Crystallography Open Database

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Searching journal of publication like 'Organic Letters'

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1555402 CIFC22 H15 Cl OP -16.5461; 8.998; 14.2101
92.224; 101.253; 92.809
818.92Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555403 CIFC22 H15 Br OP 1 21/c 16.253; 15.418; 17.593
90; 92.18; 90
1694.9Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555404 CIFC22 H16 OP 1 21/c 116.0902; 5.6098; 17.2424
90; 94.43; 90
1551.7Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy
Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.
Organic letters, 2015, 17, 5448-5451
1555405 CIFC23 H22 Cl N O4P 21 21 225.273; 6.4369; 12.9596
90; 90; 90
2108.3Liu, Hua-Chao; Liu, Kang; Xue, Zhi-Yong; He, Zhao-Lin; Wang, Chun-Jiang
Silver(I)-Catalyzed Enantioselective Desymmetrization of Cyclopentenediones: Access to Highly Functionalized Bicyclic Pyrrolidines.
Organic letters, 2015, 17, 5440-5443
1555406 CIFC17 H15 N O6 SP 1 21 17.5529; 11.091; 10.123
90; 104.11; 90
822.4Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555407 CIFC24 H21 N O6 SP 21 21 217.7963; 11.5859; 23.086
90; 90; 90
2085.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555408 CIFC18 H15 Br2 Cl2 N O5 SP 1 21 111.974; 5.7044; 15.451
90; 95.49; 90
1050.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555409 CIFC20 H19 N O5 SP 21 21 217.7017; 8.4118; 27.288
90; 90; 90
1767.9Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555410 CIFC17 H14 N4 O5 SP 1 21 18.3457; 10.924; 9.879
90; 109.46; 90
849.2Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555411 CIFC17 H14 Br N O5 SP 1 21 18.091; 6.973; 15.224
90; 101.811; 90
840.7Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555412 CIFC17 H12 Br F2 N O5 SP 21 21 216.8957; 12.551; 22.629
90; 90; 90
1958.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555413 CIFC21 H17 N O5 S2C 2 2 2111.289; 10.612; 32.425
90; 90; 90
3884.5Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555414 CIFC19 H17 Br Cl N O5 SP 21 21 219.155; 9.47; 23.095
90; 90; 90
2002.3Li, Zequan; Shi, Yian
Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.
Organic letters, 2015, 17, 5752-5755
1555415 CIFC14 H22 O4P 21 21 216.5953; 9.079; 21.403
90; 90; 90
1281.6Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555416 CIFC18 H28 O4 SiP 21 21 217.2691; 11.4811; 21.668
90; 90; 90
1808.4Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555417 CIFC15 H18 O7P 1 21 17.187; 8.7702; 11.015
90; 98.176; 90
687.23Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.
Organic letters, 2015, 17, 5480-5483
1555418 CIFC17 H16 F6 O9P 1 21/c 113.5602; 8.6298; 17.3709
90; 92.1; 90
2031.4Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555419 CIFC11 H17 O5P 1 21/n 16.4697; 11.6627; 16.0124
90; 93.278; 90
1206.23Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555420 CIFC17 H19 F3 O9P 1 21/c 113.9325; 8.4366; 16.9502
90; 92.536; 90
1990.4Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.
Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.
Organic letters, 2015, 17, 5760-5763
1555421 CIFC24 H31 N O5 SP 21 21 215.8376; 10.6992; 37.5454
90; 90; 90
2345Serpier, Fabien; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Access to Polyfunctionalized Chiral Piperidines through Enantioselective Addition-Carbocyclization Cascade Reaction Catalyzed by a Rhodium(I)-Diene Complex.
Organic letters, 2015, 17, 5496-5499
1555422 CIFC16 H18 Li N2 OP b c n15.9311; 9.7436; 9.2498
90; 90; 90
1435.81Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555423 CIFC28 H32 N2 Si2P 1 21/c 18.4866; 18.1483; 16.7017
90; 97.928; 90
2547.8Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555424 CIFC44 H62 Li2 N4 O2C 1 2/c 126.34; 11.0689; 18.748
90; 134.32; 90
3910.7Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555425 CIFC39 H46 N2 Si2P c a 2113.9869; 12.5966; 19.4789
90; 90; 90
3431.9Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.
Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.
Organic letters, 2015, 17, 6154-6157
1555426 CIFC13 H15 B F N O5P 1 21/c 113.4038; 9.8242; 11.011
90; 110.376; 90
1359.2St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.
Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.
Organic letters, 2015, 17, 5764-5767
1555427 CIFC15.5 H20 B N2 O7.5 SP 1 21/c 110.3226; 15.7804; 11.1047
90; 107.792; 90
1722.38St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.
Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.
Organic letters, 2015, 17, 5764-5767
1555428 CIFC15 H12 Cl2 O S2P n m a6.9371; 9.8082; 22.3442
90; 90; 90
1520.31Huang, Xin; Wang, Jichao; Ni, Zhangqin; Wang, Sichang; Pan, Yuanjiang
Synthesis of α,α-Disulfenylated Aldehydes via Oxidative Transformation of Tertiary Amines.
Organic letters, 2015, 17, 5488-5491
1555429 CIFC82 H54 N4P -110.1789; 11.9937; 13.2135
108.6; 95.189; 102.354
1471.38Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang
Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.
Organic letters, 2015, 17, 6138-6141
1555430 CIFC82 H54 N4P -110.0347; 11.9855; 25.329
77.339; 87.855; 87.767
2968.7Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang
Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.
Organic letters, 2015, 17, 6138-6141
1555431 CIFC20 H15 Cl N2 O5P 1 21 112.275; 11.187; 13.371
90; 104.835; 90
1774.9Gao, Hang; Luo, Zhenli; Ge, Pingjin; He, Junqian; Zhou, Feng; Zheng, Peipei; Jiang, Jun
Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid.
Organic letters, 2015, 17, 5962-5965
1555432 CIFC25.5 H31 Cl1.5 N2 O5 P SP 1 21 113.5437; 13.0346; 16.0277
90; 102.411; 90
2763.4Kayal, Satavisha; Mukherjee, Santanu
Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates.
Organic letters, 2015, 17, 5508-5511
1555433 CIFC19 H18 F3 N O2 SP 1 c 18.9711; 9.9056; 10.1296
90; 94.135; 90
897.8Zhu, Zi-Zhong; Chen, Kai; Yu, Liu-Zhu; Tang, Xiang-Ying; Shi, Min
Copper(I)-Catalyzed Intramolecular Trifluoromethylation of Methylenecyclopropanes.
