Crystallography Open Database

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1518403 CIFC25 H17 N OP -18.2167; 16.3939; 25.795
90; 86.989; 90		3469.9Wang, Zhen; Li, Ting
Facile Synthesis of 6-Acylated Pyrido[2,1-a]isoindoles from 2-Arylpyridines and γ-Substituted tert-Propargyl Alcohols via Rhodium-Catalyzed C-H Bond Activation and β-Carbon Elimination.
Organic letters, 2015, 17, 1348
1518421 CIFC23 H28 N2 O4 SP 1 21/n 110.543; 9.344; 22.465
90; 92.128; 90		2211.6Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518422 CIFC23 H28 N2 O4 SP n a 2126.688; 18.145; 9.062
90; 90; 90		4388.3Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518427 CIFC15 H9 F3 N2 O2P 1 21/n 116.6085; 7.853; 20.7239
90; 103.721; 90		2625.8Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518428 CIFC15 H11 Cl N2 O2C 1 2/c 119.16; 11.3942; 15.345
90; 126.612; 90		2689Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518455 CIFC29 H37 N3 O4P 21 21 217.788; 16.0615; 20.7023
90; 90; 90		2589.6Lee, Pin-Sheng; Yoshikai, Naohiko
Cobalt-catalyzed enantioselective directed C-h alkylation of indole with styrenes.
Organic letters, 2015, 17, 22-25
1518456 CIFC21 H28 O4 SC 1 2 119.3925; 6.0017; 17.9993
90; 107.635; 90		1996.45Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518457 CIFC21 H28 O4P 21 21 216.2688; 16.308; 18.2849
90; 90; 90		1869.29Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518458 CIFC24 H25 N O5P 21 21 219.0419; 12.2803; 19.0748
90; 90; 90		2118.01Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518459 CIFC24 H23 N O4P 1 21/c 19.6257; 24.6776; 9.1983
90; 108.936; 90		2066.71Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518460 CIFC25 H25 N O4P -110.1067; 11.5787; 19.2079
83.811; 82.159; 76.354		2157.2Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518461 CIFC24 H21 Cl2 N O4C 1 2 121.3083; 16.6395; 17.8923
90; 118.967; 90		5550.3Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518462 CIFC21 H21 Br N2 O3 SP c a 2124.0183; 11.2598; 7.4174
90; 90; 90		2005.97Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518463 CIFC21 H21 Br N2 O3 SP 1 21/n 18.12; 11.101; 21.7055
90; 94.955; 90		1949.2Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518464 CIFC19 H26 O7P 21 21 219.1452; 12.5627; 16.2841
90; 90; 90		1870.85Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518465 CIFC19 H26 O7P 329.2683; 9.2683; 18.5901
90; 90; 120		1382.97Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518466 CIFC24.5 H26.52 O7C 1 2 143.491; 5.5109; 18.3225
90; 95.331; 90		4372.4McDonald, Benjamin R.; Nibbs, Antoinette E.; Scheidt, Karl A.
A biomimetic strategy to access the silybins: total synthesis of (-)-isosilybin a.
Organic letters, 2015, 17, 98-101
1518467 CIFC18 H26 O4P -17.1391; 7.5445; 15.455
88.709; 83.268; 76.661		804.4Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518468 CIFC19 H24 O7 SP 1 21/n 116.194; 6.597; 18.175
90; 102.603; 90		1894.9Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518482 CIFC24 H20 N2 OP b c a8.8127; 13.2298; 32.5
90; 90; 90		3789.2Fan, Zhoulong; Song, Shanshan; Li, Wei; Geng, Kaijun; Xu, Youjun; Miao, Ze-Hong; Zhang, Ao
Rh(III)-Catalyzed Redox-Neutral C-H Activation of Pyrazolones: An Economical Approach for the Synthesis of N-Substituted Indoles.
Organic letters, 2015, 17, 310-313
1518483 CIFC23 H24 Cl N O4P -110.0098; 10.1777; 12.0505
67.347; 70.617; 79.738		1066.95Craig, Alexander J.; van der Salm, Louise; Stevens-Cullinane, Lars; Lucas, Nigel T.; Tan, Eng Wui; Hawkins, Bill C.
Expedient Metal-Free Synthesis of 1,3-Oxazinen-4-ones.
Organic letters, 2015, 17, 234-237
1518484 CIFC54 H75 N8 O16 SP 19.1948; 12.5947; 13.668
79.379; 77.83; 78.547		1499.6Ganesh Kumar, Mothukuri; Mali, Sachitanand M.; Raja, K. Muruga Poopathi; Gopi, Hosahudya N.
Design of Stable β-Hairpin Mimetics through Backbone Disulfide Bonds.
Organic letters, 2015, 17, 230-233
1518485 CIFC22 H16 I N O2 SP 1 21/c 18.0428; 19.587; 12.8121
90; 104.921; 90		1950.29Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518486 CIFC21 H14 I N O2 SP -18.195; 10.1773; 11.9407
86.942; 83.912; 76.661		963.13Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518487 CIFC24 H24 O6C 1 c 117.142; 9.0363; 12.653
90; 90.03; 90		1960Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518488 CIFC16 H16 O5P n a 2114.969; 7.307; 12.761
90; 90; 90		1395.8Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518489 CIFC22 H14 Co2 O11P -18.0572; 8.3258; 17.63
88.79; 84.64; 75.45		1139.7Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518490 CIFC36 H34 Co2 F6 N O5 P2P 21 21 215.8829; 19.5684; 11.5831
90; 90; 90		3600.1Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518491 CIFC30 H37 Co2 N3 O5 P2 SiP 1 21 18.8649; 20.8055; 9.1083
90; 101.487; 90		1646.3Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518492 CIFC32 H22 B Cl3 F4 N2 O2C 1 2/c 130.8526; 11.997; 18.7562
90; 113.744; 90		6354.75Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518493 CIFC15 H10 Cl N O3P 1 21/n 18.5347; 14.9824; 10.2813
90; 96.632; 90		1305.88Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518494 CIFC18 H20 N2 O2 SP c a 2112.7796; 13.8018; 18.4448
90; 90; 90		3253.32Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518495 CIFC16 H12 Br N3P 3210.18; 10.18; 10.954
90; 90; 120		983.1Tang, Hai-Tao; Xiong, Kai; Li, Ren-Hao; Ding, Zong-Cang; Zhan, Zhuang-Ping
Synthesis of 5,6-Dihydropyrazolo[1,5-c]quinazolines through Gold-Catalyzed Chemoselective Bicyclization of N-Propargylic Sulfonylhydrazones.
