall, Yagamare; Silva López, Carlos From Hydrindane to Decalin: A Mild Transformation through a Dyotropic Ring Expansion. Organic letters, 2017, 19, 3648-3651 |
| 1556064 | CIF | C16 H20 N2 O2 | P 1 21 1 | 8.6959; 9.773; 8.8762 90; 93.14; 90 | 753.2 | Wang, Jie; Wang, Lili; Guo, Shan; Zha, Shanke; Zhu, Jin Synthesis of 2,3-Benzodiazepines via Rh(III)-Catalyzed C-H Functionalization of N-Boc Hydrazones with Diazoketoesters. Organic letters, 2017, 19, 3640-3643 |
| 1556065 | CIF | C15 H18 O | C 1 2/c 1 | 34.436; 8.0667; 24.298 90; 134.486; 90 | 4815.3 | Su, Naijing; Deng, Tianning; Wink, Donald J.; Driver, Tom G. Achieving Site Selectivity in Metal-Catalyzed Electron-Rich Carbene Transfer Reactions from N-Tosylhydrazones. Organic letters, 2017, 19, 3990-3993 |
| 1556066 | CIF | C20 H21 N O4 S | P 1 21/n 1 | 6.949; 21.165; 12.887 90; 105.15; 90 | 1829.5 | Liu, Liu; Chen, Kun; Wu, Wen-Zhen; Wang, Peng-Fei; Song, Hang-Yu; Sun, Hongbin; Wen, Xiaoan; Xu, Qing-Long Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals. Organic letters, 2017, 19, 3823-3826 |
| 1556067 | CIF | C37 H37 Br O3 | P 1 21 1 | 9.4312; 11.6729; 14.7247 90; 100.851; 90 | 1592.1 | Liu, Shuai; Lan, Xin-Chan; Chen, Ke; Hao, Wen-Juan; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo Ag/Brønsted Acid Co-Catalyzed Spiroketalization of β-Alkynyl Ketones toward Spiro[chromane-2,1'-isochromene] Derivatives. Organic letters, 2017, 19, 3831-3834 |
| 1556068 | CIF | C36 H28 B N | P 1 21/c 1 | 8.7223; 12.0422; 24.8833 90; 92.4013; 90 | 2611.34 | Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents. Organic letters, 2017, 19, 3851-3854 |
| 1556069 | CIF | C46 H36 B N | P 1 21/n 1 | 13.779; 10.4066; 24.1478 90; 103.533; 90 | 3366.47 | Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents. Organic letters, 2017, 19, 3851-3854 |
| 1556070 | CIF | C46 H36 B N | P 1 21/c 1 | 11.74; 19.9773; 15.4637 90; 110.826; 90 | 3389.8 | Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents. Organic letters, 2017, 19, 3851-3854 |
| 1556071 | CIF | C30 H26 B N | P 1 21/c 1 | 10.4947; 12.3025; 17.1963 90; 95.954; 90 | 2208.3 | Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents. Organic letters, 2017, 19, 3851-3854 |
| 1556072 | CIF | C30 H26 B N | P 1 21/n 1 | 9.1115; 14.7945; 16.9449 90; 100.664; 90 | 2244.7 | Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents. Organic letters, 2017, 19, 3851-3854 |
| 1556073 | CIF | C28 H36 O8 | P 1 21 1 | 11.6927; 16.4378; 15.7568 90; 108.557; 90 | 2871.03 | Yin, Guo-Ping; Wu, Ya-Rong; Yang, Ming-Hua; Li, Tian-Xiao; Wang, Xiao-Bing; Zhou, Miao-Miao; Lei, Jian-Li; Kong, Ling-Yi Citrifurans A-D, Four Dimeric Aromatic Polyketides with New Carbon Skeletons from the Fungus Aspergillus sp. Organic letters, 2017, 19, 4058-4061 |
| 1556074 | CIF | C22 H26 N3 O3.5 S | P 21 21 21 | 12.3073; 18.643; 20.256 90; 90; 90 | 4647.6 | Hajra, Saumen; Singha Roy, Somnath; Aziz, Sk Mohammad; Das, Dhiraj Catalyst-Free "On-Water" Regio- and Stereospecific Ring-Opening of Spiroaziridine Oxindole: Enantiopure Synthesis of Unsymmetrical 3,3'-Bisindoles. Organic letters, 2017, 19, 4082-4085 |
| 1556075 | CIF | C20 H21 N O2 | P -1 | 8.8357; 10.6795; 10.7206 63.805; 75.002; 71.138 | 850.9 | Mandal, Anup; Sahoo, Harekrishna; Dana, Suman; Baidya, Mahiuddin Ruthenium(II)-Catalyzed Hydroarylation of Maleimides Using Carboxylic Acids as a Traceless Directing Group. Organic letters, 2017, 19, 4138-4141 |