Organic letters, 2015, 17, 5994-5997
1555434 CIFC40 H20 O3P 1 21/c 17.63737; 22.5914; 15.1095
90; 99.906; 90
2568.11Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555435 CIFC22 H16 O4P n a 2123.0883; 8.2485; 17.6035
90; 90; 90
3352.5Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555436 CIFC24 H24 N4 O3C 1 2 137.9789; 14.5891; 21.4715
90; 119.848; 90
10318.8Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai
One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.
Organic letters, 2015, 17, 5816-5819
1555437 CIFC25 H28 N4 O5P 21 21 218.2785; 9.2956; 29.7576
90; 90; 90
2289.96Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai
One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.
Organic letters, 2015, 17, 5816-5819
1555438 CIFC44 H63 N5 O11P 1 21/c 119.5349; 6.5541; 34.67
90; 95.943; 90
4415.1Tabor, M. Greg; Shenvi, Ryan A.
Synthesis of Lepadiformine Using a Hydroamination Transform.
Organic letters, 2015, 17, 5776-5779
1555439 CIFC15 H15 N OP 1 21 17.0716; 6.6011; 13.3983
90; 92.659; 90
624.76Vita, Maria Victoria; Caramenti, Paola; Waser, Jerome
Enantioselective Synthesis of Homoallylic Azides and Nitriles via Palladium-Catalyzed Decarboxylative Allylation.
Organic letters, 2015, 17, 5832-5835
1555440 CIFC29 H30 Br N3 OP -18.9762; 9.2143; 15.8055
91.311; 97.75; 93.388
1292.4Duan, Xiao-Yong; Yang, Xiu-Long; Jia, Pan-Pan; Zhang, Man; Han, Bing
Hydrazonyl Radical-Participated Tandem Reaction: A Strategy for the Synthesis of Pyrazoline-Functionalized Oxindoles.
Organic letters, 2015, 17, 6022-6025
1555441 CIFC18 H13 N O3P 1 21/n 19.2686; 16.156; 9.4109
90; 95.246; 90
1403.3Sengoku, Tetsuya; Murata, Yusuke; Aso, Yuwa; Kawakami, Ai; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure.
Organic letters, 2015, 17, 5846-5849
1555442 CIFC104 H170 Cl8 Cu2 N16 O17C 1 2/c 125.299; 19.2324; 28.254
90; 91.806; 90
13740Ganss, Alexander; Belda, Raquel; Pitarch, Javier; Goddard, Richard; García-España, Enrique; Kubik, Stefan
Synthesis and Structural Characterization of a Cyclen-Derived Molecular Cage.
Organic letters, 2015, 17, 5850-5853
1555443 CIFC28 H32 Br N3 O3P 1 21/c 116.0245; 8.5681; 19.233
90; 95.076; 90
2630.3Douchez, Antoine; Lubell, William D.
Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.
Organic letters, 2015, 17, 6046-6049
1555444 CIFC20 H15 Br Cl N3 O3P 1 21/n 18.8959; 13.3302; 15.9639
90; 91.132; 90
1892.7Douchez, Antoine; Lubell, William D.
Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.
Organic letters, 2015, 17, 6046-6049
1555445 CIFC24 H21 N5 O2P -18.7322; 9.9954; 12.0561
78.166; 89.574; 82.698
1021.37Ramanathan, Mani; Wang, Yu-Hao; Liu, Shiuh-Tzung
One-Pot Reactions for Synthesis of 2,5-Substituted Tetrazoles from Aryldiazonium Salts and Amidines.
Organic letters, 2015, 17, 5886-5889
1555446 CIFC18 H22 O2P 21 21 219.0068; 10.478; 16.4734
90; 90; 90
1554.65Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei
Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols.
Organic letters, 2015, 17, 6058-6061
1555447 CIFC21 H16 O3P b c a15.108; 7.54; 27.9119
90; 90; 90
3179.6Ravi Kumar, Devarapalli; Satyanarayana, Gedu
Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.
Organic letters, 2015, 17, 5894-5897
1555448 CIFC15 H12 O3P 1 21/n 17.8593; 4.0079; 36.679
90; 93.567; 90
1153.1Ravi Kumar, Devarapalli; Satyanarayana, Gedu
Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.
Organic letters, 2015, 17, 5894-5897
1555449 CIFC20 H30 O2C 1 2 120.0748; 6.8584; 25.9078
90; 106.399; 90
3421.9Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555450 CIFC24 H36 O4P 1 21 111.623; 7.3026; 12.673
90; 95.271; 90
1071.1Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555451 CIFC24 H36 O4C 1 2 131.775; 7.261; 19.184
90; 104.026; 90
4294.1Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555452 CIFC24 H36 O4P 1 21 110.27; 7.257; 14.424
90; 92.479; 90
1074Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555453 CIFC38 H54 O5P 21 21 2110.0955; 13.4185; 24.927
90; 90; 90
3376.8Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.
Organic letters, 2015, 17, 6062-6065
1555454 CIFC62 H84 N8 O2 S2 Si4P -18.2413; 12.7682; 15.6926
80.64; 82.824; 75.922
1574.06Cortizo-Lacalle, Diego; Gozalvez, Cristian; Olano, Mikel; Sun, Xiangnan; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio
Bisthiadiazole-Fused Tetraazapentacenequinone: An Air-Stable Solution-Processable n-Type Organic Semiconductor.
Organic letters, 2015, 17, 5902-5905
1555455 CIFC31 H23 Cl2 N O4 SP -19.8014; 12.1207; 13.323
99.552; 106.402; 111.742
1343.8Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang
Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.
Organic letters, 2015, 17, 6078-6081
1555456 CIFC30 H21 Cl2 N O3 SP -17.3264; 7.7051; 23.332
84.594; 88.837; 82.404
1299.7Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang
Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.
Organic letters, 2015, 17, 6078-6081
1555457 CIFC23 H18 N2 O3 SP -19.5468; 10.4076; 11.3179
103.653; 93.612; 114.414
978.53Qiao, Huijie; Sun, Suyan; Yang, Fan; Zhu, Yu; Zhu, Weiguo; Dong, Yaxi; Wu, Yusheng; Kong, Xiangtao; Jiang, Ling; Wu, Yangjie
Copper(I)-Catalyzed Sulfonylation of 8-Aminoquinoline Amides with Sulfonyl Chlorides in Air.
Organic letters, 2015, 17, 6086-6089
1555458 CIFC56 H40 F6 N6P 1 21/c 17.398; 11.831; 25.874
90; 94.823; 90
2256.6Tasior, Mariusz; Chotkowski, Maciej; Gryko, Daniel T.
Extension of Pyrrolopyrrole π-System: Approach to Constructing Hexacyclic Nitrogen-Containing Aromatic Systems.