Organic letters, 2015, 17, 326-329
1518565 CIFC24 H23 N O3P -112.483; 12.4917; 14.6608
71.195; 68.259; 69.138		1935.93Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518566 CIFC24 H27 N O3P 1 21/n 113.1285; 8.9817; 17.2111
90; 107.754; 90		1932.8Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518567 CIFC24 H22 Br N O3P 21 21 218.9945; 12.4644; 17.7143
90; 90; 90		1985.97Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518568 CIFC31 H37 N5 O8 SP 1 21 110.9519; 18.6953; 14.864
90; 100.907; 90		2988.4Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518569 CIFC15 H19 N O2P -16.6977; 8.9166; 11.8671
97.4234; 102.013; 108.163		644.13Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518570 CIFC13 H15 N O2P 21 21 219.0807; 9.5935; 12.844
90; 90; 90		1118.91Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518571 CIFC8 H13 N O3P -17.0255; 8.3274; 8.5054
64.8193; 75.8585; 86.3999		436.19Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518572 CIFC18 H17 N O2C 1 2/c 116.694; 9.6688; 18.2592
90; 101.972; 90		2883.1Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518573 CIFC25 H20 N2 O4P 1 21/c 110.359; 8.616; 22.998
90; 98.931; 90		2027.8Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518574 CIFC26 H22 N2 O4P -18.5149; 11.4869; 11.4981
90.53; 111.599; 91.352		1045.17Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518575 CIFC26 H22 N2 O4P 1 21/c 18.1999; 23.636; 10.7112
90; 97.847; 90		2056.5Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518576 CIFC25 H21 N5 O4P n a 2115.0058; 16.0652; 9.235
90; 90; 90		2226.29Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518577 CIFC26 H21 N3 O4 SP 1 21/n 113.7112; 7.9341; 22.1644
90; 101.626; 90		2361.71Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518578 CIFC25 H22 N2 O5P 1 21/n 112.2086; 8.2983; 20.1576
90; 94.952; 90		2034.56Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518579 CIFC25 H19 N3 O4I 41/a :225.4401; 25.4401; 14.9071
90; 90; 90		9647.9Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518580 CIFC25 H19 N3 O4P -18.2122; 14.1107; 17.9598
100.563; 95.565; 90.101		2035.86Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518581 CIFC14 H16 F N O3P 1 21 110.68; 10.806; 12.352
90; 107.01; 90		1363.2Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518582 CIFC17 H14 F N O3P 1 21 16.5754; 10.311; 11.071
90; 95.19; 90		747.5Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518583 CIFC14 H18 O2P 21 21 218.0591; 9.6081; 15.5767
90; 90; 90		1206.14Homs, Anna; Muratore, Michael E.; Echavarren, Antonio M.
Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization.
Organic letters, 2015, 17, 461-463
1518584 CIFC32 H33 Br N O2 PP 1 21/n 18.4438; 10.9189; 32.745
90; 95.201; 90		3006.6Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518585 CIFC33 H35 Au Br Cl3 N O2 PP 1 21/n 19.848; 24.3169; 15.0477
90; 104.667; 90		3486.1Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518586 CIFC60.5 H56 N4 O6C 1 c 116.1723; 24.7158; 24.1251
90; 90.474; 90		9642.7Liu, Lei; Carroll, Patrick J.; Kozlowski, Marisa C.
Vanadium-catalyzed regioselective oxidative coupling of 2-hydroxycarbazoles.
Organic letters, 2015, 17, 508-511
1518613 CIFC22 H17 N OP 1 21/n 18.8912; 16.859; 11.238
90; 108.555; 90		1597Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518614 CIFC22 H16 F N OP 1 21/n 18.922; 16.7585; 11.2263
90; 108.038; 90		1596.05Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518615 CIFC52 H50 N4 Ni O2P 1 21/c 118.2078; 16.5273; 14.8317
90; 98.447; 90		4414.8Gehrold, Andreas C.; Bruhn, Torsten; Schneider, Heidi; Radius, Udo; Bringmann, Gerhard
Chiral and achiral basket-handle porphyrins: short synthesis and stereostructures of these versatile building blocks.
Organic letters, 2015, 17, 210-213
1518616 CIFC15 H13 N3C 1 2/c 117.719; 6.475; 22.501
90; 100.868; 90		2535.2Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
Correction to p-Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN3 for Synthesis of 4-Aryl-NH-1,2,3-triazoles.
Organic letters, 2015, 17, 393
1518617 CIFC37 H36 Cl2 N4 O8 S2P 21 21 2112.9116; 15.1292; 18.7417
90; 90; 90		3661Liang, Kangjiang; Deng, Xu; Tong, Xiaogang; Li, Dashan; Ding, Ming; Zhou, Ankun; Xia, Chengfeng
Copper-Mediated Dimerization to Access 3a,3a'-Bispyrrolidinoindoline: Diastereoselective Synthesis of (+)-WIN 64821 and (-)-Ditryptophenaline.
Organic letters, 2015, 17, 206-209
1518618 CIFC20 H17 Br N2 OP 19.8359; 10.161; 10.307
76.557; 73.136; 64.754		884.6Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518619 CIFC24 H20 N2 OP 21 21 2110.5861; 10.618; 17.0439
90; 90; 90		1915.79Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518620 CIFC16 H10 B F2 N3P 1 21/n 19.559; 9.3155; 15.051
90; 102.64; 90		1307.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518621 CIFC16 H9 B Cl F2 N3P 1 21/n 17.7337; 19.0699; 9.655
90; 105.059; 90		1375Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518622 CIFC15 H10 B F2 N3 SP 1 21/c 17.9215; 14.0077; 25.071
90; 102.609; 90		2714.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518623 CIFC22 H18 B F2 N3 SP -110.092; 10.383; 10.434
65.025; 82.642; 75.499		959.2Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518624 CIFC18 H10 B F2 N3P -17.4838; 9.1552; 11.5629
79.781; 71.778; 67.825		695.26Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518625 CIFC18 H9 B Br F2 N3P -19.1788; 9.5551; 9.9844
87.602; 71.441; 65.179		749.15Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518626 CIFC24 H17 B Br F2 N3 SC 1 2/c 111.3331; 34.017; 12.736
90; 109.159; 90		4638Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518627 CIFC21 H20 Cl N O3P 1 21/c 115.6314; 21.884; 11.7948
90; 108.565; 90		3824.8Li, Lei; Zhao, Yu-Long; Wang, Qian; Lin, Tao; Liu, Qun
Base-Promoted Oxidative C-H Functionalization of α-Amino Carbonyl Compounds under Mild Metal-Free Conditions: Using Molecular Oxygen as the Oxidant.
Organic letters, 2015, 17, 370-373
1518633 CIFC24 H17 N OP 1 21/n 19.5489; 9.6991; 19.1473
90; 97.465; 90		1758.31Li, Ziyuan; Huang, Xiaoqiang; Chen, Feng; Zhang, Chun; Wang, Xiaoyang; Jiao, Ning
Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors.
