Crystallography Open Database

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1543142 CIFC90 H21 Cl F5 NP -113.9563; 14.4188; 15.4405
91.044; 108.456; 109.296		2755.5Lou, Ning; Li, Yanbang; Cui, Chengxing; Liu, Yajun; Gan, Liangbing
Preparation of Azafullerene C59NR5 and Fullerene Derivative C60NAr5 with a Pyridine Moiety on the Cage Skeleton.
Organic letters, 2016, 18, 2236-2239
1543151 CIFC19 H30 O2C 1 2/c 126.8752; 11.059; 12.0165
90; 111.962; 90		3312.28Parthasarathy, Gowrisankar; Eggert, Ulrike; Kalesse, Markus
Synthesis of (+)-Omphadiol and (+)-Pyxidatol C.
Organic letters, 2016, 18, 2320-2322
1543156 CIFC20 H24 N4 O4P -17.8318; 10.2287; 13.5191
108.782; 106.051; 94.161		969.7Reekie, Tristan A.; Donckele, Etienne J.; Manenti, Giorgio; Püntener, Salome; Trapp, Nils; Diederich, François
A Three-Step Synthesis of Tetrasubstituted NH-Pyrroles.
Organic letters, 2016, 18, 2252-2255
1543157 CIFC22 H28 N4 O4P 1 21/c 115.0264; 19.058; 15.9395
90; 112.057; 90		4230.6Reekie, Tristan A.; Donckele, Etienne J.; Manenti, Giorgio; Püntener, Salome; Trapp, Nils; Diederich, François
A Three-Step Synthesis of Tetrasubstituted NH-Pyrroles.
Organic letters, 2016, 18, 2252-2255
1543158 CIFC20 H23 N3 O4 SP 1 21 18.514; 22.5; 11.0395
90; 107.154; 90		2020.71Reekie, Tristan A.; Donckele, Etienne J.; Manenti, Giorgio; Püntener, Salome; Trapp, Nils; Diederich, François
A Three-Step Synthesis of Tetrasubstituted NH-Pyrroles.
Organic letters, 2016, 18, 2252-2255
1543159 CIFC20 H22 N4 O6P 1 21/c 19.5426; 13.1663; 16.2954
90; 101.215; 90		2008.3Reekie, Tristan A.; Donckele, Etienne J.; Manenti, Giorgio; Püntener, Salome; Trapp, Nils; Diederich, François
A Three-Step Synthesis of Tetrasubstituted NH-Pyrroles.
Organic letters, 2016, 18, 2252-2255
1543160 CIFC26 H20 OP -18.8; 10.295; 21.034
90.156; 93.24; 91.754		1902Luo, Lei; Zheng, Huayu; Liu, Jingjing; Wang, Hui; Wang, Yaoyu; Luan, Xinjun
Highly Chemo- and Regioselective Construction of Spirocarbocycles by a Pd(0)-Catalyzed Dearomatization of Phenol-Based Biaryls with 1,3-Dienes.
Organic letters, 2016, 18, 2082-2085
1543161 CIFC28 H40 O5P 21 21 218.7878; 20.2223; 29.819
90; 90; 90		5299.1Hu, Linzhen; Zhang, Yu; Zhu, Hucheng; Liu, Junjun; Li, Hua; Li, Xiao-Nian; Sun, Weiguang; Zeng, Junfen; Xue, Yongbo; Zhang, Yonghui
Filicinic Acid Based Meroterpenoids with Anti-Epstein-Barr Virus Activities from Hypericum japonicum.
Organic letters, 2016, 18, 2272-2275
1543162 CIFC17 H13 N O3 SP 1 21/c 121.2968; 7.11439; 21.9163
90; 108.646; 90		3146.32Chen, Ming; Yang, Chao; Wang, Yanpei; Li, Dazhi; Xia, Wujiong
UV Light Induced Direct Synthesis of Phenanthrene Derivatives from a Linear 3-Aryl-N-(arylsulfonyl) Propiolamides.