Organic letters, 2015, 17, 6106-6109
1555459 CIFC136 H112 OP -110.6194; 15.7603; 16.3359
73.944; 87.761; 73.938
2522.8He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555460 CIFC62.74 H45.48 Cl1.48P -19.9913; 15.4197; 15.7043
102.428; 92.308; 99.776
2321He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555461 CIFC104 H80 OP -110.2023; 12.2529; 16.1191
98.99; 102.37; 105.55
1846.7He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555462 CIFC52 H40 O0.5P -110.11; 10.19; 36.97
91.2; 94.1; 95.6
3779.3He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555463 CIFC58 H52 OC 1 2/c 130.72; 17.174; 16.373
90; 97.824; 90
8557.7He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.
Organic letters, 2015, 17, 6174-6177
1555464 CIFC19 H17 Cl N2 O1.425P 1 21/c 113.0804; 18.104; 15.8995
90; 102.512; 90
3675.7Jiang, Pingping; Li, Feng; Xu, Yongbao; Liu, Qingwen; Wang, Jing; Ding, Hong; Yu, Renfu; Wang, Qifeng
Aromaticity-Dependent Regioselectivity in Pd(II)-Catalyzed C-H Direct Arylation of Aryl Ureas.
Organic letters, 2015, 17, 5918-5921
1555465 CIFC21 H14 O4P n a 219.2786; 23.641; 7.5289
90; 90; 90
1651.5Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555466 CIFC15 H12 O3P 1 21/n 113.899; 6.5834; 14.579
90; 117.751; 90
1180.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555467 CIFC20 H14 O2P 21 21 217.3238; 9.814; 19.747
90; 90; 90
1419.3Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555468 CIFC14 H10 O3P 1 21/n 110.271; 9.1771; 11.2051
90; 97.686; 90
1046.7Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555469 CIFC22 H14 O3P b c a12.5409; 7.8473; 31.588
90; 90; 90
3108.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555470 CIFC19 H14 O3P -16.866; 10.24; 11.188
69.311; 72.734; 83.093
702.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555471 CIFC17 H13 N O3P 1 21/c 14.629; 16.421; 17.474
90; 91.158; 90
1328Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555472 CIFC18 H12 O3P -17.4224; 7.787; 12.133
99.775; 91.453; 97.925
683.6Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong
Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.
Organic letters, 2015, 17, 5926-5929
1555473 CIFC21 H19 N O5P 1 21/c 19.3725; 21.712; 9.3146
90; 106.094; 90
1821.2Hong, Jung-Ho; Atta, Ananta Kumar; Jung, Kwang-Bok; Kim, Seul-Bi; Heo, Jungseok; Cho, Dong-Gyu
Conformationally Locked Tolans, β-Sheet Structures, and Photophysical Properties.
Organic letters, 2015, 17, 6222-6225
1555474 CIFC17 H22 N O3 SP 1 21 18.5345; 8.8037; 11.0062
90; 90.369; 90
826.94Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.
Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.
Organic letters, 2015, 17, 6226-6229
1555475 CIFC13 H18 N3 O4P 1 21 16.1187; 15.5628; 7.4298
90; 90.617; 90
707.46Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.
Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.
Organic letters, 2015, 17, 6226-6229
1555476 CIFC10 H20 O S2 SiP 1 21 16.642; 14.2879; 13.6807
90; 91.605; 90
1297.79Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B
An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.
Organic letters, 2015, 17, 6242-6245
1555477 CIFC18 H34 O S4 SiP -19.7683; 10.4783; 12.5293
102.548; 99.034; 115.038
1088.3Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B
An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.
Organic letters, 2015, 17, 6242-6245
1555478 CIFC23 H21 N OP 1 21/c 112.2975; 14.2131; 10.3046
90; 107.61; 90
1716.7Taguchi, Masamitsu; Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki
Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group.
Organic letters, 2015, 17, 6250-6253
1555479 CIFC24 H8 Br2 N2P 1 21/n 111.5512; 7.5173; 22.879
90; 91.554; 90
1985.9Min, Lijun; Pan, Bin; Gu, Yanlong
Synthesis of Quinoline-Fused 1-Benzazepines through a Mannich-Type Reaction of a C,N-Bisnucleophile Generated from 2-Aminobenzaldehyde and 2-Methylindole.
Organic letters, 2016, 18, 364-367
1555480 CIFC21 H18 Br NP 1 21 110.094; 14.285; 11.689
90; 90.952; 90
1685.2Zhang, Zhenhua; Du, Haifeng
Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines.
Organic letters, 2015, 17, 6266-6269
1555481 CIFC24 H24 N2 O2P 1 21/c 19.0073; 29.18; 7.8919
90; 104.587; 90
2007.39Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.
Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.
Organic letters, 2015, 17, 6270-6273
1555482 CIFC24 H24 N2 OP -110.369; 13.94; 14.494
83.533; 85.279; 75.051
2008.1Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.
Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.
Organic letters, 2015, 17, 6270-6273
1555483 CIFC25 H30 N2 O5P 1 21 18.73; 13.8357; 9.1173
90; 93.75; 90
1098.88Zhang, Hua; Zhu, Kong-Kai; Han, Ying-Shan; Luo, Cheng; Wainberg, Mark A.; Yue, Jian-Min
Flueggether A and Virosinine A, Anti-HIV Alkaloids from Flueggea virosa.
Organic letters, 2015, 17, 6274-6277
1555484 CIFC16 H24 N3 O3 PP b c a28.26; 11.505; 11.128
90; 90; 90
3618Ahamad, Shakir; Kant, Ruchir; Mohanan, Kishor
Metal-Free Three-Component Domino Approach to Phosphonylated Triazolines and Triazoles.
Organic letters, 2016, 18, 280-283
1555485 CIFC22 H13 Cl F N3 O SP n a 2117.7894; 18.2676; 5.7336
90; 90; 90
1863.2Fan, Wei; Li, Qun; Li, Yanrong; Sun, Hao; Jiang, Bo; Li, Guigen
I2/O2-Enabled N-S Bond Formation to Access Functionalized 1,2,3-Thiadiazoles.
Organic letters, 2016, 18, 1258-1261
1555486 CIFC25 H19.78 N3 O2.39 PdP -18.4976; 11.7441; 20.5928
80.687; 83.765; 78.031
1977.91Wiest, Johannes M.; Pöthig, Alexander; Bach, Thorsten
Pyrrole as a Directing Group: Regioselective Pd(II)-Catalyzed Alkylation and Benzylation at the Benzene Core of 2-Phenylpyrroles.