| 1556076 | CIF | C17 H16 N2 O3 S | P 1 21/n 1 | 10.585; 9.1046; 16.2981 90; 93.8838; 90 | 1567.08 | Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides. Organic letters, 2017, 19, 6108-6111 |
| 1556077 | CIF | C15 H14 N2 O4 S | P 1 21/n 1 | 10.3618; 9.18131; 15.6457 90; 90.094; 90 | 1488.45 | Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides. Organic letters, 2017, 19, 6108-6111 |
| 1556078 | CIF | C14 H11 Br F N O | P n a 21 | 10.145; 26.485; 4.785 90; 90; 90 | 1285.7 | Gupta, Ekta; Kant, Ruchir; Mohanan, Kishor Decarbethoxylative Arylation Employing Arynes: A Metal-Free Pathway to Arylfluoroamides. Organic letters, 2017, 19, 6016-6019 |
| 1556099 | CIF | C49 H62 O7 | P -1 | 11.179; 13.411; 14.382 84.26; 83.38; 85.51 | 2126.2 | Stephan, ?; Gloe, ?; Paulus, ?; Saadioui, ?; Böhmer, V, ? Calix Crowns Derived from para-Bridged Calix Organic letters, 2000, 2, 839-841 |
| 1556100 | CIF | C13 H20 O2 S | P -1 | 10.016; 11.499; 17.53 95.938; 100.417; 108.57 | 1854 | Dawid, M.; Mlostoñ, G; Warkentin, J. The first 2,2-dialkoxythiirane. Organic letters, 2001, 3, 2455-2456 |
| 1556101 | CIF | C52 H48 N4 O3 | P -1 | 9.935; 15.483; 15.666 66.557; 76.89; 77.978 | 2134.4 | McCarthy, Jason R.; Jenkins, Hilary A.; Brückner, Christian Free base meso-tetraaryl-morpholinochlorins and porpholactone from meso-tetraaryl-2,3-dihydroxy-chlorin. Organic letters, 2003, 5, 19-22 |
| 1556102 | CIF | C19 H18 I N O4 | P 21 21 21 | 9.2879; 9.8237; 19.8438 90; 90; 90 | 1810.6 | Li, Guigen; Xu, Xin; Chen, Dianjun; Timmons, Cody; Carducci, Michael D.; Headley, Allan D. Asymmetric halo aldol reaction (AHA). Organic letters, 2003, 5, 329-331 |
| 1556103 | CIF | C68 H92 Se10 | P -1 | 10.459; 12.983; 13.711 101.621; 96.648; 94.94 | 1799.9 | Pietschnig, Rudolf; Schäfer, Sven; Merz, Klaus Self-addition of a sterically hindered alkynylselenolate. Organic letters, 2003, 5, 1867-1869 |
| 1556104 | CIF | C19 H19 N O3 S | P 1 21/c 1 | 11.0472; 7.6308; 19.6869 90; 92.423; 90 | 1658.1 | Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince New strategy for the synthesis of tetrahydroisoquinoline alkaloids. Organic letters, 2003, 5, 2181-2184 |
| 1556105 | CIF | C13 H14 N2 O3 | P 21 21 21 | 7.572; 10.031; 15.754 90; 90; 90 | 1196.59 | Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince New strategy for the synthesis of tetrahydroisoquinoline alkaloids. Organic letters, 2003, 5, 2181-2184 |
| 1556106 | CIF | C28 H16 F6 O2 | C c c 2 | 19.3494; 20.3274; 22.3761 90; 90; 90 | 8801 | Brizius, Glen; Billingsley, Kelvin; Smith, Mark D.; Bunz, Uwe H. F. Conformational and electronic engineering of twisted diphenylacetylenes. Organic letters, 2003, 5, 3951-3954 |
| 1556107 | CIF | C27 H40 O Si2 Sn | P 1 c 1 | 11.8381; 11.6026; 22.301 90; 104.522; 90 | 2965.2 | Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R. Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne. Organic letters, 2003, 5, 3971-3974 |
| 1556108 | CIF | C24.6 H32.8 Cl O1.3 Si2 | I 41/a :2 | 33.3269; 33.3269; 9.8038 90; 90; 90 | 10888.9 | Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R. Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne. Organic letters, 2003, 5, 3971-3974 |