Organic letters, 2016, 18, 2280-2283
1543163 CIFC16 H10 F N O3 SP 1 21 16.8436; 10.3886; 9.9058
90; 104.893; 90		680.6Chen, Ming; Yang, Chao; Wang, Yanpei; Li, Dazhi; Xia, Wujiong
UV Light Induced Direct Synthesis of Phenanthrene Derivatives from a Linear 3-Aryl-N-(arylsulfonyl) Propiolamides.
Organic letters, 2016, 18, 2280-2283
1543164 CIFC71 H66P -111.5438; 13.25; 19.248
84.314; 82.576; 64.917		2640.9Uchida, Yosuke; Hirose, Takashi; Nakashima, Takuya; Kawai, Tsuyoshi; Matsuda, Kenji
Synthesis and Photophysical Properties of a 13,13'-Bibenzo[b]perylenyl Derivative as a π-Extended 1,1'-Binaphthyl Analog.
Organic letters, 2016, 18, 2118-2121
1543214 CIFC25 H21 N O4P 1 21/c 16.1861; 14.2021; 22.962
90; 94.024; 90		2012.37El Bouakher, Abderrahman; Le Goff, Ronan; Tasserie, Jordan; Lhoste, Jérôme; Martel, Arnaud; Comesse, Sébastien
Synthesis of Oxazolidin-4-ones: Domino O-Alkylation/Aza-Michael/Intramolecular Retro-Claisen Condensation.
Organic letters, 2016, 18, 2383-2386
1543215 CIFC17 H21 N O5P 1 21/c 17.8917; 22.2343; 9.4685
90; 91.94; 90		1660.5El Bouakher, Abderrahman; Le Goff, Ronan; Tasserie, Jordan; Lhoste, Jérôme; Martel, Arnaud; Comesse, Sébastien
Synthesis of Oxazolidin-4-ones: Domino O-Alkylation/Aza-Michael/Intramolecular Retro-Claisen Condensation.
Organic letters, 2016, 18, 2383-2386
1543216 CIFC24 H27 N O7P c a 2122.7748; 6.0842; 16.1449
90; 90; 90		2237.1El Bouakher, Abderrahman; Le Goff, Ronan; Tasserie, Jordan; Lhoste, Jérôme; Martel, Arnaud; Comesse, Sébastien
Synthesis of Oxazolidin-4-ones: Domino O-Alkylation/Aza-Michael/Intramolecular Retro-Claisen Condensation.
Organic letters, 2016, 18, 2383-2386
1543217 CIFC20 H21 N O5 SP 1 21/n 17.795; 21.513; 11.4883
90; 95.42; 90		1917.9El Bouakher, Abderrahman; Le Goff, Ronan; Tasserie, Jordan; Lhoste, Jérôme; Martel, Arnaud; Comesse, Sébastien
Synthesis of Oxazolidin-4-ones: Domino O-Alkylation/Aza-Michael/Intramolecular Retro-Claisen Condensation.
Organic letters, 2016, 18, 2383-2386
1543218 CIFC22 H23 N O5P 17.8503; 11.0271; 17.767
75.302; 81.673; 89.125		1471.6El Bouakher, Abderrahman; Le Goff, Ronan; Tasserie, Jordan; Lhoste, Jérôme; Martel, Arnaud; Comesse, Sébastien
Synthesis of Oxazolidin-4-ones: Domino O-Alkylation/Aza-Michael/Intramolecular Retro-Claisen Condensation.
Organic letters, 2016, 18, 2383-2386
1543219 CIFC36 H44 Cl2 N4 O2 RuP 1 21/n 111.9275; 15.7557; 18.3669
90; 97.6486; 90		3420.9Williams, Michael J.; Kong, Jongrock; Chung, Cheol K.; Brunskill, Andrew; Campeau, Louis-Charles; McLaughlin, Mark
The Discovery of Quinoxaline-Based Metathesis Catalysts from Synthesis of Grazoprevir (MK-5172).