Organic letters, 2016, 18, 852-855
1555487 CIFC20 H21 N O2P b c a14.6593; 7.8044; 27.406
90; 90; 90
3135.4Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555488 CIFC17 H17 N O SP 1 21/c 18.6142; 9.0565; 18.42
90; 103.352; 90
1398.18Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555489 CIFC15 H17 N OP 1 21/n 114.5023; 8.2306; 20.0369
90; 98.744; 90
2363.9Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555490 CIFC19 H19 N OP b c a13.21; 7.8624; 27.4014
90; 90; 90
2846Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555491 CIFC23 H29 N O4 SP -19.523; 9.6405; 11.7824
83.18; 76.85; 71.05
995.1Murai, Kenichi; Matsuura, Kei; Aoyama, Hiroshi; Fujioka, Hiromichi
Oxidative Rearrangement via in Situ Generated N-Chloroamine: Synthesis of Fused Tetrahydroisoquinolines.
Organic letters, 2016, 18, 1314-1317
1555492 CIFC16 H17 N3 O3P -18.6512; 13.1178; 13.2085
94.755; 97.921; 102.375
1440.34Zhang, Lin-Bao; Zhang, Shou-Kun; Wei, Donghui; Zhu, Xinju; Hao, Xin-Qi; Su, Jian-Hang; Niu, Jun-Long; Song, Mao-Ping
Cobalt(II)-Catalyzed C-H Amination of Arenes with Simple Alkylamines.
Organic letters, 2016, 18, 1318-1321
1555493 CIFC17 H21 NP -16.0723; 8.6709; 14.006
75.45; 78.72; 70.16
666.5Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555494 CIFC19 H33 N O6P 1 21/c 119.714; 6.3466; 16.045
90; 90.8; 90
2007.3Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555495 CIFC24 H22 Br N3 O5.5P 21 21 2112.8376; 12.9227; 14.0967
90; 90; 90
2338.59Kumarswamyreddy, Nandarapu; Kesavan, Venkitasamy
Enantioselective Synthesis of Dihydrospiro[indoline-3,4'-pyrano[2,3-c]pyrazole] Derivatives via Michael/Hemiketalization Reaction.
Organic letters, 2016, 18, 1354-1357
1555496 CIFC25 H22 F N O2P 21 21 219.56524; 18.64102; 22.57118
90; 90; 90
4024.57Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555497 CIFC25 H22 Cl N O2P 1 21 110.8203; 8.0501; 11.8593
90; 90.3984; 90
1032.97Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555498 CIFC88 H89 B3 N6P 1 21/n 19.8983; 28.293; 24.5786
90; 96.552; 90
6838.3Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555499 CIFC45 H51 B3 F6 N6P 1 21/n 116.672; 6.7638; 37.518
90; 99.692; 90
4170.4Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555500 CIFC19 H26 O3P 21 21 216.43415; 13.9695; 18.8234
90; 90; 90
1691.88Lin, Han; Xiao, Li-Jun; Zhou, Min-Jie; Yu, Hong-Ming; Xie, Jian-Hua; Zhou, Qi-Lin
Enantioselective Approach to (-)-Hamigeran B and (-)-4-Bromohamigeran B via Catalytic Asymmetric Hydrogenation of Racemic Ketone To Assemble the Chiral Core Framework.
Organic letters, 2016, 18, 1434-1437
1555501 CIFC20 H20 O7P 1 21/c 113.364; 7.917; 21.513
90; 127.54; 90
1804.8More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555502 CIFC21 H24 O6P 1 21/c 111.9383; 10.2634; 15.2907
90; 97.621; 90
1857More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555503 CIFC11 H12 O3P -17.2646; 8.0955; 8.184
90.831; 97.639; 93.425
476.06More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555504 CIFC33 H37 Cl N2 O6C 1 2/c 125.162; 15.406; 16.174
90; 109.269; 90
5919Di Maso, Michael J.; Nepomuceno, Gabriella M.; St Peter, Michael A.; Gitre, Haley H.; Martin, Kevin S.; Shaw, Jared T.
Synthesis of (±)-Bisavenanthramide B-6 by an Anionic Anhydride Mannich Reaction.
Organic letters, 2016, 18, 1740-1743
1555505 CIFC164 H260 N4 O75 S3P 21 21 2118.0825; 18.5554; 56.7015
90; 90; 90
19024.9Inouye, Masahiko; Yoshizawa, Atsushi; Shibata, Mari; Yonenaga, Yuki; Fujimoto, Kazuhisa; Sakata, Takuma; Matsumoto, Shinya; Shiro, Motoo
Cyclodextrin-Isolated Alkynylpyrenes as UV-Stable and Blue-Light-Emitting Molecules Even in Condensed States.
Organic letters, 2016, 18, 1960-1963
1555506 CIFC13 H18 O1.5P 1 21 110.2913; 7.9908; 13.7239
90; 97.986; 90
1117.65Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555507 CIFC26 H38 O3P 1 21 110.3364; 8.2959; 12.9455
90; 96.995; 90
1101.81Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555508 CIFC18 H21 N O5P 1 21/n 112.4616; 7.5556; 17.8282
90; 109.236; 90
1584.9Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555509 CIFC17 H18 Cl N O5P 21 21 216.891; 11.883; 20.413
90; 90; 90
1671.5Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555510 CIFC23 H23 N O5P 1 21/n 116.5186; 6.7973; 17.4934
90; 97.222; 90
1948.6Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555511 CIFC17 H19 N O5P 21 21 217.7825; 12.1682; 16.9656
90; 90; 90
1606.63Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555512 CIFC26 H22 N3 O2 PP 1 21/c 111.3945; 16.435; 12.4553
90; 107.236; 90
2227.7Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555513 CIFC26 H22 N3 O2 PP 1 21/c 110.704; 21.3272; 11.2625
90; 120.672; 90
2211.4Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555514 CIFC21 H28 O4P 1 21/c 115.5552; 15.6415; 8.1031
90; 94.596; 90
1965.2Elliott, Daniel C.; Ma, Tsz-Kan; Selmani, Aymane; Cookson, Rosa; Parsons, Philip J.; Barrett, Anthony G. M.
Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates.
Organic letters, 2016, 18, 1800-1803
1555515 CIFC19 H16 Cl N O2P 1 21/c 112.568; 7.479; 17.461
90; 108.353; 90
1557.8Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555516 CIFC19 H17 N O2P -18.206; 8.581; 10.584
90.785; 100.066; 104.431
709.4Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555517 CIFC15 H16 O3R -3 :H29.475; 29.475; 7.245
90; 90; 120
5451Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555518 CIFC18 H22 O5P 1 21/n 16.613; 28.29; 8.886
90; 103.404; 90
1617.1Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555519 CIFC13 H15 Br Cl N O2P 1 21/c 110.4382; 24.2507; 10.9589
90; 95.0262; 90
2763.4Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555520 CIFC9 H7 Cl N2P 1 21/c 19.8146; 3.9248; 20.553
90; 103.021; 90
771.35Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555521 CIFC23 H16 F2 N4 O2P 1 21 17.8577; 14.9042; 9.3787
90; 113.529; 90
1007.05Qiao, Jin-Bao; Zhao, Yu-Ming; Gu, Peiming
Asymmetric Intramolecular Desymmetrization of meso-α,α'-Diazido Alcohols with Aryldiazoacetates: Assembly of Chiral C3 Fragments with Three Continuous Stereocenters.