| 1556109 | CIF | C67.5 H54.5 Br2 Cl2 N2 O6 P2 Ru | P 1 21 1 (c,2*a+c,b) | 16.649; 19.163; 27.224 90; 90; 89.58 | 8685.4 | Xu, Yingjian; Alcock, Nat W.; Clarkson, Guy J.; Docherty, Gordon; Woodward, Gary; Wills, Martin Asymmetric hydrogenation of ketones using a ruthenium(II) catalyst containing BINOL-derived monodonor phosphorus-donor ligands. Organic letters, 2004, 6, 4105-4107 |
| 1556110 | CIF | C23 H21 Br O10 | P 1 21 1 | 9.1105; 9.7461; 13.7386 90; 101.569; 90 | 1195.09 | Tanaka, Ken; Nishida, Goushi; Ogino, Masakazu; Hirano, Masao; Noguchi, Keiichi Enantioselective synthesis of axially chiral biaryls through rhodium-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes. Organic letters, 2005, 7, 3119-3121 |
| 1556111 | CIF | C21 H22 Cl N O5 | P 1 21 1 | 11.9029; 6.4499; 13.0137 90; 99.747; 90 | 984.67 | Weisser, Roland; Yue, Weimin; Reiser, Oliver Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure. Organic letters, 2005, 7, 5353-5356 |
| 1556112 | CIF | C20 H20 O5 | P 21 21 21 | 5.7104; 14.5249; 20.567 90; 90; 90 | 1705.9 | Weisser, Roland; Yue, Weimin; Reiser, Oliver Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure. Organic letters, 2005, 7, 5353-5356 |
| 1556113 | CIF | C7 H8 O5 | P 21 21 21 | 5.31; 10.8386; 12.8074 90; 90; 90 | 737.1 | Weisser, Roland; Yue, Weimin; Reiser, Oliver Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure. Organic letters, 2005, 7, 5353-5356 |
| 1556114 | CIF | C18 H20 Cl N O | P 1 | 9.0186; 10.1685; 10.338 106.26; 92.413; 114.734 | 812.73 | Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi Rhodium-catalyzed chemo-, regio-, and enantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates. Organic letters, 2005, 7, 4737-4739 |
| 1556115 | CIF | C22 H19 N O2 S | P 1 21 1 | 7.9578; 20.7251; 11.7791 90; 110.834; 90 | 1815.66 | Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi Rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide. Organic letters, 2006, 8, 907-909 |
| 1556116 | CIF | C24.5 H26 N O4.5 S | C 1 2 1 | 25.446; 5.8028; 16.3488 90; 110.637; 90 | 2259.1 | Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides. Organic letters, 2007, 9, 1307-1310 |
| 1556117 | CIF | C31 H27 N O4 S | P 21 21 21 | 10.2528; 10.7389; 47.533 90; 90; 90 | 5233.6 | Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides. Organic letters, 2007, 9, 1307-1310 |
| 1556118 | CIF | C27 H31 N O4 | C 1 2 1 | 15.411; 10.323; 30.625 90; 103.583; 90 | 4736 | Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R. Diels-Alder reactions of cyclic isoimidium salts. Organic letters, 2010, 12, 4524-4527 |
| 1556119 | CIF | C10 H16 O3 | P 1 21/n 1 | 5.2334; 15.5632; 11.7443 90; 91.016; 90 | 956.4 | Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R. Diels-Alder reactions of cyclic isoimidium salts. Organic letters, 2010, 12, 4524-4527 |
| 1556120 | CIF | C20 H19 N O3 | P 21 21 21 | 8.715; 9.891; 19.206 90; 90; 90 | 1655.6 | Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R. Diels-Alder reactions of cyclic isoimidium salts. Organic letters, 2010, 12, 4524-4527 |
| 1556121 | CIF | C27 H29 N O3 | P 21 21 21 | 9.4597; 10.0663; 23.0589 90; 90; 90 | 2195.8 | Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R. Diels-Alder reactions of cyclic isoimidium salts. Organic letters, 2010, 12, 4524-4527 |
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