Organic letters, 2015, 17, 584-587
1518634 CIFC20 H22 B F3 K N OP 21 21 216.3906; 7.7434; 38.9797
90; 90; 90		1928.91Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518635 CIFC26 H29 B F4 N2 O2P 21 21 218.447; 16.3195; 17.2927
90; 90; 90		2383.8Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518636 CIFC46 H44 B3 N3 O7P 1 21/c 116.559; 16.774; 15.989
90; 115.658; 90		4003.2Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518637 CIFC27 H24 B3 N3 O12R -3 :H19.9798; 19.9798; 12.6217
90; 90; 120		4363.46Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518638 CIFC37 H33 B3 Cl3 N3 O7P 1 21/c 113.0661; 12.1247; 22.3242
90; 98.251; 90		3500Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518639 CIFC33 H40 B N O4 SiP 1 21/c 113.3949; 14.3478; 15.283
90; 92.281; 90		2934.9Kubota, Koji; Iwamoto, Hiroaki; Yamamoto, Eiji; Ito, Hajime
Silicon-tethered strategy for copper(i)-catalyzed stereo- and regioselective alkylboration of alkynes.
Organic letters, 2015, 17, 620-623
1518640 CIFC20 H22 N2 O5P -19.272; 15.087; 26.669
75.828; 88.836; 88.885		3616Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518641 CIFC18 H18 N2 O3P 1 21/n 18.2569; 11.5402; 15.727
90; 102.251; 90		1464.4Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518642 CIFC13 H12 O3P -19.562; 10.2591; 10.618
87.713; 85.512; 88.206		1037.16Kratochvíl, Jiří; Novák, Zdeněk; Ghavre, Mukund; Nováková, Lucie; Růžička, Aleš; Kuneš, Jiří; Pour, Milan
Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita-Stille Coupling of Iodoacrylates.
Organic letters, 2015, 17, 520-523
1518643 CIFC21 H18 N2 OP 21 21 218.964; 12.046; 16.315
90; 90; 90		1761.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518644 CIFC23 H20 N2 OP -16.345; 11.725; 13.3
67.812; 80.532; 84.005		902.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518645 CIFC24 H35 N3 O2P 1 21 112.8948; 9.7854; 18.3889
90; 94.667; 90		2312.6Li, Xun; Taechalertpaisarn, Jaru; Xin, Dongyue; Burgess, Kevin
Protein-Protein Interface Mimicry by an Oxazoline Piperidine-2,4-dione.
Organic letters, 2015, 17, 632-635
1518646 CIFC34 H56 N2 O7 Si2P 21 21 219.052; 19.871; 22.2031
90; 90; 90		3993.72Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518647 CIFC33 H44 N2 O7 SiP 1 21 118.0919; 10.7097; 18.935
90; 107.979; 90		3489.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518648 CIFC22 H28 N2 O7P 21 21 2111.0538; 12.5835; 15.8359
90; 90; 90		2202.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518649 CIFC17 H17 N O3P 1 21/c 18.9854; 18.5028; 9.4678
90; 109.249; 90		1486.07Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518650 CIFC25 H22 Cl N O4P -18.5929; 9.9207; 13.6227
73.585; 78.745; 86.593		1092.53Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518651 CIFC31 H27 N3 O2P 1 21 17.6192; 12.0803; 14.0233
90; 102.158; 90		1261.8Pertejo, Pablo; Corres, Nazaret; Torroba, Tomás; García-Valverde, María
Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones.
Organic letters, 2015, 17, 612-615
1518652 CIFC30 H38 N2 O7P 1 21 111.3323; 8.5548; 14.1288
90; 92.453; 90		1368.47Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518653 CIFC32 H40 N2 O7P 1 21 113.4499; 7.46; 14.9726
90; 104.948; 90		1451.46Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518654 CIFC42 H59 F3 O10P 1 21 113.4566; 8.18811; 19.1862
90; 100.629; 90		2077.74Inahashi, Yuki; Iwatsuki, Masato; Ishiyama, Aki; Matsumoto, Atsuko; Hirose, Tomoyasu; Oshita, Jun; Sunazuka, Toshiaki; Panbangred, Watanalai; Takahashi, Yoko; Kaiser, Marcel; Otoguro, Kazuhiko; O̅mura, Satoshi
Actinoallolides A-E, New Anti-trypanosomal Macrolides, Produced by an Endophytic Actinomycete, Actinoallomurus fulvus MK10-036.
Organic letters, 2015, 17, 864-867
1518655 CIFC13 H10 N2 O2 SP 1 21/c 111.9124; 7.5041; 14.67
90; 111.533; 90		1219.9Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518656 CIFC13 H10 N4 OP -16.9373; 8.2261; 9.7516
85.814; 78.171; 89.197		543.22Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518657 CIFC14 H11 N5P -17.9667; 8.6666; 9.6847
109.198; 107.554; 92.006		595.36Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518658 CIFC16 H19 N O4P 1 21 18.2102; 6.2167; 14.102
90; 90.69; 90		719.7Lou, Yan-Peng; Zheng, Chang-Wu; Pan, Ren-Ming; Jin, Qiao-Wen; Zhao, Gang; Li, Zhong
Enantioselective Direct Mannich Reactions of Cyclic β-Ketoesters Catalyzed by Chiral Phosphine via a Novel Dual-Reagent Catalysis.
Organic letters, 2015, 17, 688-691
1518659 CIFC25 H23 Br O S2 SeP 1 21/c 19.5704; 11.7332; 21.056
90; 97.692; 90		2343.1Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518660 CIFC20 H21 F O2 S2P 1 21/c 110.5963; 16.7072; 10.9555
90; 95.184; 90		1931.57Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518685 CIFC52 H48 N4 O4P n a 2118.809; 10.08; 20.725
90; 90; 90		3929Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518686 CIFC62 H66 Cl6 N4 O12P -19.8315; 14.743; 21.249
101.193; 91.334; 94.028		3011.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518687 CIFC63 H70 N4 O16P -111.12; 14.029; 20.02
108.726; 98.537; 94.981		2894.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518712 CIFC21 H28 O3P 21 21 216.0078; 15.1366; 20.0221
90; 90; 90		1820.76Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518713 CIFC23 H27 F3 O3P 21 21 216.2097; 14.9142; 23.193
90; 90; 90		2147.97Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518718 CIFC18 H26 O4 SiP b c a16.759; 7.4334; 30.141
90; 90; 90		3754.9Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518719 CIFC18 H26 O4 SiP -16.1239; 16.8945; 17.8873
91.468; 95.3024; 90.184		1842.1Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518723 CIFC32 H28 O4 SiP -17.0418; 10.4998; 17.4226
93.591; 96.204; 103.663		1239.21Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518724 CIFC31 H28 O4 SiP 1 21/n 114.0146; 10.5314; 16.6752
90; 100.775; 90		2417.8Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518725 CIFC18 H12 F N O3P 1 21/c 13.798; 11.416; 31.2
90; 90.82; 90		1353Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518726 CIFC22 H16 F4 O3P -17.668; 11.45; 11.497
97.96; 98.584; 103.944		952.6Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518747 CIFC14 H9 Cl N4 O2P -111.31; 13.792; 13.982
93.902; 90.56; 112.233		2012.7Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518748 CIFC15 H11 Br N4 O2P b c a10.784; 9.6655; 28.858
90; 90; 90		3007.9Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518770 CIFC20 H16 Cl4 N2P b c a11.2813; 14.1148; 24.5832
90; 90; 90		3914.5Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518771 CIFC18 H26 Cl2 N2P -19.3474; 9.8657; 12.3923
66.695; 69.579; 62.115		908.59Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518772 CIFC28 H23 Br Cl3 N O2P 21 21 219.6557; 10.7366; 25.0366
90; 90; 90		2595.53Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518773 CIFC26 H21 N O2 SP 21 21 217.3516; 9.5635; 29.4896
90; 90; 90		2073.33Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518783 CIFC23 H16 N2P 1 21/c 114.9264; 8.5389; 13.3223
90; 96.518; 90		1687.02Zhang, Wei; Wei, Jun; Fu, Shaomin; Lin, Dongen; Jiang, Huanfeng; Zeng, Wei
Highly Stereoselective Ruthenium(II)-Catalyzed Direct C2-syn-Alkenylation of Indoles with Alkynes.
