Crystallography Open Database

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1556002 CIFC29 H28 N2 O3P 1 21/c 112.7136; 19.6481; 10.0368
90; 104.806; 90
2423.9Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556003 CIFC29 H28 N2 O3P 1 21/c 18.088; 29.039; 10.3957
90; 98.253; 90
2416.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556004 CIFC28 H26 N2 O3P -19.715; 11.622; 13.28
64.317; 86.248; 74.246
1298.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556005 CIFC26 H30 N2 O3P 1 21/c 111.5919; 14.5845; 13.8674
90; 97.872; 90
2322.4Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556006 CIFC34 H36 Cl2 N2 O5P 1 21/c 110.3241; 23.365; 13.7004
90; 99.642; 90
3258.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556007 CIFC33 H34 N2 O5P 1 21/c 113.9135; 11.8443; 18.4125
90; 108.518; 90
2877.2Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556008 CIFC29.5 H29 Cl N2 O3 SP 32 2 118.4813; 18.4813; 16.4257
90; 90; 120
4858.7Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556009 CIFC26 H30 N2 O3P 1 21/n 19.5688; 10.3956; 23.8948
90; 96.847; 90
2359.9Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556010 CIFC24 H24 N2 O2P 1 21/c 110.9969; 11.8906; 15.8497
90; 106.796; 90
1984.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556011 CIFC33 H34 N2 O5P 1 21/c 116.2583; 8.9359; 19.545
90; 95.231; 90
2827.7Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556012 CIFC26 H30 N2 O3P 1 21/c 115.2433; 10.1136; 14.943
90; 94.937; 90
2295.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556013 CIFC29 H28 N2 O3P 1 21/c 17.8226; 30.639; 10.1141
90; 98.682; 90
2396.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556014 CIFC29 H28 N2 O3 SP 1 21/c 18.6571; 29.45; 10.2183
90; 98.7924; 90
2574.56Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556015 CIFC26 H30 N2 O3C 1 2/c 117.3068; 12.0144; 22.5999
90; 96.044; 90
4673.1Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556016 CIFC29 H28 N2 O3C 1 2 122.49; 5.1816; 20.19
90; 90.78; 90
2352.6Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556017 CIFC29 H28 N2 O3 SP 1 21/n 119.7344; 12.7882; 20.279
90; 97.031; 90
5079.3Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg
Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters.
Organic letters, 2017, 19, 674-677
1556018 CIFC23 H17 Cl O3C 1 2 120.5553; 9.5675; 22.2196
90; 115.687; 90
3937.9Infante, Rebeca; Martin-Alvarez, Jose M; Andrés, Celia; Nieto, Javier
Dimethylzinc-Mediated Addition of Phenylacetylene to α-Diketones Catalyzed by Chiral Perhydro-1,3-benzoxazines.
Organic letters, 2017, 19, 1516-1519
1556019 CIFC16 H11 F N2 OP 21 21 218.4334; 9.1934; 16.9142
90; 90; 90
1311.4Jin, Yushu; Chen, Ming; Ge, Shaozhong; Hartwig, John F.
Palladium-Catalyzed, Enantioselective α-Arylation of α-Fluorooxindoles.
Organic letters, 2017, 19, 1390-1393
1556020 CIFC15 H12 N2 OP 1 21/n 116.4017; 7.1335; 20.0858
90; 95.665; 90
2338.6Yin, Kun; Zhang, Ronghua
Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature.
Organic letters, 2017, 19, 1530-1533
1556021 CIFC16 H14 N2 OP n a 219.9288; 26.7988; 4.7384
90; 90; 90
1260.79Yin, Kun; Zhang, Ronghua
Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature.
Organic letters, 2017, 19, 1530-1533
1556022 CIFC17 H13 N OP 1 21/c 14.0198; 13.908; 23.21
90; 94.2; 90
1294.1Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin
I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines.
Organic letters, 2017, 19, 1550-1553
1556023 CIFC11 H13 N S2P 1 21 19.9321; 22.705; 19.824
90; 98.538; 90
4420.9Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin
I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines.
Organic letters, 2017, 19, 1550-1553
1556024 CIFC43 H30 N2 O2P -110.4789; 12.074; 12.5011
92.552; 94.697; 98.319
1557.2Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling
Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions.
Organic letters, 2017, 19, 1658-1661
1556025 CIFC42 H28 N2 O2P b c a18.5446; 17.7946; 18.9442
90; 90; 90
6251.5Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling
Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions.
Organic letters, 2017, 19, 1658-1661
1556026 CIFC47 H36 Cl2 N4 O S ZnP -111.0032; 12.6313; 14.724
98.868; 96.16; 102.84
1950Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak
Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality.
Organic letters, 2017, 19, 1722-1725
1556027 CIFC51 H37 N5 O S ZnP 110.6689; 10.8762; 18.2817
83.457; 84.152; 77.519
2051.2Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak
Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality.
Organic letters, 2017, 19, 1722-1725
1556028 CIFC32 H27 Br O2P 1 21 19.624; 31.096; 13.229
90; 91.141; 90
3958Perveen, Saima; Zhao, Zhifei; Zhang, Guoxiang; Liu, Jian; Anwar, Muhammad; Fang, Xinqiang
Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis.
Organic letters, 2017, 19, 2470-2473
1556029 CIFC94 H64 O2P -19.9734; 11.3386; 15.3837
79.9686; 85.4756; 79.5603
1682.69Vadehra, Geeta S.; Jiang, Xing; Dotson, Jordan J.; Chu, Gong M.; Garcia-Garibay, Miguel A
High-Yielding and Divergent Paradigm for the Synthesis of D<sub>2h</sub>-Symmetric Octakis-Substituted Pentiptycenequinones.
Organic letters, 2017, 19, 1838-1841
1556030 CIFC24 H26 N2 O6P 1 21 111.0167; 8.4713; 13.145
90; 112.969; 90
1129.5Ran, Guang-Yao; Gong, Ming; Yue, Jing-Fei; Yang, Xing-Xing; Zhou, Su-Lan; Du, Wei; Chen, Ying-Chun
Asymmetric Cascade Assembly of 1,2-Diaza-1,3-dienes and α,β-Unsaturated Aldehydes via Dienamine Activation.
Organic letters, 2017, 19, 1874-1877
1556031 CIFC14 H9 N O3 SP 1 21/c 112.0277; 13.0209; 8.1447
90; 106.121; 90
1225.4Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556032 CIFC14 H13 N O3 SP 21 21 217.4865; 10.7242; 32.3467
90; 90; 90
2597.01Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556033 CIFC14 H12 N O3 SP 21 21 219.4952; 13.78766; 23.3234
90; 90; 90
3053.42Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara
Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation.
Organic letters, 2017, 19, 2042-2045
1556034 CIFC24 H24 N2 O3 SeP 1 21/c 19.4838; 10.5004; 21.1264
90; 90.868; 90
2103.6Foley, Christopher; Shaw, Arthur; Hulme, Christopher
Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles.
Organic letters, 2017, 19, 2238-2241
1556035 CIFC14 H16 N4 OP 1 21/m 17.7378; 6.7075; 12.6395
90; 102.323; 90
640.89Foley, Christopher; Shaw, Arthur; Hulme, Christopher
Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles.
Organic letters, 2017, 19, 2238-2241
1556036 CIFC28 H44 Cl2 N8 Ni O2I m -3 m17.0714; 17.0714; 17.0714
90; 90; 90
4975.2Zhang, Xingjie; Xia, Aiyou; Chen, Haoyi; Liu, Yuanhong
General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)<sub>2</sub>: Key Roles of DMAP.
Organic letters, 2017, 19, 2118-2121
1556037 CIFC23 H18 O2P 1 21 16.0965; 7.8294; 17.9271
90; 96.951; 90
849.41Zhang, Jingfang; Tang, Yuhai; Wei, Wen; Wu, Yong; Li, Yang; Zhang, Junjie; Zheng, Yuansuo; Xu, Silong
Organocatalytic Cloke-Wilson Rearrangement: DABCO-Catalyzed Ring Expansion of Cyclopropyl Ketones to 2,3-Dihydrofurans.