Organic letters, 2016, 18, 1984-1987
1555522 CIFC15 H21 N3 O3P -16.433; 7.542; 15.771
90.874; 95.675; 109.593
716.4Mehr, S Hessam M; Patrick, Brian O.; MacLachlan, Mark J.
Stabilization of a Strained Heteroradialene by Peripheral Electron Delocalization.
Organic letters, 2016, 18, 1840-1843
1555523 CIFC17 H25 Cl F N OP 1 21/c 113.3762; 9.6596; 13.4588
90; 93.8818; 90
1735.01Hamel, Jean-Denys; Cloutier, Mélissa; Paquin, Jean-François
Exploiting a Difference in Leaving Group Ability: An Approach to β-Substituted Monofluoroalkenes Using gem-Chlorofluoropropenes.
Organic letters, 2016, 18, 1852-1855
1555524 CIFC20 H14P 1 21 16.4855; 7.5481; 13.9074
90; 95.824; 90
677.3Zhou, Yujing; Ye, Fei; Zhou, Qi; Zhang, Yan; Wang, Jianbo
Cu(I)-Catalyzed Tandem Reaction of Carbene Coupling and Horner-Wadsworth-Emmons Type Olefination: Access toward Enynes.
Organic letters, 2016, 18, 2024-2027
1555525 CIFC23 H39 N O3 S SiP 21 21 2111.2183; 17.958; 25.733
90; 90; 90
5184.1Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555526 CIFC25 H37 N3 O3P 21 21 218.174; 12.797; 21.823
90; 90; 90
2282.7Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555527 CIFC21 H33 N O5P 21 21 211.42; 19.1624; 9.3685
90; 90; 90
2050.2Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555528 CIFC18 H31 N O5P 21 21 217.71375; 8.88494; 28.0459
90; 90; 90
1922.16Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555529 CIFC21 H31 N O5P 1 21 111.5555; 6.7668; 12.9264
90; 98.846; 90
998.74Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555530 CIFC38 H22P 1 21/n 117.4392; 7.3355; 17.5242
90; 94.296; 90
2235.49Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555531 CIFC36 H18P 1 21/c 112.7866; 3.9237; 42.438
90; 95.156; 90
2120.53Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555532 CIFC15 H11 Br N2 OP 1 21/c 17.5865; 11.136; 15.609
90; 96.63; 90
1309.9Wang, Jie; Zha, Shanke; Chen, Kehao; Zhang, Feifei; Song, Chao; Zhu, Jin
Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C-H Functionalization of Benzimidates with Dioxazolones.
Organic letters, 2016, 18, 2062-2065
1555533 CIFC20 H20 O2 S2P 1 21/n 110.3493; 16.6118; 11.4274
90; 116.111; 90
1764.1Lai, Junshan; Liang, Yongping; Liu, Teng; Tang, Shouchu
Dithiane Induced Cycloaddition/Aromatization Tactic for the Synthesis of Multisubstituted Furans.
Organic letters, 2016, 18, 2066-2069
1555534 CIFC20 H28 N2 O3P 1 21 19.7442; 6.1717; 14.9524
90; 90.609; 90
899.16Hsieh, Sheng-Ying; Bode, Jeffrey W.
Silicon Amine Reagents for the Photocatalytic Synthesis of Piperazines from Aldehydes and Ketones.
Organic letters, 2016, 18, 2098-2101
1555535 CIFC19 H25 Cl N O RhP 1 21/c 113.0578; 15.8566; 18.5108
90; 91.055; 90
3832.1Wang, Qiang; Li, Xingwei
Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis.
Organic letters, 2016, 18, 2102-2105
1555536 CIFC15 H15 Br O3 SP 1 21 15.92604; 12.2676; 9.9444
90; 103.755; 90
702.21Pagire, Santosh K.; Paria, Suva; Reiser, Oliver
Synthesis of β-Hydroxysulfones from Sulfonyl Chlorides and Alkenes Utilizing Visible Light Photocatalytic Sequences.
Organic letters, 2016, 18, 2106-2109
1555537 CIFC46 H39 Au2 F6 N O5 P2 S3P 1 c 114.011; 16.7528; 20.7802
90; 105.001; 90
4711.4Tamai, Taichi; Fujiwara, Keiko; Higashimae, Shinya; Nomoto, Akihiro; Ogawa, Akiya
Gold-Catalyzed Anti-Markovnikov Selective Hydrothiolation of Unactivated Alkenes.
Organic letters, 2016, 18, 2114-2117
1555538 CIFC12 H13 N O2P 1 21/n 19.8079; 8.8394; 12.567
90; 99.596; 90
1074.3Fraboni, Americo J.; Brenner-Moyer, Stacey E
Dienamine-Catalyzed Nitrone Formation via Redox Reaction.
Organic letters, 2016, 18, 2146-2149
1555539 CIFC16 H15 Br Cl3 N O2P -17.5091; 10.1225; 12.5419
76.957; 81.066; 75.302
893.46García-García, Carolina; Ortiz-Rojano, Laura; Álvarez, Susana; Álvarez, Rosana; Ribagorda, María; Carreño, M Carmen
Friedel-Crafts Alkylation of Indoles with p-Quinols: The Role of Hydrogen Bonding of Water for the Desymmetrization of the Cyclohexadienone System.
Organic letters, 2016, 18, 2224-2227
1555540 CIFC17 H11 N OP -13.991; 10.967; 15.118
73.536; 86.417; 81.507
627.5Wang, Lianjie; Liu, Xiaocui; Wang, Mang; Liu, Jun
Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans.
Organic letters, 2016, 18, 2162-2165
1555541 CIFC20 H27 O3.5I 4119.7536; 19.7536; 9.0366
90; 90; 90
3526.1Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555542 CIFC20 H26 O3P 21 21 219.7169; 10.1381; 17.5286
90; 90; 90
1726.76Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555543 CIFC22 H32 O4C 1 2 118.2916; 8.7712; 12.993
90; 103.232; 90
2029.24Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555544 CIFC22 H20 Br N O2P 1 21 18.6651; 5.8524; 18.9495
90; 93.712; 90
958.94Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555545 CIFC24 H25 N O4P 112.7971; 12.8656; 14.0933
88.968; 86.108; 66.582
2124.21Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555546 CIFC28 H25 N O2P 21 21 215.9977; 8.669; 42.0392
90; 90; 90
2185.79Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555547 CIFC40 H40 N2 O SP -110.2707; 12.5581; 14.2615
78.265; 69.761; 81.577
1684Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555548 CIFC26 H25 Cl2 N O4 SP -19.9795; 10.2314; 12.8722
92.489; 106.194; 96.538
1250.1Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555549 CIFC21 H15 NP -110.3062; 11.6276; 13.2088
75.92; 88.72; 87.09
1533.28Saunthwal, Rakesh K.; Patel, Monika; Verma, Akhilesh K.