Organic letters, 2015, 17, 1349-1352
1518820 CIFC23 H17 N OP 19.9575; 10.7208; 16.4862
91.531; 105.749; 104.208		1633.82Yang, Xiao-Fei; Hu, Xu-Hong; Loh, Teck-Peng
Expedient Synthesis of Pyrroloquinolinones by Rh-Catalyzed Annulation of N-Carbamoyl Indolines with Alkynes through a Directed C-H Functionalization/C-N Cleavage Sequence.
Organic letters, 2015, 17, 1481-1484
1518842 CIFC15 H13 F O2 SP 21 21 215.9536; 7.269; 31.978
90; 90; 90		1383.9Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518936 CIFC18 H24 F N O4 SP 1 21/c 19.8882; 17.552; 11.4151
90; 103.067; 90		1929.9Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518937 CIFC13 H15 N O4 SP -16.7205; 8.781; 11.3856
103.22; 104.242; 92.033		630.98Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518938 CIFC19 H28 N2 O4 SP -110.0063; 10.3287; 10.8385
65.843; 70.701; 84.706		963.4Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518939 CIFC15 H18 N2 SP 1 21/c 110.8363; 14.406; 9.9733
90; 117.4; 90		1382.2Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518940 CIFC15 H21 N O3 SP 1 21/c 17.3226; 10.563; 18.9019
90; 92.929; 90		1460.13Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518941 CIFC14 H19 N O3 SP b c a8.4818; 10.9461; 30.035
90; 90; 90		2788.5Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.
Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.
Organic letters, 2015, 17, 1922-1925
1518989 CIFC19 H12 Cl2 N2P 1 21/c 112.7382; 11.0562; 12.4976
90; 112.701; 90		1623.76Tiwari, Virendra Kumar; Kamal, Neha; Kapur, Manmohan
Ruthenium-catalyzed heteroatom-directed regioselective C-h arylation of indoles using a removable tether.
Organic letters, 2015, 17, 1766-1769
1518990 CIFC17 H17 O P SiP c a 2114.4427; 6.5207; 16.6673
90; 90; 90		1569.67Xu, Youzhi; Wang, Zhihua; Gan, Zhenjie; Xi, Qiuzhen; Duan, Zheng; Mathey, François
Versatile synthesis of phospholides from open-chain precursors. Application to annelated pyrrole- and silole-phosphole rings.
Organic letters, 2015, 17, 1732-1734
1518991 CIFC21 H17 F O2 SP 1 21/n 112.402; 5.782; 24.377
90; 100.253; 90		1720.1Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518992 CIFC16 H16 O2 SP 21 21 215.7471; 8.0541; 31.351
90; 90; 90		1451.2Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518993 CIFC21 H18 O2 SP 1 21/n 112.3084; 5.8277; 24.345
90; 100.373; 90		1717.7Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang
Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.
Organic letters, 2015, 17, 1692-1695
1518994 CIFC14 H17 N O3 SC 1 2/c 125.7457; 5.8011; 19.0494
90; 98.23; 90		2815.79Cheng, Cungui; Liu, Shuiyou; Zhu, Gangguo
Palladium-catalyzed cycloisomerization and aerobic oxidative cycloisomerization of homoallenyl amides: a facile and divergent approach to 2-aminofurans.
Organic letters, 2015, 17, 1581-1584
1518995 CIFC15 H21 N O4 SP b c n16.428; 13.329; 14.387
90; 90; 90		3150Zhu, Haitao; Chen, Pinhong; Liu, Guosheng
Palladium-catalyzed intramolecular aminoacetoxylation of unactivated alkenes with hydrogen peroxide as oxidant.
Organic letters, 2015, 17, 1485-1488
1518996 CIFC20 H20 N2 O3P 21 21 219.8991; 10.1513; 17.5003
90; 90; 90		1758.6Yetra, Santhivardhana Reddy; Mondal, Santigopal; Suresh, Eringathodi; Biju, Akkattu T.
Enantioselective Synthesis of Functionalized Pyrazoles by NHC-Catalyzed Reaction of Pyrazolones with α,β-Unsaturated Aldehydes.
Organic letters, 2015, 17, 1417-1420
1518997 CIFC11 H14 O3P n a 2114.5121; 5.9558; 24.1332
90; 90; 90		2085.9Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei
Bioinspired Organocatalytic Aerobic C-H Oxidation of Amines with an ortho-Quinone Catalyst.
Organic letters, 2015, 17, 1469-1472
1518998 CIFC16 H14 O2P 21 21 218.477; 8.5847; 17.547
90; 90; 90		1276.94Jiang, Liyin; Jia, Tao; Wang, Min; Liao, Jian; Cao, Peng
Pd-catalyzed enantioselective hydroalkoxylation of alkoxyallenes with phenol for construction of acyclic o,o-acetals.
Organic letters, 2015, 17, 1070-1073
1518999 CIFC17 H13 F O3 SP 1 21/n 19.2698; 11.0134; 15.0573
90; 105.111; 90		1484.08Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Bi(OTf)3-Mediated Cycloisomerization of γ-Alkynyl Arylketones: Application to the Synthesis of Substituted Furans.
Organic letters, 2015, 17, 1264-1267
1519496 CIFC22 H20 Br NP 16.134; 7.123; 10.777
102.328; 106.299; 90.659		440.2Zhang, Zhenhua; Du, Haifeng
Cis-selective and highly enantioselective hydrogenation of 2,3,4-trisubstituted quinolines.