Organic letters, 2017, 19, 3043-3046
1556038 CIFC26 H34 O4 SiP 21 21 219.47; 15.075; 17.824
90; 90; 90
2544.6Han, Man-Yi; Xie, Xiaoyu; Zhou, Di; Li, Pinhua; Wang, Lei
Organocatalyzed Direct Aldol Reaction of Silyl Glyoxylates for the Synthesis of α-Hydroxysilanes.
Organic letters, 2017, 19, 2282-2285
1556039 CIFC16 H13 Br F3 N O3P 21 21 215.8132; 8.851; 31.166
90; 90; 90
1603.6Wang, Pei; Li, Hong-Feng; Zhao, Jia-Zhen; Du, Zhi-Hong; Da, Chao-Shan
Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones.
Organic letters, 2017, 19, 2634-2637
1556040 CIFC22 H26 O4 SP b c a5.5413; 15.8031; 45.3572
90; 90; 90
3971.92Zhurakovskyi, Oleksandr; Ellis, Sam R.; Thompson, Amber L.; Robertson, Jeremy
Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland-Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl.
Organic letters, 2017, 19, 2174-2177
1556041 CIFC19 H37 Br Cu N3 P2I 41 c d31.5316; 31.5316; 18.8701
90; 90; 90
18761.4Mastalir, Matthias; Pittenauer, Ernst; Stöger, Berthold; Allmaier, Günter; Kirchner, Karl
Three Different Reactions, One Catalyst: A Cu(I) PNP Pincer Complex as Catalyst for C-C and C-N Cross-Couplings.
Organic letters, 2017, 19, 2178-2181
1556042 CIFC27 H22 O SP 21 21 215.3756; 8.23448; 44.3104
90; 90; 90
1961.41Wang, Zhaobin; Sun, Jianwei
Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes.
Organic letters, 2017, 19, 2334-2337
1556043 CIFC11 H10 F7 N3 O2P 1 21/c 116.1302; 7.5328; 12.1195
90; 90.161; 90
1472.6Wang, Rui; Guan, Wei; Han, Zheng-Bo; Liang, Fushun; Suga, Takeo; Bi, Xihe; Nishide, Hiroyuki
Ambient-Light-Promoted Three-Component Annulation: Synthesis of Perfluoroalkylated Pyrimidines.
Organic letters, 2017, 19, 2358-2361
1556044 CIFC25 H31 N O7 SiP -19.5604; 11.3393; 12.5938
64.094; 79.058; 86.136
1205.56Parsons, Philip J.; Jones, Daniel R.; Walsh, Lee J.; Allen, Lewis A. T.; Onwubiko, Ada; Preece, Lewis; Board, Johnathan; White, Andrew J. P.
An Approach to the Core of Lactonamycin.
Organic letters, 2017, 19, 2533-2535
1556045 CIFC19 H20 O3C 1 2 117.9303; 6.8625; 13.4226
90; 99.456; 90
1629.16Iwamoto, Hiroaki; Akiyama, Sota; Hayama, Keiichi; Ito, Hajime
Copper(I)-Catalyzed Stereo- and Chemoselective Borylative Radical Cyclization of Alkyl Halides Bearing an Alkene Moiety.
Organic letters, 2017, 19, 2614-2617
1556046 CIFC12 H6 O S2P b c a5.541; 15.387; 22.574
90; 90; 90
1925Mitsudo, Koichi; Kurimoto, Yuji; Mandai, Hiroki; Suga, Seiji
Synthesis of 3-Benzo[b]thienyl 3-Thienyl Ether via an Addition-Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its π-Extended Derivatives.
Organic letters, 2017, 19, 2821-2824
1556047 CIFC19 H26 Cl N2 O RhP b c a8.0471; 16.3426; 29.6614
90; 90; 90
3900.8Long, Zhen; Yang, Yudong; You, Jingsong
Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles.
Organic letters, 2017, 19, 2781-2784
1556048 CIFC22 H24 Cl N2 O RhP 1 21/n 17.58618; 16.9757; 15.6843
90; 93.0656; 90
2016.94Long, Zhen; Yang, Yudong; You, Jingsong
Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles.
Organic letters, 2017, 19, 2781-2784
1556049 CIFC116 H112 Cl2 N10 NiP -112.6554; 19.7134; 21.0374
72.334; 80.809; 82.734
4919.7Yin, Bangshao; Kim, Taeyeon; Zhou, Mingbo; Huang, Weiming; Kim, Dongho; Song, Jianxin
Porphyrin-Azobenzene-Bodipy Triads: Syntheses, Structures, and Photophysical Properties.
Organic letters, 2017, 19, 2654-2657
1556050 CIFC27 H23 N O3 SP 21 21 2111.4379; 12.8956; 15.0848
90; 90; 90
2225Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin
Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations.
Organic letters, 2017, 19, 3111-3114
1556051 CIFC33 H26 Cl N O4 SP 21 21 218.9355; 14.869; 20.8047
90; 90; 90
2764.2Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin
Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations.
Organic letters, 2017, 19, 3111-3114
1556052 CIFC204 H280 N24 O20 S12P 1 21/n 122.6919; 27.504; 32.801
90; 93.8825; 90
20425Cholewiak, Agnieszka; Tycz, Agnieszka; Jurczak, Janusz
8-Propyldithieno[3,2-b:2',3'-e]pyridine-3,5-diamine (DITIPIRAM) Derivatives as Neutral Receptors Tailored for Binding of Carboxylates.
Organic letters, 2017, 19, 3001-3004
1556053 CIFC22 H22 Cl N O6C 1 2 121.5482; 6.1634; 16.9021
90; 111.981; 90
2081.59Drelich, Piotr; Moczulski, Marek; Albrecht, Ɓukasz
d<sup>0</sup>a<sup>3</sup> Synthon Equivalents for the Stereocontrolled Synthesis of Functionalized 1,4-Amino Alcohol Precursors.
Organic letters, 2017, 19, 3143-3146
1556054 CIFC19 H18 N2 O2 SP 1 21/n 17.8427; 22.614; 18.528
90; 93.229; 90
3280.8Wang, Xingyong; Liu, Chulong; Zeng, Xiaobao; Wang, Xuesong; Wang, Xinyan; Hu, Yuefei
Ruthenium-Catalyzed Synthesis of Fused Tricyclic 1H-2,3-Dihydropyrimido[1,2-a]quinolines in One Step.
Organic letters, 2017, 19, 3378-3381
1556055 CIFC19 H19 Cl N6 OC 1 2 120.4899; 9.7314; 10.0601
90; 101.493; 90
1965.72Li, Dan; Wang, Kezhou; Wang, Linqing; Wang, Yuan; Wang, Pengxin; Liu, Xin; Yang, Dongxu; Wang, Rui
Magnesium Catalysis Mediated Tetrazoles in Desymmetrization Reaction of Aziridines.
Organic letters, 2017, 19, 3211-3214
1556056 CIFC17.5 H14 N2 O1.5P 21 21 217.1969; 9.884; 38.6328
90; 90; 90
2748.11Mei, Guang-Jian; Bian, Chen-Yu; Li, Guo-Hao; Xu, Shao-Li; Zheng, Wen-Qin; Shi, Feng
Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization.
Organic letters, 2017, 19, 3219-3222
1556057 CIFC14 H10 N2 O2P b c a8.0739; 10.2485; 27.568
90; 90; 90
2281.1Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O.
Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers.
Organic letters, 2017, 19, 3512-3515
1556058 CIFC18 H18 N2 O3C 1 2/c 134.507; 7.3494; 13.4613
90; 110.662; 90
3194.3Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O.
Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers.
Organic letters, 2017, 19, 3512-3515
1556059 CIFC26 H22 N4P -14.8303; 9.8898; 22.174
99.193; 94.117; 98.243
1030Nallagangula, Madhu; Namitharan, Kayambu
Copper-Catalyzed Sulfonyl Azide-Alkyne Cycloaddition Reactions: Simultaneous Generation and Trapping of Copper-Triazoles and -Ketenimines for the Synthesis of Triazolopyrimidines.