Metal- and Protection-Free [4 + 2] Cycloadditions of Alkynes with Azadienes: Assembly of Functionalized Quinolines.
Organic letters, 2016, 18, 2200-2203
1555550 CIFC12 H9 F3 N2 OP 1 21/c 19.3458; 13.3878; 9.015
90; 104.592; 90
1091.57Nguyen, Thanh Binh; Ermolenko, Ludmila; Retailleau, Pascal; Al-Mourabit, Ali
Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2016, 18, 2177-2179
1555551 CIFC16 H18 N2 O2P 1 21 18.94706; 11.2291; 14.9983
90; 102.552; 90
1470.83Halskov, Kim Søholm; Næsborg, Line; Tur, Fernando; Jørgensen, Karl Anker
Asymmetric [3 + 2] Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Aldehydes by Synergistic Palladium and Organocatalysis.
Organic letters, 2016, 18, 2220-2223
1555552 CIFC8 H9 Cl N4 OP 21 21 215.3345; 17.4841; 6.9026
90; 90; 90
1850.7Sun, Huan-Li; Chen, Fei; Xie, Ming-Sheng; Guo, Hai-Ming; Qu, Gui-Rong; He, Yan-Mei; Fan, Qing-Hua
Asymmetric Hydrogenation of α-Purine Nucleobase-Substituted Acrylates with Rhodium Diphosphine Complexes: Access to Tenofovir Analogues.
Organic letters, 2016, 18, 2260-2263
1555553 CIFC18 H22 F N O4P 21 21 219.7821; 11.5835; 14.8591
90; 90; 90
1683.7Zhu, Luyi; Chen, Qiliang; Shen, Dan; Zhang, Weihao; Shen, Cong; Zeng, Xiaofei; Zhong, Guofu
Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction.
Organic letters, 2016, 18, 2387-2390
1555554 CIFC28 H24 O6 S2P 1 21/c 116.268; 7.4469; 22.374
90; 110.413; 90
2540.3Ni, Chunjie; Wang, MingLi; Tong, Xiaofeng
Access to Thiophene and 1H-Pyrrole via Amine-Initiated (3 + 2) Annulation and Aromatization Cascade Reaction of β'-Acetoxy Allenoate and 1,2-Bisnucleophile.
Organic letters, 2016, 18, 2240-2243
1555555 CIFC33 H26 Cl N O5 SP 1 21/c 110.2049; 23.693; 12.5597
90; 107.704; 90
2892.9Lv, Leiyang; Li, Zhiping
Iron-Catalyzed Radical [2 + 2 + 2] Annulation of Benzene-Linked 1,7-Enynes with Aldehydes: Fused Pyran Compounds.
Organic letters, 2016, 18, 2264-2267
1555556 CIFC22 H18 Br2 O4P 1 21/n 18.4295; 10.9126; 22.07
90; 90.7067; 90
2030.02Li, Shuangjiang; Huang, Changfeng; Thakellapalli, Haresh; Farajidizaji, Behzad; Popp, Brian V.; Petersen, Jeffrey L.; Wang, Kung K.
Syntheses and Structures of Functionalized [9]Cycloparaphenylenes as Carbon Nanohoops Bearing Carbomethoxy and N-Phenylphthalimido Groups.
Organic letters, 2016, 18, 2268-2271
1555557 CIFC91 H80 Cl2 O12P -114.0233; 16.2794; 19.2082
66.9176; 72.0505; 77.5633
3815.2Li, Shuangjiang; Huang, Changfeng; Thakellapalli, Haresh; Farajidizaji, Behzad; Popp, Brian V.; Petersen, Jeffrey L.; Wang, Kung K.
Syntheses and Structures of Functionalized [9]Cycloparaphenylenes as Carbon Nanohoops Bearing Carbomethoxy and N-Phenylphthalimido Groups.
Organic letters, 2016, 18, 2268-2271
1555558 CIFC24 H20 O2P 1 21/c 111.2926; 12.6823; 13.3977
90; 112.956; 90
1766.8Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Correction to "Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides".
Organic letters, 2016, 18, 2323-2324
1555559 CIFC29 H24 O3P 1 21/c 113.3405; 7.7448; 22.406
90; 104.615; 90
2240.1Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian
Correction to "Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides".
Organic letters, 2016, 18, 2323-2324
1555560 CIFC14 H8 F2 N2 O SP -15.737; 7.6865; 13.5874
88.575; 86.523; 88.004
597.55Castanheiro, Thomas; Suffert, Jean; Gulea, Mihaela; Donnard, Morgan
Aerobic Copper-Mediated Domino Three-Component Approach to 2-Aminobenzothiazole Derivatives.
Organic letters, 2016, 18, 2588-2591
1555561 CIFC20 H17 Br N2 O2P -17.7454; 10.3627; 11.1019
107.48; 90.474; 97.723
841.1Liang, Ling; Huang, You
Phosphine-Catalyzed [3 + 3]-Domino Cycloaddition of Ynones and Azomethine Imines To Construct Functionalized Hydropyridazine Derivatives.
Organic letters, 2016, 18, 2604-2607
1555562 CIFC23 H30 F2 N2 O2P 1 21/n 113.5393; 9.9243; 17.0947
90; 103.566; 90
2232.9Wang, Qiang; He, Yu-Tao; Zhao, Jia-Hui; Qiu, Yi-Feng; Zheng, Lan; Hu, Jing-Yuan; Yang, Yu-Chen; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Regioselective Difluoroalkylation and Carbonylation of Alkynes.
Organic letters, 2016, 18, 2664-2667
1555563 CIFC20 H15 Cl2 N O4 SP 1 21/c 115.368; 8.0607; 16.717
90; 114.31; 90
1887.2Jia, Penghao; Huang, You
Sequential Annulation Domino Reaction of Sulfur Ylides and α,β-Unsaturated Cyclic Ketimines: Synthesis of Cyclic 2-Alkenyl Aziridines.
Organic letters, 2016, 18, 2475-2478
1555564 CIFC16 H24 N2 O3 SP 21 21 218.6938; 9.8115; 18.943
90; 90; 90
1615.8Crossley, Steven W. M.; Martinez, Ruben M.; Guevara-Zuluaga, Sebastián; Shenvi, Ryan A.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Organic letters, 2016, 18, 2620-2623
1555565 CIFC21 H22 N2 O6P -17.7666; 15.5767; 16.2634
91.394; 99.881; 90.214
1937.69Crossley, Steven W. M.; Martinez, Ruben M.; Guevara-Zuluaga, Sebastián; Shenvi, Ryan A.
Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.
Organic letters, 2016, 18, 2620-2623
1555566 CIFC37 H36 F N O5 S2P -18.6308; 13.95; 15.866
102.47; 103.64; 105.496
1707.7Guang, Jie; Rout, Saroj; Bihani, Manisha; Larson, Ariel J.; Arman, Hadi D.; Zhao, John C.-G.
Organocatalyzed Enantioselective Direct Mannich Reaction of α-Styrylacetates.
Organic letters, 2016, 18, 2648-2651
1555567 CIFC20 H17 F5 N2 O5P 1 21/c 15.76; 42.882; 8.034
90; 94.022; 90
1979.5Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555568 CIFC17 H26 N2 O2P 1 21/n 113.2033; 7.3109; 17.144
90; 97.707; 90
1639.9Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555569 CIFC13 H15 Cl F5 N O2P 1 21/n 114.84; 6.9273; 15.2459
90; 109.128; 90
1480.8Luescher, Michael U.; Bode, Jeffrey W.
SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes.
Organic letters, 2016, 18, 2652-2655
1555570 CIFC24 H19 Br N2 O2P 1 21 111.311; 5.661; 16.455
90; 108.595; 90
998.6Winterton, Sarah E.; Ready, Joseph M.
[3 + 2]-Cycloadditions of Azomethine Imines and Ynolates.
Organic letters, 2016, 18, 2608-2611
1555571 CIFC24 H35 N O5P 15.9846; 7.913; 12.691
99.814; 95.953; 107.509
557Nagaraju, Karre; Chegondi, Rambabu; Chandrasekhar, Srivari
Expanding Diversity without Protecting Groups: (+)-Sclareolide to Indolosesquiterpene Alkaloid Mycoleptodiscin A and Analogues.
Organic letters, 2016, 18, 2684-2687
1555572 CIFC25 H34 N2 O4P 21 21 216.0956; 15.5691; 24.6358
90; 90; 90
2338.01Nagaraju, Karre; Chegondi, Rambabu; Chandrasekhar, Srivari
Expanding Diversity without Protecting Groups: (+)-Sclareolide to Indolosesquiterpene Alkaloid Mycoleptodiscin A and Analogues.
Organic letters, 2016, 18, 2684-2687
1555573 CIFC23 H21 B N2 O2P 1 21/n 111.7488; 11.331; 16.0382
90; 110.789; 90
1996.09Mazzanti, Andrea; Mercanti, Elia; Mancinelli, Michele
Axial Chirality about Boron-Carbon Bond: Atropisomeric Azaborines.
Organic letters, 2016, 18, 2692-2695
1555574 CIFC27 H38 O3P -110.004; 10.563; 12.631
94.414; 111.883; 93.763
1228.5Shen, Yangyong; Qi, Jifeng; Mao, Zhenjun; Cui, Sunliang
Fe-Catalyzed Hydroalkylation of Olefins with para-Quinone Methides.
Organic letters, 2016, 18, 2722-2725
1555575 CIFC16 H15 F3 N2P 21 21 216.37164; 8.13751; 26.6535
90; 90; 90
1381.96Ma, Wenpeng; Chen, Fei; Liu, Youran; He, Yan-Mei; Fan, Qing-Hua
Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives.
Organic letters, 2016, 18, 2730-2733
1555576 CIFC27 H24 N2 O2 SP 1 21 110.581; 9.532; 11.106
90; 90.577; 90
1120.1Ma, Wenpeng; Chen, Fei; Liu, Youran; He, Yan-Mei; Fan, Qing-Hua
Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives.
Organic letters, 2016, 18, 2730-2733
1555577 CIFC18 H17 N O3P -19.2442; 9.4365; 10.1285
109.029; 92.163; 110.061
773.37Li, Chao; Jiang, Kun; Ouyang, Qin; Liu, Tian-Yu; Chen, Ying-Chun
[3 + 1]- and [3 + 2]-Cycloadditions of Azaoxyallyl Cations and Sulfur Ylides.
Organic letters, 2016, 18, 2738-2741
1555578 CIFC24 H19 N0.25 O3P c a 2120.6513; 5.9284; 14.7885
90; 90; 90
1810.5Li, Chao; Jiang, Kun; Ouyang, Qin; Liu, Tian-Yu; Chen, Ying-Chun
[3 + 1]- and [3 + 2]-Cycloadditions of Azaoxyallyl Cations and Sulfur Ylides.
Organic letters, 2016, 18, 2738-2741
1555579 CIFC49 H42 B Cl3 F2 N2 O4P -111.661; 12.035; 17.572
102.313; 101.456; 102.201
2276.9Gobo, Yuki; Yamamura, Masaki; Nakamura, Takashi; Nabeshima, Tatsuya
Synthesis and Chiroptical Properties of a Ring-Fused BODIPY with a Skewed Chiral π Skeleton.
Organic letters, 2016, 18, 2719-2721
1555580 CIFC48 H41 B F2 N2 O4C 1 2/c 119.489; 25.41; 16.809
90; 100.702; 90
8179Gobo, Yuki; Yamamura, Masaki; Nakamura, Takashi; Nabeshima, Tatsuya
Synthesis and Chiroptical Properties of a Ring-Fused BODIPY with a Skewed Chiral π Skeleton.
Organic letters, 2016, 18, 2719-2721
1555581 CIFC21 H33 N O2 SiP 1 21/n 116.5088; 8.4395; 16.9774
90; 109.4; 90
2231.1Boobalan, Ramadoss; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Ruthenium-Catalyzed C-H Alkynylation of Aromatic Amides with Hypervalent Iodine-Alkyne Reagents.
Organic letters, 2016, 18, 3314-3317
1555582 CIFC19 H28 Cl N O2 SiP 1 21/c 118.781; 13.854; 8.134
90; 93.886; 90
2111.5Boobalan, Ramadoss; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Ruthenium-Catalyzed C-H Alkynylation of Aromatic Amides with Hypervalent Iodine-Alkyne Reagents.
Organic letters, 2016, 18, 3314-3317
1555583 CIFC43 H47 N3 O5P 1 21 18.9792; 16.193; 13.2363
90; 106.625; 90
1844.1Gorske, Benjamin C.; Mumford, Emily M.; Conry, Rebecca R.
Tandem Incorporation of Enantiomeric Residues Engenders Discrete Peptoid Structures.