Organic letters, 2015, 17, 2816-2819
1519622 CIFC22 H18 Cl N O3 PdP 1 21/c 119.306; 4.5687; 22.128
90; 103.674; 90		1896.4Ren, Zhi; Schulz, Jonathan E.; Dong, Guangbin
Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode.
Organic letters, 2015, 17, 2696-2699
1519623 CIFC15 H10 I N O2C 1 c 124.877; 7.087; 7.92
90; 90.593; 90		1396.2Huang, Hai; Zhu, Xiaolin; He, Guangke; Liu, Qi; Fan, Junzhen; Zhu, Hongjun
Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides.
Organic letters, 2015, 17, 2510-2513
1519625 CIFC32 H30 B NP 1 21/c 110.2671; 10.1236; 23.3329
90; 98.876; 90		2396.18Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519626 CIFC32 H32 B NP 1 21/c 110.0993; 10.2609; 23.8794
90; 97.3582; 90		2454.19Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519627 CIFC38 H34 B NP -18.8087; 11.1753; 16.1219
72.148; 78.052; 74.662		1443.04Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519628 CIFC102 H70 B4 O20C 1 2/c 130.624; 56.38; 22.177
90; 93.399; 90		38223Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1519629 CIFC21 H26 N2 O2 SP 1 21/c 17.3915; 13.779; 19.135
90; 93.863; 90		1944.4Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519630 CIFC16 H14 N2 O2 SP 1 21/c 111.225; 13.361; 11.0143
90; 118.102; 90		1457.2Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519631 CIFC17 H16 N2 O2 SP 1 21/c 18.9148; 16.7339; 10.5655
90; 95.855; 90		1567.93Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519651 CIFC14 H15 F3 O4 SP 1 21/n 15.4571; 34.89; 7.6271
90; 96.378; 90		1443.2Liu, Yafei; Shao, Xinxin; Zhang, Panpan; Lu, Long; Shen, Qilong
Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether.
Organic letters, 2015, 17, 2752-2755
1519652 CIFC47 H59 N O5P n 21 a18.4589; 58.006; 11.59672
90; 90; 90		12416.9Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519653 CIFC41 H46 O5C 1 2/c 134.9361; 10.48642; 26.842
90; 135.583; 90		6882.4Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519654 CIFC48.5 H58 O6.5P 1 21 120.7243; 10.45113; 21.5504
90; 113.543; 90		4279.1Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519655 CIFC20 H16 Br N O4C 1 c 114.0307; 8.5721; 15.203
90; 109.89; 90		1719.4Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519656 CIFC25 H20 N2 O2P 1 21/c 113.373; 16.581; 8.8083
90; 93.638; 90		1949.2Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519657 CIFC24 H28 Cl N O7P 1 21/n 110.5446; 9.5462; 24.575
90; 91.778; 90		2472.5Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519658 CIFC28 H28 Br N O6P 21 21 2110.409; 15.4718; 16.588
90; 90; 90		2671.4Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519694 CIFC14 H11 N O4 SP 1 21/c 15.7372; 21.0648; 10.9631
90; 94.428; 90		1321Singh, Rahul; Allam, Bharat Kumar; Singh, Neetu; Kumari, Kumkum; Singh, Satish Kumar; Singh, Krishna Nand
A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones.
Organic letters, 2015, 17, 2656-2659
1519695 CIFC23 H22 O2P 21 21 218.099; 13.445; 16.407
90; 90; 90		1786.6Mitra, Nirmal K.; Meudom, Rolande; Gorden, John D.; Merner, Bradley L.
A non-cross-coupling approach to arene-bridged macrocycles: synthesis, structure, and direct, regioselective functionalization of a cycloparaphenylene fragment.
Organic letters, 2015, 17, 2700-2703
1519696 CIFC13 H13 F OP 21 21 216.1061; 18.8064; 27.8827
90; 90; 90		3201.88Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519697 CIFC9 H10 Br F OP 1 21 18.013; 5.1662; 10.972
90; 93.376; 90		453.4Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519698 CIFC10 H13 F OP 21 21 215.5342; 11.1421; 14.6505
90; 90; 90		903.39Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519755 CIFC15 H16 O4P 1 21/c 17.4665; 21.583; 8.4033
90; 107.586; 90		1290.9Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song
Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans.
Organic letters, 2015, 17, 2708-2711
1519756 CIFC30 H42 O5P 1 21 17.3312; 12.6193; 14.4778
90; 98.847; 90		1323.47Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun
Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis.
Organic letters, 2015, 17, 2760-2763
1519757 CIFC10 H7 Br Cl2 N2 OP b c a12.6226; 12.3709; 14.1124
90; 90; 90		2203.7Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519758 CIFC12 H12 Br2 N2 OP 1 21/c 17.3945; 20.124; 17.43
90; 91.44; 90		2592.9Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519759 CIFC11 H10 Br2 N2P 1 21/c 114.9133; 10.5056; 7.3297
90; 103.561; 90		1116.35Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519760 CIFC11 H7 Cl2 F3 N2 O1.5P 1 21/c 17.501; 40.025; 16.7795
90; 94.664; 90		5021Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519761 CIFC11 H9 Br2 F N2P b c a14.443; 7.5861; 21.306
90; 90; 90		2334.4Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519848 CIFC12 H14 O3P 1 21/c 18.8887; 18.4179; 6.9957
90; 115.638; 90		1032.52Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519849 CIFC12 H14 O3P 1 21/c 110.7308; 8.7467; 12.089
90; 109.485; 90		1069.68Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519850 CIFC22 H16 Br N O2P 1 21/c 15.7399; 15.532; 20.365
90; 96.93; 90		1802.3Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine.
Organic letters, 2015, 17, 2780-2783
1519851 CIFC16 H12 N4P 1 21/c 14.8624; 11.167; 23.437
90; 94.33; 90		1269Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles.
Organic letters, 2015, 17, 2820-2823
1519923 CIFC21 H34 O3P 1 21 16.1791; 23.0423; 6.9392
90; 110.037; 90		928.21Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R.
Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones.
Organic letters, 2015, 17, 2808-2811
1519924 CIFC25 H21 Fe N3P 1 21/c 110.9392; 8.3314; 22.5089
90; 102.759; 90		2000.78Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu
Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles.
Organic letters, 2015, 17, 2860-2863
1519998 CIFC20 H30 N0 O5P 21 21 217.0685; 15.143; 17.388
90; 90; 90		1861.2Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1519999 CIFC20 H28 O5P 1 21 19.4777; 7.3392; 13.4089
90; 91.432; 90		932.41Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1520000 CIFC29 H36 O8P 1 21/c 113.2416; 13.1779; 15.2428
90; 109.387; 90		2509Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis.
Organic letters, 2015, 17, 2574-2577
1520001 CIFC54 H46 Co N2 P3P 1 21/n 114.376; 14.699; 21.34
90; 107.79; 90		4293.8Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J.
Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts.