Organic letters, 2017, 19, 3536-3539
1556060 CIFC20 H34 O10 SiP 1 21 19.5791; 8.5119; 15.0831
90; 100.912; 90
1207.58Fegheh-Hassanpour, Younes; Arif, Tanzeel; Sintim, Herman O.; Al Mamari, Hamad H.; Hodgson, David M.
Synthesis of (-)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition-Rearrangement and Cross-electrophile Coupling.
Organic letters, 2017, 19, 3540-3543
1556061 CIFC21 H18 Br2 O5P 1 21 110.1616; 8.0804; 12.874
90; 98.272; 90
1046.1Zhong, Xingren; Lv, Jian; Luo, Sanzhong
Enantio- and Diastereoselective Cyclopropanation of β,γ-Unsaturated α-Ketoester by a Chiral Phosphate/Indium(III) Complex.
Organic letters, 2017, 19, 3331-3334
1556062 CIFC14 H22 O2P b c a9.3826; 13.5881; 18.663
90; 90; 90
2379.38Takatori, Kazuhiko; Ota, Shoya; Tendo, Kenta; Matsunaga, Kazuma; Nagasawa, Kokoro; Watanabe, Shinya; Kishida, Atsushi; Kogen, Hiroshi; Nagaoka, Hiroto
Synthesis of Methylenebicyclo[3.2.1]octanol by a Sm(II)-Induced 1,2-Rearrangement Reaction with Ring Expansion of Methylenebicyclo[4.2.0]octanone.
Organic letters, 2017, 19, 3763-3766
1556063 CIFC19 H38 O4 S SiP 1 21 112.0435; 8.0033; 23.937
90; 102.088; 90
2256.1Santalla, Hugo; Faza, Olalla Nieto; Gómez, Generosa; Fall, Yagamare; Silva López, Carlos
From Hydrindane to Decalin: A Mild Transformation through a Dyotropic Ring Expansion.
Organic letters, 2017, 19, 3648-3651
1556064 CIFC16 H20 N2 O2P 1 21 18.6959; 9.773; 8.8762
90; 93.14; 90
753.2Wang, Jie; Wang, Lili; Guo, Shan; Zha, Shanke; Zhu, Jin
Synthesis of 2,3-Benzodiazepines via Rh(III)-Catalyzed C-H Functionalization of N-Boc Hydrazones with Diazoketoesters.
Organic letters, 2017, 19, 3640-3643
1556065 CIFC15 H18 OC 1 2/c 134.436; 8.0667; 24.298
90; 134.486; 90
4815.3Su, Naijing; Deng, Tianning; Wink, Donald J.; Driver, Tom G.
Achieving Site Selectivity in Metal-Catalyzed Electron-Rich Carbene Transfer Reactions from N-Tosylhydrazones.
Organic letters, 2017, 19, 3990-3993
1556066 CIFC20 H21 N O4 SP 1 21/n 16.949; 21.165; 12.887
90; 105.15; 90
1829.5Liu, Liu; Chen, Kun; Wu, Wen-Zhen; Wang, Peng-Fei; Song, Hang-Yu; Sun, Hongbin; Wen, Xiaoan; Xu, Qing-Long
Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals.
Organic letters, 2017, 19, 3823-3826
1556067 CIFC37 H37 Br O3P 1 21 19.4312; 11.6729; 14.7247
90; 100.851; 90
1592.1Liu, Shuai; Lan, Xin-Chan; Chen, Ke; Hao, Wen-Juan; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Ag/Brønsted Acid Co-Catalyzed Spiroketalization of β-Alkynyl Ketones toward Spiro[chromane-2,1'-isochromene] Derivatives.
Organic letters, 2017, 19, 3831-3834
1556068 CIFC36 H28 B NP 1 21/c 18.7223; 12.0422; 24.8833
90; 92.4013; 90
2611.34Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556069 CIFC46 H36 B NP 1 21/n 113.779; 10.4066; 24.1478
90; 103.533; 90
3366.47Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556070 CIFC46 H36 B NP 1 21/c 111.74; 19.9773; 15.4637
90; 110.826; 90
3389.8Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556071 CIFC30 H26 B NP 1 21/c 110.4947; 12.3025; 17.1963
90; 95.954; 90
2208.3Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556072 CIFC30 H26 B NP 1 21/n 19.1115; 14.7945; 16.9449
90; 100.664; 90
2244.7Mellerup, Soren K.; Häfele, Lisa; Lorbach, Andreas; Wang, Xiang; Wang, Suning
Triplet Energy and π-Conjugation Effects on Photoisomerization of Chiral N,C-Chelate Organoborons with PAH Substituents.
Organic letters, 2017, 19, 3851-3854
1556073 CIFC28 H36 O8P 1 21 111.6927; 16.4378; 15.7568
90; 108.557; 90
2871.03Yin, Guo-Ping; Wu, Ya-Rong; Yang, Ming-Hua; Li, Tian-Xiao; Wang, Xiao-Bing; Zhou, Miao-Miao; Lei, Jian-Li; Kong, Ling-Yi
Citrifurans A-D, Four Dimeric Aromatic Polyketides with New Carbon Skeletons from the Fungus Aspergillus sp.
Organic letters, 2017, 19, 4058-4061
1556074 CIFC16 H18.18 N2.18 O2.55 S0.73P 21 21 2112.3073; 18.643; 20.256
90; 90; 90
4647.6Hajra, Saumen; Singha Roy, Somnath; Aziz, Sk Mohammad; Das, Dhiraj
Catalyst-Free "On-Water" Regio- and Stereospecific Ring-Opening of Spiroaziridine Oxindole: Enantiopure Synthesis of Unsymmetrical 3,3'-Bisindoles.
Organic letters, 2017, 19, 4082-4085
1556075 CIFC20 H21 N O2P -18.8357; 10.6795; 10.7206
63.805; 75.002; 71.138
850.9Mandal, Anup; Sahoo, Harekrishna; Dana, Suman; Baidya, Mahiuddin
Ruthenium(II)-Catalyzed Hydroarylation of Maleimides Using Carboxylic Acids as a Traceless Directing Group.
Organic letters, 2017, 19, 4138-4141
1556076 CIFC17 H16 N2 O3 SP 1 21/n 110.585; 9.1046; 16.2981
90; 93.8838; 90
1567.08Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang
Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides.
Organic letters, 2017, 19, 6108-6111
1556077 CIFC15 H14 N2 O4 SP 1 21/n 110.3618; 9.18131; 15.6457
90; 90.094; 90
1488.45Han, Xiang-Lei; Zhou, Chu-Jun; Liu, Xu-Ge; Zhang, Shang-Shi; Wang, Honggen; Li, Qingjiang
Regioselective Synthesis of 5-Aminooxazoles via Cp*Co(III)-Catalyzed Formal [3 + 2] Cycloaddition of N-(Pivaloyloxy)amides with Ynamides.
Organic letters, 2017, 19, 6108-6111
1556078 CIFC14 H11 Br F N OP n a 2110.145; 26.485; 4.785
90; 90; 90
1285.7Gupta, Ekta; Kant, Ruchir; Mohanan, Kishor
Decarbethoxylative Arylation Employing Arynes: A Metal-Free Pathway to Arylfluoroamides.
Organic letters, 2017, 19, 6016-6019
1556099 CIFC49 H62 O7P -111.179; 13.411; 14.382
84.26; 83.38; 85.51
2126.2Stephan, ?; Gloe, ?; Paulus, ?; Saadioui, ?; Böhmer, V, ?
Calix Crowns Derived from para-Bridged Calix
Organic letters, 2000, 2, 839-841
1556100 CIFC13 H20 O2 SP -110.016; 11.499; 17.53
95.938; 100.417; 108.57
1854Dawid, M.; Mlostoñ, G; Warkentin, J.