Organic letters, 2016, 18, 2780-2783
1555584 CIFC49 H55 N3 O6P 1 21 112.9668; 13.1573; 13.5181
90; 109.297; 90
2176.7Gorske, Benjamin C.; Mumford, Emily M.; Conry, Rebecca R.
Tandem Incorporation of Enantiomeric Residues Engenders Discrete Peptoid Structures.
Organic letters, 2016, 18, 2780-2783
1555585 CIFC15 H23 N O2 SP 21 21 216.5067; 10.2546; 22.3875
90; 90; 90
1493.77Kubiak, 2nd, Robert W; Mighion, Jeffrey D.; Wilkerson-Hill, Sidney M; Alford, Joshua S.; Yoshidomi, Tetsushi; Davies, Huw M. L.
Enantioselective Intermolecular C-H Functionalization of Allylic and Benzylic sp(3) C-H Bonds Using N-Sulfonyl-1,2,3-triazoles.
Organic letters, 2016, 18, 3118-3121
1555586 CIFC26 H26 Br N O5P -19.8599; 11.9104; 11.9139
61.836; 72.739; 86.003
1173.79Das, Saikat; Chakrabarty, Shyamal; Daniliuc, Constantin G.; Studer, Armido
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor-Acceptor Cyclopropanes with Nitrosoarenes.
Organic letters, 2016, 18, 2784-2787
1555587 CIFC22 H24 Br N O5P 21 21 218.662; 9.2342; 26.0487
90; 90; 90
2083.55Das, Saikat; Chakrabarty, Shyamal; Daniliuc, Constantin G.; Studer, Armido
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor-Acceptor Cyclopropanes with Nitrosoarenes.
Organic letters, 2016, 18, 2784-2787
1555588 CIFC53.59 H49.59 Cl1.77 Cu N6 O2P -18.0804; 16.5626; 17.4337
82.85; 78.821; 77.371
2225.3Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555589 CIFC54 H52 Cl3 Cu N6P 1 21/c 112.031; 30.509; 13.9111
90; 113.596; 90
4679.2Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555590 CIFC55.5 H50.5 Cl4.5 Cu N6C 1 2/c 125.4929; 11.6131; 33.0447
90; 98.807; 90
9667.6Berionni Berna, Beatrice; Nardis, Sara; Galloni, Pierluca; Savoldelli, Andrea; Stefanelli, Manuela; Fronczek, Frank R.; Smith, Kevin M.; Paolesse, Roberto
β-Pyrrolopyrazino Annulated Corroles via a Pictet-Spengler Approach.
Organic letters, 2016, 18, 3318-3321
1555591 CIFC45 H52 Cl2 O12 P2P 1 21 113.3931; 9.5262; 17.8614
90; 101.589; 90
2232.4Durantie, Estelle; Huwiler, Samuel; Leroux, Jean-Christophe; Castagner, Bastien
A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates.
Organic letters, 2016, 18, 3162-3165
1555592 CIFC66 H66 O12 P2P 111.2057; 15.2204; 18.506
71.165; 81.596; 89.993
2951.5Durantie, Estelle; Huwiler, Samuel; Leroux, Jean-Christophe; Castagner, Bastien
A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates.
Organic letters, 2016, 18, 3162-3165
1555593 CIFC27 H36 F3 N O3 S2 SiP -17.1867; 11.58; 17.91
87.008; 85.211; 87.346
1482Karmakar, Rajdip; Mamidipalli, Phani; Salzman, Ryan M.; Hong, Seongwon; Yun, Sang Young; Guo, Wei; Xia, Yuanzhi; Lee, Daesung
Benzannulation of Triynes Initiated by an Alder-Ene Reaction and Subsequent Trifluoromethylthiolate Addition.
Organic letters, 2016, 18, 3530-3533
1555594 CIFC27 H21 N OP 1 21 110.7656; 8.6732; 11.0548
90; 95.097; 90
1028.13Cioc, Răzvan C; Schuckman, Peter; Preschel, Hans D.; Vlaar, Tjøstil; Ruijter, Eelco; Orru, Romano V. A.
Brønsted Acid-Catalyzed Cyanotritylation of Aldehydes by Trityl Isocyanide.
Organic letters, 2016, 18, 3562-3565
1555595 CIFC24 H21 Cl F3 N O4C 1 2/c 126.236; 8.1806; 21.79
90; 100.102; 90
4604.2Zhu, Yuanyuan; Dong, Zhenghao; Cheng, Xin; Zhong, Xiaoling; Liu, Xiaolin; Lin, Li; Shen, Zhiqiang; Yang, Peiju; Li, Yuan; Wang, Hailin; Yan, Wenjin; Wang, Kairong; Wang, Rui
Asymmetric Synthesis of CF3- and Indole-Containing Thiochromanes via a Squaramide-Catalyzed Michael-Aldol Reaction.
Organic letters, 2016, 18, 3546-3549
1555596 CIFC31 H27 Cl F3 N O5 SP 1 21 110.4656; 10.4575; 26.8799
90; 89.999; 90
2941.84Zhu, Yuanyuan; Dong, Zhenghao; Cheng, Xin; Zhong, Xiaoling; Liu, Xiaolin; Lin, Li; Shen, Zhiqiang; Yang, Peiju; Li, Yuan; Wang, Hailin; Yan, Wenjin; Wang, Kairong; Wang, Rui
Asymmetric Synthesis of CF3- and Indole-Containing Thiochromanes via a Squaramide-Catalyzed Michael-Aldol Reaction.
Organic letters, 2016, 18, 3546-3549
1555597 CIFC30 H38 O5P 1 21/n 123.324; 9.264; 26.981
90; 105.014; 90
5631Yuan, Zhenbo; Wei, Weiwei; Lin, Aijun; Yao, Hequan
Bifunctional Organo/Metal Cooperatively Catalyzed [3 + 2] Annulation of para-Quinone Methides with Vinylcyclopropanes: Approach to Spiro[4.5]deca-6,9-diene-8-ones.
Organic letters, 2016, 18, 3370-3373
1555598 CIFC19 H20 N2 O1.76R 3 :H24.3768; 24.3768; 7.2197
90; 90; 120
3715.4Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555599 CIFC19 H20 N2 OP 21 21 216.8328; 11.6515; 19.2975
90; 90; 90
1536.32Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555600 CIFC19 H21 I N2 OP 1 21 17.272; 9.1963; 13.4788
90; 101.735; 90
882.6Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177
1555601 CIFC19 H20 N2 OP 1 21 110.3077; 7.8255; 10.6948
90; 117.859; 90
762.69Rahman, M. Toufiqur; Deschamps, Jeffrey R.; Imler, Gregory H.; Schwabacher, Alan W.; Cook, James M.
Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide.
Organic letters, 2016, 18, 4174-4177

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