Organic letters, 2015, 17, 2716-2719
1520002 CIFC29 H38 O8P 1 21/n 19.3612; 19.6336; 14.1965
90; 101.762; 90		2554.4Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520003 CIF
Paper		C42 H50 O10P -19.6397; 13.6008; 15.0461
83.6966; 77.488; 77.9768		1879.2Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520004 CIFC30.25 H41 O8P -111.3343; 15.4666; 16.487
85.1124; 78.3773; 78.5231		2771.3Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520005 CIFC15 H21 N O2P 1 21/c 18.5353; 10.6984; 15.609
90; 104.429; 90		1380.4Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi
Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone.
Organic letters, 2015, 17, 2724-2727
1520068 CIFC32 H36 Br2 N4 O2P 1 21/c 110.037; 8.2451; 18.991
90; 101.279; 90		1541.3Zhu, Xiaxia; Du, Haifeng
A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines.
Organic letters, 2015, 17, 3106-3109
1520116 CIFC28 H19 NP -19.0455; 9.563; 11.529
103.716; 98.763; 98.986		938.1Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong
Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines.
Organic letters, 2015, 17, 2936-2939
1520117 CIFC17.5 H18 F8 I O3.5 S2P -18.9435; 12.1892; 12.2642
63.163; 87.526; 77.6		1162.92Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio
Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.
Organic letters, 2015, 17, 3038-3041
1520220 CIFC24 H19 NC 1 2/c 142.784; 6.0454; 31.552
90; 119.951; 90		7071Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520221 CIFC30 H23 NP 1 21/c 112.0216; 6.2012; 30.083
90; 101.315; 90		2199Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520222 CIFC23 H19 NC 1 2/c 129.558; 6.041; 19.696
90; 104.661; 90		3402.4Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520223 CIFC14 H16 Cl3 N O3P 3216.1172; 16.1172; 5.6393
90; 90; 120		1268.63Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars
Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation.
Organic letters, 2015, 17, 2902-2904
1520224 CIFC22 H22 N4 O2 SP 1 21 110.363; 9.318; 11.453
90; 112.7; 90		1020.3Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui
Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines.
Organic letters, 2015, 17, 3004-3007
1520225 CIFC13 H21 N3 O3P 1 21/c 14.5905; 23.474; 13.2529
90; 91.746; 90		1427.4Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen
Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water.
Organic letters, 2015, 17, 2980-2983
1520297 CIFC52 H60 Br N4 O18 S2C 1 2/c 126.6011; 19.037; 14.4208
90; 114.731; 90		6633Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520298 CIFC52 H86 N4 O32 S2P 1 21/n 111.8381; 23.4128; 11.8991
90; 107.339; 90		3148.12Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520299 CIFC22 H23 I O3P 21 21 215.7232; 10.8546; 32.913
90; 90; 90		2044.7Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril
Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution.
Organic letters, 2015, 17, 2118-2121
1520300 CIFC36 H46 N4 O2P -17.1052; 14.1156; 16.3735
105.153; 91.858; 102.309		1541.85Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520301 CIFC41 H58.333 N5 OP 1 21/c 126.0651; 15.2582; 9.5468
90; 96.584; 90		3771.8Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520302 CIFC33 H31 Br2 N O6P 1 21/c 118.4779; 9.1189; 19.3437
90; 109.352; 90		3075.2Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J.
Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction.
Organic letters, 2015, 17, 2042-2045
1520303 CIFC13 H23 Cl N2 NiP 1 21/n 111.1164; 12.6843; 11.5897
90; 118.363; 90		1438.02Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G.
A modular, air-stable nickel precatalyst.
Organic letters, 2015, 17, 2166-2169
1520304 CIFC66.33 H81.67 N2 O4 YbP 21 21 2115.592; 20.5827; 60.065
90; 90; 90		19276.4Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming
Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols.
Organic letters, 2015, 17, 2242-2245
1520305 CIFC6 H9 N O4C 1 2/c 116.4651; 6.6186; 14.9686
90; 109.033; 90		1542Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520306 CIFC12 H19 N O3P 1 21/c 111.0623; 9.4884; 11.6015
90; 90.961; 90		1217.56Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520307 CIFC10 H16 B F2 N O3P -19.5474; 11.4938; 11.5223
92.227; 96.964; 91.605		1253.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520308 CIFC12 H20 B F2 N O3P 1 21/n 17.8638; 14.0418; 12.6427
90; 91.6599; 90		1395.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520309 CIFC12 H18 B F2 N O3P 1 21 114.7772; 11.1085; 16.6848
90; 92.405; 90		2736.4Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520310 CIFC13 H20 B F2 N O3P 1 21/n 110.6399; 11.8723; 11.9174
90; 107.028; 90		1439.41Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520311 CIFC12 H18 B F2 N O4P -111.3963; 11.7254; 12.5468
74.986; 64.116; 64.237		1353.47Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520312 CIFC10 H16 B F2 N O4I b a 212.1721; 49.556; 8.341
90; 90; 90		5031.3Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520313 CIFC10 H16 B F2 N O4P -17.0022; 7.7079; 12.3657
83.232; 83.476; 76.265		641.26Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520314 CIFC10 H17 N O4P -17.8792; 8.1476; 10.2749
106.191; 106.585; 104.538		566.58Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520315 CIFC12 H20 B F2 N O4P b c a16.8311; 9.1985; 18.0999
90; 90; 90		2802.24Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520316 CIFC12 H18 B Br2 F2 N O4P 1 21/c 110.3517; 15.7916; 9.5485
90; 99.476; 90		1539.59Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520317 CIFC8 H11 Br O4P 1 21/c 18.8688; 18.0772; 6.0396
90; 94.753; 90		964.96Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520318 CIFC19 H23.6 B F2 N2 O5.3P b c n12.2584; 10.1061; 31.0115
90; 90; 90		3841.8Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520319 CIFC19 H23 B F2 N2 O5P 1 21/n 115.4609; 8.0727; 15.6576
90; 103.611; 90		1899.36Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520320 CIFC30 H25 N2 O4 PP 1 21/c 112.5638; 14.8917; 13.7164
90; 104.477; 90		2484.8Yamamura, Masaki; Takizawa, Hiroyuki; Nabeshima, Tatsuya
Zwitterionic N2O2-Type Protonated Dipyrrin Bearing a Phosphate Anionic Moiety as a pH-Responsive Fluorescence Indicator.
Organic letters, 2015, 17, 3114-3117
1520385 CIFC41 H45 Cl2 N5 O18P -118.718; 20.1801; 21.555
63.466; 65.8; 82.646		6629.1Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520386 CIFC48 H53 N5 O16 S2P 1 21/n 19.5948; 11.7166; 43.6295
90; 91.392; 90		4903.3Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520387 CIFC48 H51 N5 O13 SP 1 21/c 110.656; 38.925; 11.435
90; 111.21; 90		4422Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520388 CIFC22 H19 N O2P 21 21 218.6008; 10.6881; 18.1
90; 90; 90		1663.9Battini, Narsaiah; Battula, Satyanarayana; Kumar, Raju Ranjith; Ahmed, Qazi Naveed
2-Oxo Driven Unconventional reactions: Microwave Assisted Approaches to Tetrahydrofuro[3,2-d]oxazoles and Furanones.