The first 2,2-dialkoxythiirane.
Organic letters, 2001, 3, 2455-2456
1556101 CIFC52 H48 N4 O3P -19.935; 15.483; 15.666
66.557; 76.89; 77.978
2134.4McCarthy, Jason R.; Jenkins, Hilary A.; Brückner, Christian
Free base meso-tetraaryl-morpholinochlorins and porpholactone from meso-tetraaryl-2,3-dihydroxy-chlorin.
Organic letters, 2003, 5, 19-22
1556102 CIFC19 H18 I N O4P 21 21 219.2879; 9.8237; 19.8438
90; 90; 90
1810.6Li, Guigen; Xu, Xin; Chen, Dianjun; Timmons, Cody; Carducci, Michael D.; Headley, Allan D.
Asymmetric halo aldol reaction (AHA).
Organic letters, 2003, 5, 329-331
1556103 CIFC68 H92 Se10P -110.459; 12.983; 13.711
101.621; 96.648; 94.94
1799.9Pietschnig, Rudolf; Schäfer, Sven; Merz, Klaus
Self-addition of a sterically hindered alkynylselenolate.
Organic letters, 2003, 5, 1867-1869
1556104 CIFC19 H19 N O3 SP 1 21/c 111.0472; 7.6308; 19.6869
90; 92.423; 90
1658.1Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556105 CIFC13 H14 N2 O3P 21 21 217.572; 10.031; 15.754
90; 90; 90
1196.59Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556106 CIFC28 H16 F6 O2C c c 219.3494; 20.3274; 22.3761
90; 90; 90
8801Brizius, Glen; Billingsley, Kelvin; Smith, Mark D.; Bunz, Uwe H. F.
Conformational and electronic engineering of twisted diphenylacetylenes.
Organic letters, 2003, 5, 3951-3954
1556107 CIFC27 H40 O Si2 SnP 1 c 111.8381; 11.6026; 22.301
90; 104.522; 90
2965.2Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556108 CIFC24.6 H32.8 Cl O1.3 Si2I 41/a :233.3269; 33.3269; 9.8038
90; 90; 90
10888.9Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556109 CIFC67.5 H54.5 Br2 Cl2 N2 O6 P2 RuP 1 21 1 (c,2*a+c,b)16.649; 19.163; 27.224
90; 90; 89.58
8685.4Xu, Yingjian; Alcock, Nat W.; Clarkson, Guy J.; Docherty, Gordon; Woodward, Gary; Wills, Martin
Asymmetric hydrogenation of ketones using a ruthenium(II) catalyst containing BINOL-derived monodonor phosphorus-donor ligands.
Organic letters, 2004, 6, 4105-4107
1556110 CIFC23 H21 Br O10P 1 21 19.1105; 9.7461; 13.7386
90; 101.569; 90
1195.09Tanaka, Ken; Nishida, Goushi; Ogino, Masakazu; Hirano, Masao; Noguchi, Keiichi
Enantioselective synthesis of axially chiral biaryls through rhodium-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes.
Organic letters, 2005, 7, 3119-3121
1556111 CIFC21 H22 Cl N O5P 1 21 111.9029; 6.4499; 13.0137
90; 99.747; 90
984.67Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556112 CIFC20 H20 O5P 21 21 215.7104; 14.5249; 20.567
90; 90; 90
1705.9Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556113 CIFC7 H8 O5P 21 21 215.31; 10.8386; 12.8074
90; 90; 90
737.1Weisser, Roland; Yue, Weimin; Reiser, Oliver
Enantioselective synthesis of furo[2,3-b]furans, a spongiane diterpenoid substructure.
Organic letters, 2005, 7, 5353-5356
1556114 CIFC18 H20 Cl N OP 19.0186; 10.1685; 10.338
106.26; 92.413; 114.734
812.73Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi
Rhodium-catalyzed chemo-, regio-, and enantioselective [2 + 2 + 2] cycloaddition of alkynes with isocyanates.
Organic letters, 2005, 7, 4737-4739
1556115 CIFC22 H19 N O2 SP 1 21 17.9578; 20.7251; 11.7791
90; 110.834; 90
1815.66Tanaka, Ken; Wada, Azusa; Noguchi, Keiichi
Rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide.
Organic letters, 2006, 8, 907-909
1556116 CIFC24.5 H26 N O4.5 SC 1 2 125.446; 5.8028; 16.3488
90; 110.637; 90
2259.1Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao
Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides.
Organic letters, 2007, 9, 1307-1310
1556117 CIFC31 H27 N O4 SP 21 21 2110.2528; 10.7389; 47.533
90; 90; 90
5233.6Tanaka, Ken; Osaka, Takuya; Noguchi, Keiichi; Hirano, Masao
Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides.
Organic letters, 2007, 9, 1307-1310
1556118 CIFC27 H31 N O4C 1 2 115.411; 10.323; 30.625
90; 103.583; 90
4736Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556119 CIFC10 H16 O3P 1 21/n 15.2334; 15.5632; 11.7443
90; 91.016; 90
956.4Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556120 CIFC20 H19 N O3P 21 21 218.715; 9.891; 19.206
90; 90; 90
1655.6Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556121 CIFC27 H29 N O3P 21 21 219.4597; 10.0663; 23.0589
90; 90; 90
2195.8Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556122 CIFC26 H31 N O3P 21 21 218.5828; 13.808; 19.023
90; 90; 90
2254.4Boeckman, Jr, Robert K; Miller, Yan; Ryder, Todd R.
Diels-Alder reactions of cyclic isoimidium salts.
Organic letters, 2010, 12, 4524-4527
1556123 CIFC17 H28 Cl N Ni O SiP 1 21/n 111.287; 10.884; 15.828
90; 107.092; 90
1858.6Shrestha, Ruja; Weix, Daniel J.
Reductive conjugate addition of haloalkanes to enones to form silyl enol ethers.
Organic letters, 2011, 13, 2766-2769
1556124 CIFC26 H30 I N O5P 21 21 217.7887; 14.737; 21.142
90; 90; 90
2426.7Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J.
A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.
Organic letters, 2012, 14, 4082-4085
1556125 CIFC16 H19 N O5P 1 21 16.9621; 36.328; 6.9667
90; 117.642; 90
1560.9Ciesielski, Jennifer; Cariou, Kevin; Frontier, Alison J.
A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.
Organic letters, 2012, 14, 4082-4085
1556126 CIFC26 H28 N2 O4 SP 21 21 219.6487; 12.0714; 19.866
90; 90; 90
2313.9Sequeira, Fatima C.; Chemler, Sherry R.
Stereoselective synthesis of morpholines via copper-promoted oxyamination of alkenes.
Organic letters, 2012, 14, 4482-4485
1556127 CIFC12 H12 O7P -17.8732; 7.9554; 9.7428
91.356; 108.391; 92.72
577.93Meck, Christine; Mohd, Noushad; Murelli, Ryan P.
An oxidopyrylium cyclization/ring-opening route to polysubstituted α-hydroxytropolones.
Organic letters, 2012, 14, 5988-5991
1556128 CIFC15 H20 N4 O4P 21 21 2110.49; 10.995; 13.995
90; 90; 90
1614.1Ottersbach, Philipp A.; Schmitz, Janina; Schnakenburg, Gregor; Gütschow, Michael
An access to aza-Freidinger lactams and E-locked analogs.
Organic letters, 2013, 15, 448-451
1556129 CIFC15 H23 N O3P 1 21 111.479; 16.064; 12.35
90; 101.98; 90
2227.7Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556130 CIFC13 H19 N O3P 21 21 219.917; 10.626; 11.336
90; 90; 90
1194.6Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556131 CIFC13 H19 N O3P 21 21 218.431; 11.03; 13.069
90; 90; 90
1215.3Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556132 CIFC12 H17 N O6P 21 21 218.2; 10.542; 14.773
90; 90; 90
1277Lumbroso, Alexandre; Beaudet, Isabelle; Toupet, Loïc; Le Grognec, Erwan; Quintard, Jean-Paul
Stereodivergent synthesis of iminosugars from stannylated derivatives of (S)-vinylglycinol.