Organic letters, 2015, 17, 2992-2995
1520439 CIFC26 H18 B Cl2 F8 N3P 1 21/c 17.923; 11.039; 27.77
90; 96.981; 90		2410.8Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520440 CIFC26.14 H22.79 B Cl0.79 F2 N3 O3.24P 1 21/c 113.159; 12.065; 15.082
90; 98.075; 90		2370.7Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520441 CIFC707 H656 B16 F32 N48 O9P 1 21/c 115.429; 41.602; 24.49
90; 91.209; 90		15716Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520442 CIFC35.79 H27.57 B Cl1.57 F2 N3C 1 2/c 133.021; 10.588; 23.034
90; 132.89; 90		5900Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520443 CIFC32 H24 B Cl2 F2 N3P -17.3425; 11.0127; 15.884
94.772; 97.467; 91.375		1268.3Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520444 CIFC50.45 H44.9 B Cl2.9 F2 N3P 1 21/c 18.0911; 21.853; 25.007
90; 97.291; 90		4385.9Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520445 CIFC23 H18 B F2 N3P 1 21/n 19.594; 8.7428; 21.526
90; 100.795; 90		1773.6Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520446 CIFC16 H15 N O2 S2P c a 2118.773; 7.8448; 20.3148
90; 90; 90		2991.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520447 CIFC16 H14 F N O2 S2P 1 21/c 115.7817; 13.0488; 7.2719
90; 92.391; 90		1496.2Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520448 CIFC16 H15 N O3 S2P -19.7686; 10.4236; 16.0412
90.974; 91.846; 107.681		1554.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520449 CIFC16 H15 N O2 S SeP b c a7.38023; 12.875; 31.8273
90; 90; 90		3024.24Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520450 CIFC17 H17 N O2 S2P 1 21/n 16.63588; 12.9255; 19.0476
90; 93.665; 90		1630.41Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520451 CIFC40 H32 N2P 1 21/n 112.149; 7.34; 16.53
90; 101.456; 90		1444.7Xu, Feng; Peng, Lifen; Shinohara, Kenta; Nishida, Takanori; Wakamatsu, Kan; Uejima, Motoyuki; Sato, Tohru; Tanaka, Kazuyoshi; Machida, Norihiko; Akashi, Haruo; Orita, Akihiro; Otera, Junzo
One-Shot Double Amination of Sondheimer-Wong Diynes: Synthesis of Photoluminescent Dinaphthopentalenes.
Organic letters, 2015, 17, 3014-3017
1520491 CIFC60 H74 N4 O4P -111.2497; 12.373; 20.0241
95.185; 106.067; 94.622		2651.1Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus
Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide.
Organic letters, 2015, 17, 3074-3077
1520504 CIFC20 H16 I N OP -110.699; 11.726; 22.2683
94.284; 101.795; 109.369		2549Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520505 CIFC20 H16 I N OP b c a7.2355; 20.9295; 23.0167
90; 90; 90		3485.5Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520513 CIFC24 H24P 1 21/n 17.4014; 30.606; 7.739
90; 100.806; 90		1722Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520514 CIFC20 H24 O4 SP 1 n 111.2988; 5.7063; 14.045
90; 102.129; 90		885.3Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520515 CIFC25 H29 N O5 SF d d 222.419; 52.094; 7.523
90; 90; 90		8786Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520516 CIFC25 H29 N O5 SC 1 2/c 130.166; 11.6914; 14.2065
90; 113.297; 90		4601.9Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520517 CIFC19 H19 F OP 21 21 218.4903; 9.6656; 18.663
90; 90; 90		1531.6Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520518 CIFC43 H41 N3 O4P 1 21/c 131.617; 15.428; 14.478
90; 101.899; 90		6910Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke
Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols
Organic Letters, 2015, 17, 3138-3141
1520519 CIFC13 H12 Cl N O4P 21 21 217.9023; 12.49; 12.9
90; 90; 90		1273.2Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo
Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones.
Organic letters, 2015, 17, 3026-3029
1520520 CIFC39 H40 B F2 N3 O4P -18.745; 10.225; 20.19
89.48; 86.38; 65.669		1641.4Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520521 CIFC37.5 H36.5 B Cl1.5 F2 N3 O4P -18.776; 10.567; 19.225
84.193; 82.204; 69.585		1652.6Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520522 CIFC46 H44 B2 N2 O2P 1 21/c 17.274; 17.864; 15.322
90; 100.332; 90		1958.7Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520523 CIFC42 H36 B2 N2 O2P 1 21/c 17.054; 17.672; 13.751
90; 96.406; 90		1703.5Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520542 CIFC32 H25 N O4P 1 21 16.62144; 20.1343; 9.362
90; 100.915; 90		1225.54Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei
Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.
Organic letters, 2015, 17, 3206-3209
1520547 CIFC25 H24 SP -19.4128; 9.6074; 12.0794
97.999; 97.992; 108.357		1007.08Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo
Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides.
Organic letters, 2015, 17, 3322-3325
1520552 CIFC36 H22 N12P 1 21/n 115.3809; 11.5149; 17.7975
90; 90.677; 90		3151.9Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520553 CIFC35 H19 F4 N6 O2 PI b a 221.689; 29.869; 10.7143
90; 90; 90		6941Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520554 CIFC51 H33 Co F4 N8P 1 21/c 112.3996; 15.4999; 21.5037
90; 97.248; 90		4099.8Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520555 CIFC24 H20 Br2 N2C 1 2/c 116.3504; 14.9527; 9.2389
90; 92.387; 90		2256.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520556 CIFC24 H18 N2P -19.4274; 12.3411; 15.5934
83.302; 82.714; 79.24		1759.9Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520557 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.33; 10.8862; 17.8919
90; 110.048; 90		2622Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520558 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.3809; 10.9748; 11.0438
109.43; 98.185; 97.328		1153.7Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520559 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.4495; 11.0503; 11.0576
109.671; 96.586; 97.962		1172.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520560 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.369; 10.925; 18.106
90; 110.574; 90		2661Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520561 CIFC51 H58 F6 O14 S2P -111.2709; 11.7647; 20.1194
88.271; 83.035; 86.352		2642.1Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520562 CIFC46 H46 Cl2 F6 O14 S2P 1 n 111.616; 18.2419; 11.617
90; 94.1589; 90		2455.14Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520563 CIFC48.75 H55.04 Cl2.25 F3 O12 SP n a 2135.9931; 12.0648; 11.369
90; 90; 90		4937Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520564 CIFC51 H58 F6 O14 S2P 21 21 2111.3045; 12.1357; 37.187
90; 90; 90		5101.6Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520565 CIFC51 H55 F9 O16 S3P 1 21/c 122.0373; 11.9982; 22.7155
90; 110.288; 90		5633.5Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520566 CIFC51 H55 F9 O16 S3P b c a20.6289; 22.2856; 24.1696
90; 90; 90		11111.4Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520573 CIFC17 H15 N SP 21 21 216.1669; 12.182; 17.8605
90; 90; 90		1341.77Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520574 CIFC19 H17 N OP b c a7.4565; 18.3137; 20.6855
90; 90; 90		2824.73Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520575 CIFC16 H15 N3P 1 21/m 19.7773; 6.90436; 9.79548
90; 98.985; 90		653.14Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520576 CIFC21 H15 N3P 1 21/c 114.0946; 11.4421; 9.74761
90; 99.2056; 90		1551.77Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520577 CIFC20 H20 O6P 21 21 2110.1756; 12.2477; 13.4918
90; 90; 90		1681.45Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo
Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells.
Organic letters, 2015, 17, 3280-3282
1520614 CIFC25 H23 N O3P 1 21/c 19.4141; 23.293; 9.0609
90; 92.942; 90		1984.3Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520615 CIFC18 H17 N O2P 1 21/c 18.0166; 15.8594; 11.2674
90; 98.788; 90		1415.7Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520616 CIFC37 H31 N O5P 1 21/n 111.364; 10.93; 24.447
90; 96.564; 90		3017Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun
Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes.
Organic letters, 2015, 17, 3314-3317
1520633 CIFC22 H21 Br N2 O3 S2P b c a11.7745; 15.3391; 24.3582
90; 90; 90		4399.34Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520634 CIFC22 H20 N2 O4 S2P -19.0038; 10.66; 11.8108
75.2664; 76.0323; 75.5364		1042.26Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520635 CIFC30 H29 N O3P 21 21 217.37176; 14.7771; 21.8173
90; 90; 90		2376.63Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520636 CIFC29 H32 N2 S2P 1 21 110.39896; 9.11807; 13.7409
90; 108.291; 90		1237.06Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520637 CIFC21 H15 F O2P 1 21/c 112.0845; 5.9453; 22.597
90; 103.246; 90		1580.3Du, Xiang-Wei; Stanley, Levi M.
Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives.
Organic letters, 2015, 17, 3276-3279
1520655 CIFC32 H38 O5 Si2P 1 21/c 19.2692; 9.7098; 34.752
90; 92.266; 90		3125.3Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520656 CIFC16 H17 Cl O5P -16.9648; 7.7685; 14.728
76.228; 76.658; 84.002		752.04Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520657 CIFC18 H17 Br O5P 1 21 15.6762; 10.5443; 14.1611
90; 100.294; 90		833.92Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K.
Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade.
Organic letters, 2015, 17, 3302-3305
1520658 CIFC19 H20 N2 O6P 21 21 215.8624; 9.6327; 31.868
90; 90; 90		1799.61Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers.
Organic letters, 2015, 17, 3248-3251
1520659 CIFC22 H32 Cl2 I2 Si2P 1 21/n 113.1915; 9.4009; 22.0383
90; 106.275; 90		2623.49Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520660 CIFC16 H10 Cl2 I2P b c a9.0806; 15.5457; 23.2185
90; 90; 90		3277.6Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520682 CIFC26 H19 N3 O5 SP -110.4761; 10.8361; 11.3358
76.911; 61.867; 86.563		1103.68Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng
Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates.
Organic letters, 2015, 17, 3552-3555
1520683 CIFC20 H24 Cl N3 OP 1 21 110.868; 6.8325; 12.6102
90; 103.793; 90		909.38Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond
Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Organic letters, 2015, 17, 3474-3477
1520684 CIFC13 H17 Cl O3P n a 2128.508; 5.4891; 8.1976
90; 90; 90		1282.79Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520685 CIFC21 H21 Cl O4P b c a15.5081; 11.7102; 20.245
90; 90; 90		3676.6Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520686 CIFC33 H30 N2 O6 S2P -110.7946; 12.4093; 13.1553
76.627; 68.739; 81.216		1593.12Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng
Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3536-3539
1520694 CIFC33 H27 N3 O13P -111.319; 12.665; 14.597
86.284; 86.306; 68.207		1937.1Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun
Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization.
Organic letters, 2015, 17, 3379-3381
1520702 CIFC41 H60 N8 O3 Ti2P 1 21/n 119.8643; 9.0349; 24.8875
90; 106.793; 90		4276.1Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520703 CIFC163 H221 N28 O13 Ti4P -119.976; 20.518; 21.236
89.583; 78.919; 76.303		8292Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520704 CIFC22 H20 N2 O3P -111.7148; 11.8534; 14.1205
110; 95.83; 100.677		1781.51Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520705 CIFC22 H22 N2 O3P c a 2117.651; 15.5231; 13.7865
90; 90; 90		3777.48Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520706 CIFC22 H20 N2 O3P 1 21/n 115.2406; 5.6664; 20.6863
90; 94.254; 90		1781.53Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520707 CIFC20 H23 N O8P 21 21 218.7215; 11.3257; 19.217
90; 90; 90		1898.2Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A.
Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol.
Organic letters, 2015, 17, 3422-3425
1520708 CIFC15 H15 N3 O4P 1 21/n 111.4762; 7.95324; 16.5869
90; 107.894; 90		1440.7Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang
(+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata.
Organic letters, 2015, 17, 3458-3461
1520726 CIFC44 H42 F6 N6 O7 S2P b c a21.512; 10.424; 40.881
90; 90; 90		9167Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520727 CIFC28 H23 F3 N2 O3P -18.882; 10.743; 14.629
87; 76.43; 65.66		1234.8Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520728 CIFC25 H34 N2 O9 SiP b c a10.3059; 20.6482; 25.5756
90; 90; 90		5442.4Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P.
Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes.
Organic letters, 2015, 17, 3568-3571
1520729 CIFC25 H31 N O3 S2P 1 21 16.6067; 19.709; 9.7407
90; 109.22; 90		1197.65Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè
Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2.
Organic letters, 2015, 17, 3540-3543
1520753 CIFC13 H13 Cl N2 O2 SP 1 21/c 115.767; 5.759; 15.721
90; 112.32; 90		1320.5Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng
Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols.
Organic letters, 2015, 17, 2350-2353
1520754 CIFC23 H21 N O3 S2P -17.667; 8.7269; 17.0497
88.1161; 89.15; 62.1966		1008.54Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro
Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.
Organic letters, 2015, 17, 2454-2457
1520755 CIFC270 H372 B6 N8 O30C 1 2/c 152.579; 21.835; 29.598
90; 117.54; 90		30130Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1520756 CIFC28 H44 O4 Si2P 21 21 217.702; 13.1321; 27.4999
90; 90; 90		2781.4Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2342-2345

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