Organic letters, 2013, 15, 160-163
1556133 CIFC42 H46 N2 O2P -18.2943; 8.331; 13.551
101.869; 94.696; 114.24
820.9Balandier, Jean-Yves; Henry, Nicolas; Arlin, Jean-Baptiste; Sanguinet, Lionel; Lemaur, Vincent; Niebel, Claude; Chattopadhyay, Basab; Kennedy, Alan Robert; Leriche, Philippe; Blanchard, Philippe; Cornil, Jérôme; Geerts, Yves Henri
Synthesis and characterization of isomerically pure anti- and syn-anthradiindole derivatives.
Organic letters, 2013, 15, 302-305
1556134 CIFC43.82 H49.83 Cl3.45 N2 O2.67P 1 21/c 115.8497; 10.3321; 24.9736
90; 95.678; 90
4069.6Balandier, Jean-Yves; Henry, Nicolas; Arlin, Jean-Baptiste; Sanguinet, Lionel; Lemaur, Vincent; Niebel, Claude; Chattopadhyay, Basab; Kennedy, Alan Robert; Leriche, Philippe; Blanchard, Philippe; Cornil, Jérôme; Geerts, Yves Henri
Synthesis and characterization of isomerically pure anti- and syn-anthradiindole derivatives.
Organic letters, 2013, 15, 302-305
1556135 CIFC45 H28 Au2 Cl4 O4 P2P 1 21/c 110.834; 20.925; 17.732
90; 93.784; 90
4011.1Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556136 CIFC22 H13 O2 P SP -113.099; 13.122; 13.604
117.831; 117.735; 91.969
1733.1Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556137 CIFC22 H13 O3 PP b c a7.544; 17.023; 26.006
90; 90; 90
3339.7Chen, Hui; Delaunay, Wylliam; Li, Jing; Wang, Zuoyong; Bouit, Pierre-Antoine; Tondelier, Denis; Geffroy, Bernard; Mathey, François; Duan, Zheng; Réau, Régis; Hissler, Muriel
Benzofuran-fused phosphole: synthesis, electronic, and electroluminescence properties.
Organic letters, 2013, 15, 330-333
1556138 CIFC17 H20 O5P -18.39; 9.844; 10.32
76.55; 79.16; 89.73
813.5Barluenga, José; Álvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Ángel L; Tomás, Miguel
A simple metal-promoted three-step access to n/5/m angular carbocyclic systems.
Organic letters, 2013, 15, 488-491
1556139 CIFC17 H20 O5P -18.7914; 9.2136; 10.4275
95.867; 107.824; 103.956
766.06Barluenga, José; Álvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Ángel L; Tomás, Miguel
A simple metal-promoted three-step access to n/5/m angular carbocyclic systems.
Organic letters, 2013, 15, 488-491
1556140 CIFC22 H21 Cl O4P 15.7264; 7.5889; 21.5174
91.997; 94.434; 90.306
931.69Bastida, David; Liu, Yankai; Tian, Xu; Escudero-Adán, Eduardo; Melchiorre, Paolo
Asymmetric vinylogous aldol reaction via H-bond-directing dienamine catalysis.
Organic letters, 2013, 15, 220-223
1556141 CIFC30 H25 Cl O4P 21 21 218.3789; 11.6032; 23.8284
90; 90; 90
2316.65Bastida, David; Liu, Yankai; Tian, Xu; Escudero-Adán, Eduardo; Melchiorre, Paolo
Asymmetric vinylogous aldol reaction via H-bond-directing dienamine catalysis.
Organic letters, 2013, 15, 220-223
1556142 CIFC12 H18 N2 O3 SP 21 21 215.1292; 8.5021; 28.173
90; 90; 90
1228.6Schüttler, Christian; Li-Böhmer, Zhen; Harms, Klaus; von Zezschwitz, Paultheo
Enantioselective synthesis of 3,4-disubstituted cis- and trans-1,2,5-thiadiazolidine-1,1-dioxides as precursors for chiral 1,2-diamines.
Organic letters, 2013, 15, 800-803
1556143 CIFC41 H37 Cl3 I2 N2 O9 S4P -19.3373; 15.5995; 15.8053
84.143; 86.017; 84.742
2276.3Röben, Caren; Souto, José A; Escudero-Adán, Eduardo C; Muñiz, Kilian
Oxidative diamination promoted by dinuclear iodine(III) reagents.
Organic letters, 2013, 15, 1008-1011
1556144 CIFC21 H20 F5 N O2P 21 21 217.5446; 14.193; 17.9736
90; 90; 90
1924.62Fustero, Santos; Ibáñez, Ignacio; Barrio, Pablo; Maestro, Miguel A.; Catalán, Silvia
Gold-catalyzed intramolecular hydroamination of o-alkynylbenzyl carbamates: a route to chiral fluorinated isoindoline and isoquinoline derivatives.
Organic letters, 2013, 15, 832-835
1556145 CIFC50.5 H43 Cl I N O2P 21 21 2112.6747; 15.3867; 23.8253
90; 90; 90
4646.5Liu, Yan; Shirakawa, Seiji; Maruoka, Keiji
Phase-transfer-catalyzed asymmetric conjugate cyanation of alkylidenemalonates with KCN in the presence of a Brønsted acid additive.
Organic letters, 2013, 15, 1230-1233
1556146 CIFC17 H26 N4 O3C c c 214.754; 22.06; 5.146
90; 90; 90
1674.9Rigol, Stephan; Beyer, Lothar; Hennig, Lothar; Sieler, Joachim; Giannis, Athanassios
Hünlich base: (re)discovery, synthesis, and structure elucidation after a century.
Organic letters, 2013, 15, 1418-1420
1556147 CIFC29 H28 B Fe O PP 21 21 218.9007; 14.791; 17.7255
90; 90; 90
2333.57Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556148 CIFC29 H28 B Fe O PP 21 21 219.01; 14.7132; 17.6287
90; 90; 90
2336.97Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556149 CIFC27 H32 B Fe O PP 21 21 218.9778; 9.0335; 29.5925
90; 90; 90
2399.98Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556150 CIFC27 H32 B Fe O PP 21 21 219.1406; 9.7796; 27.2445
90; 90; 90
2435.42Rémond, Emmanuelle; Bayardon, Jérôme; Takizawa, Shinobu; Rousselin, Yoann; Sasai, Hiroaki; Jugé, Sylvain
o-(Hydroxyalkyl)phenyl P-chirogenic phosphines as functional chiral Lewis bases.
Organic letters, 2013, 15, 1870-1873
1556151 CIFC16 H13 N OP 1 21/c 111.237; 14.637; 7.2453
90; 99.56; 90
1175.1Liu, Le; Lu, Hang; Wang, Hong; Yang, Chao; Zhang, Xiang; Zhang-Negrerie, Daisy; Du, Yunfei; Zhao, Kang
PhI(OCOCF3)2-mediated C-C bond formation concomitant with a 1,2-aryl shift in a metal-free synthesis of 3-arylquinolin-2-ones.
Organic letters, 2013, 15, 2906-2909
1556152 CIFC56 H48 F8 N4P -18.695; 9.355; 13.874
104.83; 90.259; 90.583
1090.9Takase, Masayoshi; Inabe, Ayumi; Sugawara, Yuki; Fujita, Wataru; Nishinaga, Tohru; Nomura, Kotohiro
Donor-acceptor segregated paracyclophanes composed of naphthobipyrrole and stacked fluoroarenes.
Organic letters, 2013, 15, 3202-3205
1556153 CIFC40 H20 F8 N4C 1 2/c 120.8969; 25.977; 14.1722
90; 129.736; 90
5916.1Takase, Masayoshi; Inabe, Ayumi; Sugawara, Yuki; Fujita, Wataru; Nishinaga, Tohru; Nomura, Kotohiro
Donor-acceptor segregated paracyclophanes composed of naphthobipyrrole and stacked fluoroarenes.
Organic letters, 2013, 15, 3202-3205
1556154 CIFC18 H14 O3P 1 21/n 15.5563; 23.1971; 10.5069
90; 96.804; 90
1344.7Yang, Yuzhu; Yao, Jinzhong; Zhang, Yuhong
Synthesis of polysubstituted furans via copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids.
Organic letters, 2013, 15, 3206-3209
1556155 CIFC20 H21 Cl N O RhP b c a15.6316; 14.9322; 15.632
90; 90; 90
3648.7Zhou, Bing; Du, Juanjuan; Yang, Yaxi; Li, Yuanchao
Rhodium(III)-catalyzed intermolecular direct amidation of aldehyde C-H bonds with N-chloroamines at room temperature.
Organic letters, 2013, 15, 2934-2937
1556156 CIFC16 H19 F6 I O6 S2P -17.9401; 11.866; 12.2428
89.151; 82.917; 83.972
1138.35Saito, Akio; Taniguchi, Akihiro; Kambara, Yui; Hanzawa, Yuji
Metal-free [2 + 2 + 1] annulation of alkynes, nitriles, and oxygen atoms: iodine(III)-mediated synthesis of highly substituted oxazoles.
Organic letters, 2013, 15, 2672-2675
1556157 CIFC58 H40 N4P -19.5556; 10.9143; 21.922
95.336; 99.004; 114.209
2028Mutoh, Katsuya; Shima, Kentaro; Yamaguchi, Tetsuo; Kobayashi, Masayuki; Abe, Jiro
Photochromism of a naphthalene-bridged imidazole dimer constrained to the "anti" conformation.
Organic letters, 2013, 15, 2938-2941
1556158 CIFC20 H20 O6P 21 21 2110.0241; 10.2749; 16.6432
90; 90; 90
1714.19Bautista, Elihú; Toscano, Rubén Alfredo; Ortega, Alfredo
Microphyllandiolide, a new diterpene with an unprecedented skeleton from Salvia microphylla.
Organic letters, 2013, 15, 3210-3213
1556159 CIFC21 H20 F N3 OP 1 21 17.1383; 10.6018; 12.0383
90; 102.375; 90
889.876Aillaud, Isabelle; Barber, David M.; Thompson, Amber L.; Dixon, Darren J.
Enantioselective Michael addition/iminium ion cyclization cascades of tryptamine-derived ureas.
Organic letters, 2013, 15, 2946-2949
1556160 CIFC23 H35 Cl2 F N2 O3 SiP -19.2544; 10.1036; 14.037
89.263; 76.663; 84.842
1271.89Shupe, Benjamin H.; Allen, Emily E.; MacDonald, Jacob P.; Wilson, Sean O.; Franz, Annaliese K.
Synthesis of spirocarbamate oxindoles via intramolecular trapping of a β-silyl carbocation by an N-Boc group.
Organic letters, 2013, 15, 3218-3221
1556161 CIFC12 H9 Cl O4P 1 21/c 19.5934; 34.977; 6.9856
90; 111.154; 90
2186.1Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556162 CIFC24 H22 O6P 6519.1393; 19.1393; 10.2697
90; 90; 120
3257.92Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556163 CIFC13 H12 O5P 1 21/n 18.0607; 12.2714; 11.6095
90; 91.224; 90
1148.1Albertshofer, Klaus; Tan, Bin; Barbas, 3rd, Carlos F
Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions.
Organic letters, 2013, 15, 2958-2961
1556164 CIFC36 H40 Si3P -19.8245; 10.2504; 17.1303
98.958; 106.078; 97.745
1608.4Kinoshita, Hidenori; Takahashi, Hirotoshi; Miura, Katsukiyo
Regioselective synthesis of multisubstituted benzenes by palladium-catalyzed intermolecular reaction of β-iodo-β-silylstyrenes with alkynes.
Organic letters, 2013, 15, 2962-2965
1556165 CIFC37 H30 SiP 1 21/n 110.6578; 14.5155; 39.626
90; 91.372; 90
6128.5Kinoshita, Hidenori; Takahashi, Hirotoshi; Miura, Katsukiyo
Regioselective synthesis of multisubstituted benzenes by palladium-catalyzed intermolecular reaction of β-iodo-β-silylstyrenes with alkynes.
Organic letters, 2013, 15, 2962-2965
1556166 CIFC17 H24 N2 O SiP 1 21/n 113.2419; 8.6081; 15.4864
90; 109.76; 90
1661.3Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556167 CIFC16 H28 N2 O3 SiP 21 21 216.6646; 8.5137; 30.7646
90; 90; 90
1745.6Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556168 CIFC21 H30 N2 O SiP 1 21/c 18.4425; 13.9418; 17.4523
90; 91.014; 90
2053.9Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556169 CIFC12 H20 N2 O SiP 1 21 16.1243; 7.9668; 12.884
90; 98.931; 90
621Liu, Huaqing; O'Connor, Matthew J; Sun, Chunrui; Wink, Donald J.; Lee, Daesung
Sequential reactions of trimethylsilyldiazomethane with 4-alkenyl ketones and aldehydes catalyzed by Lewis bases.
Organic letters, 2013, 15, 2974-2977
1556170 CIFC16 H10 N2 O2P 1 21/n 17.49; 14.7964; 11.472
90; 107.785; 90
1210.6Wang, Chen; Zhang, Lianpeng; Ren, Anni; Lu, Ping; Wang, Yanguang
Cu-catalyzed synthesis of tryptanthrin derivatives from substituted indoles.
Organic letters, 2013, 15, 2982-2985
1556171 CIFC27 H24 O3 SP -18.856; 11.3252; 12.3448
109.775; 92.023; 112.173
1059.92Chang, Meng-Yang; Wu, Ming-Hao; Chen, Yeh-Long
One-pot synthesis of substituted tetrahydrocyclobuta[a]naphthalenes by domino aldol condensation/olefin migration/electrocyclization.
Organic letters, 2013, 15, 2822-2825
1556172 CIFC19 H23 N OP 1 21 16.1008; 7.6894; 17.0974
90; 99.543; 90
790.97Hansmann, Max M.; Hashmi, A Stephen K; Lautens, Mark
Gold meets rhodium: tandem one-pot synthesis of β-disubstituted ketones via Meyer-Schuster rearrangement and asymmetric 1,4-addition.
Organic letters, 2013, 15, 3226-3229
1556173 CIFC23 H21 Br OP 21 21 2110.0001; 10.0316; 19.1693
90; 90; 90
1923.01Hansmann, Max M.; Hashmi, A Stephen K; Lautens, Mark
Gold meets rhodium: tandem one-pot synthesis of β-disubstituted ketones via Meyer-Schuster rearrangement and asymmetric 1,4-addition.
Organic letters, 2013, 15, 3226-3229
1556174 CIFC21 H21 N O2P 1 21/c 19.4044; 19.072; 18.984
90; 101.853; 90
3332.4Chen, Te-Yu; Krische, Michael J.
Regioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: prenylation, geranylation, and beyond.
Organic letters, 2013, 15, 2994-2997
1556175 CIFC17 H16 N2 O3 SP 1 21/c 112.587; 8.748; 14.954
90; 90.12; 90
1646.6Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556176 CIFC25 H19 N3 O3C 1 2/c 118.0952; 10.2372; 21.8977
90; 94.54; 90
4043.7Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556177 CIFC25 H20 N2 OP 1 21/c 111.075; 10.665; 16.846
90; 100.97; 90
1953.4Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556178 CIFC23 H21 N O SP -18.957; 12.165; 17.911
90.195; 104.25; 90.15
1891.5Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556179 CIFC20 H18 N2 O2P 1 21/c 113.639; 10.357; 12.061
90; 106.519; 90
1633.4Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda
Auxiliary-enabled Pd-catalyzed direct arylation of methylene C(sp3)-H bond of cyclopropanes: highly diastereoselective assembling of di- and trisubstituted cyclopropanecarboxamides.
Organic letters, 2013, 15, 3238-3241
1556180 CIFC24 H19 N3 O3P -19.0832; 10.4022; 11.9282
69; 81.227; 83.991
1038.34Ramachary, D. B.; Venkaiah, Chintalapudi; Madhavachary, R.
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis.
Organic letters, 2013, 15, 3042-3045
1556181 CIFC21 H12 Cl N3 O2P 21 21 216.7978; 13.7806; 19.1936
90; 90; 90
1798.01Ramachary, D. B.; Venkaiah, Chintalapudi; Madhavachary, R.
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis.
Organic letters, 2013, 15, 3042-3045
1556182 CIFC28 H22 O4P 1 21/c 114.431; 8.092; 36.817
90; 91.972; 90
4297Li, Erqing; Huang, You; Liang, Ling; Xie, Peizhong
Phosphine-catalyzed [4 + 2] annulation of γ-substituent allenoates: facile access to functionalized spirocyclic skeletons.
Organic letters, 2013, 15, 3138-3141
1556183 CIFC20 H32 O5P 43 21 29.653; 9.653; 40.391
90; 90; 90
3763.6Zhang, Mengke; Zhu, Yan; Zhan, Guanqun; Shu, Penghua; Sa, Rongjian; Lei, Liang; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Wan, Qian; Yao, Guangmin; Zhang, Yonghui
Micranthanone A, a new diterpene with an unprecedented carbon skeleton from Rhododendron micranthum.
Organic letters, 2013, 15, 3094-3097
1556184 CIFC31 H44 O9P 21 21 219.2161; 14.354; 21.9606
90; 90; 90
2905.12Zhang, Mengke; Zhu, Yan; Zhan, Guanqun; Shu, Penghua; Sa, Rongjian; Lei, Liang; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Wan, Qian; Yao, Guangmin; Zhang, Yonghui
Micranthanone A, a new diterpene with an unprecedented carbon skeleton from Rhododendron micranthum.
Organic letters, 2013, 15, 3094-3097
1556185 CIFC17 H17 Br O4P -16.1044; 9.3857; 14.7205
78.9278; 79.0335; 82.9068
809.27Woodall, Erica L.; Simanis, Justin A.; Hamaker, Christopher G.; Goodell, John R.; Mitchell, T. Andrew
Unique reactivity of anti- and syn-acetoxypyranones en route to oxidopyrylium intermediates leading to a cascade process.
Organic letters, 2013, 15, 3270-3273
1556186 CIFC37 H40 Cl N5 O2P 21 21 219.439; 13.768; 26.584
90; 90; 90
3455Zou, Liwei; Wang, Baomin; Mu, Hongfang; Zhang, Huanrui; Song, Yuming; Qu, Jingping
Development of tartaric acid derived chiral guanidines and their application to catalytic enantioselective α-hydroxylation of β-dicarbonyl compounds.
Organic letters, 2013, 15, 3106-3109
1556187 CIFC34 H26 F N O4 S2P 1 21 19.5437; 15.151; 10.6193
90; 111.641; 90
1427.3Matsuzaki, Kohei; Furukawa, Tatsuya; Tokunaga, Etsuko; Matsumoto, Takashi; Shiro, Motoo; Shibata, Norio
Highly enantioselective monofluoromethylation of C2-arylindoles using FBSM under chiral phase-transfer catalysis.
Organic letters, 2013, 15, 3282-3285
1556188 CIFC40.6 H39.25 Cl0.35 F5 N1.5 O4P -16.872; 22.864; 25.039
70.46; 85.66; 76.63
3607Ito, Satoru; Hiroto, Satoru; Shinokubo, Hiroshi
Synthesis of pyridine-fused perylene imides with an amidine moiety for hydrogen bonding.
Organic letters, 2013, 15, 3110-3113
1556189 CIFC24 H26 O4P 1 21 16.2434; 8.0127; 21.1301
90; 90.262; 90
1057.05Ni, Shengjun; Chen, Jie; Ma, Shengming
Unexpected regioselectivity switch: organophosphine-triggered reactions of cyclopropene-1,1-dicarboxylates with aldehydes.
Organic letters, 2013, 15, 3290-3293
1556190 CIFC28 H33 B O2 SiP -110.0966; 10.7209; 13.1753
94.573; 94.171; 109.28
1334.4Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556191 CIFC28 H40 B2 O4 SiP -19.6731; 12.2468; 13.2905
106.215; 91.906; 104.067
1457.8Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556192 CIFC29 H20 F3 N OP -110.299; 12.07; 19.582
89.885; 86.412; 78.391
2379.6Jiao, Jiao; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of multisubstituted olefins through regio- and stereoselective silylborylation of an alkynylboronate/chemoselective cross-coupling sequences.
Organic letters, 2013, 15, 3294-3297
1556193 CIFC30 H26 Br2 O5P 1 21/n 19.8739; 19.0209; 13.9849
90; 94.282; 90
2619.2Yeom, Hyun-Suk; Li, Hui; Tang, Yu; Hsung, Richard P.
Total syntheses of cannabicyclol, clusiacyclol A and B, iso-eriobrucinol A and B, and eriobrucinol.
Organic letters, 2013, 15, 3130-3133
1556194 CIFC16 H20 O3F d d 224.479; 35.736; 6.333
90; 90; 90
5540Yeom, Hyun-Suk; Li, Hui; Tang, Yu; Hsung, Richard P.
Total syntheses of cannabicyclol, clusiacyclol A and B, iso-eriobrucinol A and B, and eriobrucinol.
Organic letters, 2013, 15, 3130-3133
1556195 CIFC16 H10 F3 NP 1 21/c 114.393; 4.9376; 17.802
90; 101.306; 90
1240.6Tiwari, Virendra Kumar; Pawar, Govind Goroba; Das, Riki; Adhikary, Amit; Kapur, Manmohan
Heteroatom-guided, palladium-catalyzed regioselective C-H functionalization in the synthesis of 3-arylquinolines.
Organic letters, 2013, 15, 3310-3313
1556196 CIFC29 H31 B N2 O2P 1 c 111.3125; 9.5581; 12.1929
90; 111.496; 90
1226.66Shaban Ragab, Sherif; Swaminathan, Subramani; Deniz, Erhan; Captain, Burjor; Raymo, Françisco M
Fluorescence photoactivation by ligand exchange around the boron center of a BODIPY chromophore.
Organic letters, 2013, 15, 3154-3157
1556197 CIFC18 H16 N2 O2P 1 21/c 111.1596; 9.7432; 13.8929
90; 102.558; 90
1474.44Chun, Yu Sung; Xuan, Zi; Kim, Ju Hyun; Lee, Sang-gi
An expedient and divergent tandem one-pot synthesis of pyrimidin-2,4-diones using the Blaise reaction intermediate.
Organic letters, 2013, 15, 3162-3165
1556198 CIFC20 H20 O3 SP 1 21 18.1366; 12.602; 9.5079
90; 110.672; 90
912.15Shirakawa, Seiji; Tokuda, Takashi; Kasai, Atsuyuki; Maruoka, Keiji
Design of chiral bifunctional quaternary phosphonium bromide catalysts possessing an amide moiety.
Organic letters, 2013, 15, 3350-3353
1556199 CIFC14 H14 F3 N O5P 1 21/c 19.0022; 12.1545; 13.6525
90; 101.948; 90
1461.46Molander, Gary A.; Cavalcanti, Livia N.
Synthesis of trifluoromethylated isoxazolidines: 1,3-dipolar cycloaddition of nitrosoarenes, (trifluoromethyl)diazomethane, and alkenes.
Organic letters, 2013, 15, 3166-3169
1556200 CIFC23 H18 F3 N O2P 1 21/c 120.4457; 19.4232; 9.4746
90; 90.583; 90
3762.4Molander, Gary A.; Cavalcanti, Livia N.
Synthesis of trifluoromethylated isoxazolidines: 1,3-dipolar cycloaddition of nitrosoarenes, (trifluoromethyl)diazomethane, and alkenes.
Organic letters, 2013, 15, 3166-3169
1556201 CIFC11 H9 N O3P 1 21/c 17.2107; 11.437; 11.361
90; 98.05; 90
927.7Maity, Soham; Naveen, Togati; Sharma, Upendra; Maiti, Debabrata
Stereoselective nitration of olefins with (t)BuONO and TEMPO: direct access to nitroolefins under metal-free conditions.
Organic letters, 2013, 15, 3384-3387
1556202 CIFC100 H150 Cl4 P4P 1 21/n 122.2024; 16.1149; 27.8962
90; 103.284; 90
9713.9Ito, Shigekazu; Kobayashi, Makoto; Mikami, Koichi
Through-space electrostatic interaction between the electron-donating 1,3-diphosphacyclobutane-2,4-diyl units.
Organic letters, 2013, 15, 3404-3407
1556203 CIFC25 H42 O5 SiP 1 21/c 124.5119; 11.5268; 10.5087
90; 120.735; 90
2552.1Kreuzer, Andreas; Kerres, Sabine; Ertl, Thomas; Rücker, Hannelore; Amslinger, Sabine; Reiser, Oliver
Asymmetric synthesis of both enantiomers of arteludovicinolide A.
Organic letters, 2013, 15, 3420-3423
1556204 CIFC23 H38 O5 SiP 21 21 218.16912; 14.1495; 20.6305
90; 90; 90
2384.66Kreuzer, Andreas; Kerres, Sabine; Ertl, Thomas; Rücker, Hannelore; Amslinger, Sabine; Reiser, Oliver
Asymmetric synthesis of both enantiomers of arteludovicinolide A.
Organic letters, 2013, 15, 3420-3423
1556205 CIFC16 H21 Cl N2 O3P 21 21 219.8721; 10.1397; 16.1579
90; 90; 90
1617.4Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
Enantioselective hydroarylation of bridged [3.2.1] heterocycles: an efficient entry into the homoepibatidine skeleton.
Organic letters, 2013, 15, 3424-3427
1556206 CIFC16 H21 Cl N2 O3P 21 21 219.9446; 10.3967; 16.1629
90; 90; 90
1671.1Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
Enantioselective hydroarylation of bridged [3.2.1] heterocycles: an efficient entry into the homoepibatidine skeleton.
Organic letters, 2013, 15, 3424-3427
1556207 CIFC26 H25 N3 O3P -17.5683; 11.9057; 14.1137
102.206; 101.521; 92.584
1212.9Lee, Boram; Chen, Shiyu; Heinis, Christian; Scopelliti, Rosario; Severin, Kay
Pattern-based sensing of peptides and aminoglycosides with a single molecular probe.
Organic letters, 2013, 15, 3456-3459
1556208 CIFC38 H41 N5 O3P -110.1792; 11.8174; 13.9668
90.426; 90.494; 102.848
1637.9Lee, Boram; Chen, Shiyu; Heinis, Christian; Scopelliti, Rosario; Severin, Kay
Pattern-based sensing of peptides and aminoglycosides with a single molecular probe.
Organic letters, 2013, 15, 3456-3459
1556209 CIFC27 H22 N2C 1 2/c 135.073; 8.211; 14.159
90; 106.809; 90
3903.4Zhu, Xu; Wang, Yi-Feng; Ren, Wei; Zhang, Feng-Lian; Chiba, Shunsuke
TEMPO-mediated aliphatic C-H oxidation with oximes and hydrazones.
Organic letters, 2013, 15, 3214-3217
1556210 CIFC28 H22 N2 OP -110.7757; 11.1883; 19.7287
80.672; 74.688; 68.604
2130.3Zhu, Xu; Wang, Yi-Feng; Ren, Wei; Zhang, Feng-Lian; Chiba, Shunsuke
TEMPO-mediated aliphatic C-H oxidation with oximes and hydrazones.
Organic letters, 2013, 15, 3214-3217
1556211 CIFC24 H24 N2 O5 SP 1 21 110.107; 6.8488; 16.9251
90; 90.667; 90
1171.49Meninno, Sara; Croce, Gianluca; Lattanzi, Alessandra
Asymmetric synthesis of trisubstituted tetrahydrothiophenes bearing a quaternary stereocenter via double Michael reaction involving dynamic kinetic resolution.
Organic letters, 2013, 15, 3436-3439
1556212 CIFC28 H33 N O3 SP -111.835; 11.975; 12.118
61.205; 84.631; 63.739
1334Meninno, Sara; Croce, Gianluca; Lattanzi, Alessandra
Asymmetric synthesis of trisubstituted tetrahydrothiophenes bearing a quaternary stereocenter via double Michael reaction involving dynamic kinetic resolution.
Organic letters, 2013, 15, 3436-3439
1556213 CIFC13 H8 N2 O2P b c a12.6783; 7.099; 23.032
90; 90; 90
2073Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556214 CIFC17 H18 Br N2 Na O5P 1 21/c 113.7372; 18.5165; 7.4853
90; 97.958; 90
1885.66Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556215 CIFC14 H10 N2 O3P -17.3116; 15.2786; 16.3552
105.854; 95.436; 95.125
1736.9Slowinski, Franck; Ben Ayad, Omar; Ziyaret, Ozge; Botuha, Candice; Le Falher, Laetitia; Aouane, Kamel; Thorimbert, Serge
Expeditive access to 2-substituted 4H-pyrido[1,3]oxazin-4-ones via an intramolecular O-arylation.
Organic letters, 2013, 15, 3494-3497
1556216 CIFC28 H23 N O3P -18.584; 11.098; 12.526
71.237; 74.269; 80.711
1083.9Yang, Min; Tang, Jie; Fan, Renhua
Dearomatization strategy of β-enamino ester: construction of indenoazepines via tandem Michael addition/polycyclization.
Organic letters, 2013, 15, 3464-3467
1556217 CIFC30 H29 N O5 SP 1 21/c 119.519; 7.83; 18.538
90; 114.675; 90
2574.5Yang, Min; Tang, Jie; Fan, Renhua
Dearomatization strategy of β-enamino ester: construction of indenoazepines via tandem Michael addition/polycyclization.
Organic letters, 2013, 15, 3464-3467
1556218 CIFC10 H12 N2 O3P b c a7.4941; 15.8862; 16.1019
90; 90; 90
1916.98de Robillard, Guillaume; Devillers, Charles H.; Kunz, Doris; Cattey, Hélène; Digard, Eric; Andrieu, Jacques
Electrosynthesis of imidazolium carboxylates.
Organic letters, 2013, 15, 4410-4413
1556219 CIFC9 H13 Cl N2 OP 1 21/c 18.6471; 16.9091; 7.308
90; 111.426; 90
994.69de Robillard, Guillaume; Devillers, Charles H.; Kunz, Doris; Cattey, Hélène; Digard, Eric; Andrieu, Jacques
Electrosynthesis of imidazolium carboxylates.
Organic letters, 2013, 15, 4410-4413
1556220 CIFC32 H37 Br O5P 21 21 216.161; 19.878; 23.992
90; 90; 90
2938.3Ma, Shuang-Gang; Gao, Rong-Mei; Li, Yu-Huan; Jiang, Jian-Dong; Gong, Ning-Bo; Li, Li; Lü, Yang; Tang, Wen-Zhao; Liu, Yun-Bao; Qu, Jing; Lü, Hai-Ning; Li, Yong; Yu, Shi-Shan
Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum.
Organic letters, 2013, 15, 4450-4453
1556221 CIFC32 H37 Br O5P 15.9898; 9.7098; 12.2465
90.307; 91.544; 99.152
702.9Ma, Shuang-Gang; Gao, Rong-Mei; Li, Yu-Huan; Jiang, Jian-Dong; Gong, Ning-Bo; Li, Li; Lü, Yang; Tang, Wen-Zhao; Liu, Yun-Bao; Qu, Jing; Lü, Hai-Ning; Li, Yong; Yu, Shi-Shan
Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum.
Organic letters, 2013, 15, 4450-4453

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