Organic letters, 2016, 18, 1952-1955
1543235 CIFC22 H19 N OP b c a14.2222; 12.0292; 19.1416
90; 90; 90		3274.8Gu, Zheng-Yang; Liu, Cheng-Guo; Wang, Shun-Yi; Ji, Shun-Jun
Pd-Catalyzed Intramolecular Heck Reaction, C(sp(2))-H Activation, 1,4-Pd Migration, and Aminopalladation: Chemoselective Synthesis of Dihydroindeno[1,2,3-kl]acridines and 3-Arylindoles.
Organic letters, 2016, 18, 2379-2382
1543236 CIFC20 H14 F NP 1 21/c 18.9782; 18.2579; 17.6665
90; 101.906; 90		2833.6Gu, Zheng-Yang; Liu, Cheng-Guo; Wang, Shun-Yi; Ji, Shun-Jun
Pd-Catalyzed Intramolecular Heck Reaction, C(sp(2))-H Activation, 1,4-Pd Migration, and Aminopalladation: Chemoselective Synthesis of Dihydroindeno[1,2,3-kl]acridines and 3-Arylindoles.
Organic letters, 2016, 18, 2379-2382
1543237 CIFC40 H26 F3 N O3 SC 1 2/c 126.374; 7.9979; 15.0584
90; 99.855; 90		3129.5Ge, Qingmei; Hu, Yang; Li, Bin; Wang, Baiquan
Synthesis of Conjugated Polycyclic Quinoliniums by Rhodium(III)-Catalyzed Multiple C-H Activation and Annulation of Arylpyridiniums with Alkynes.
Organic letters, 2016, 18, 2483-2486
1543260 CIFC12 H11 N O2 S2P -16.6545; 7.7124; 12.1476
87.201; 88.293; 71.09		589.03Shukla, Gaurav; Srivastava, Abhijeet; Singh, Maya Shankar
Metal- and Catalyst-Free, Formal [4 + 1] Annulation via Tandem C═O/C═S Functionalization: One-Pot Access to 3,5-Disubstituted/Annulated Isothiazoles.
Organic letters, 2016, 18, 2451-2454
1543261 CIFC26 H21 F N2 O4 SP -19.8714; 11.0898; 12.4017
75.477; 84.873; 77.924		1284.2Cheng, Dong; Ling, Fei; Zheng, Chenguang; Ma, Cheng
Tuning of Copper-Catalyzed Multicomponent Reactions toward 3-Functionalized Oxindoles.
Organic letters, 2016, 18, 2435-2438
1543262 CIFC26 H24 N2 O5 SP 1 21/n 112.8999; 8.74; 20.7336
90; 92.1223; 90		2336.01Cheng, Dong; Ling, Fei; Zheng, Chenguang; Ma, Cheng
Tuning of Copper-Catalyzed Multicomponent Reactions toward 3-Functionalized Oxindoles.
Organic letters, 2016, 18, 2435-2438
1543263 CIFC28 H22 N2 O4 SP -19.8063; 11.6743; 12.6069
117.544; 101.784; 99.146		1198.13Cheng, Dong; Ling, Fei; Zheng, Chenguang; Ma, Cheng
Tuning of Copper-Catalyzed Multicomponent Reactions toward 3-Functionalized Oxindoles.
Organic letters, 2016, 18, 2435-2438
1543264 CIFC28 H21 F N2 O4 SP 1 21/c 110.3056; 14.0546; 17.9127
90; 106.449; 90		2488.3Cheng, Dong; Ling, Fei; Zheng, Chenguang; Ma, Cheng
Tuning of Copper-Catalyzed Multicomponent Reactions toward 3-Functionalized Oxindoles.
Organic letters, 2016, 18, 2435-2438
1543269 CIFC23 H16 Br N O2C 1 2/c 117.9232; 12.4144; 19.2095
90; 116.795; 90		3815.3Xu, Ning; Gu, Da-Wei; Zi, Jing; Wu, Xin-Yan; Guo, Xun-Xiang
Enantioselective Synthesis of 3-Alkynyl-3-hydroxyindolin-2-ones by Copper-Catalyzed Asymmetric Addition of Terminal Alkynes to Isatins.
Organic letters, 2016, 18, 2439-2442
1543270 CIFC16 H14 N2P 1 21/a 113.8715; 5.5938; 17.2693
90; 113.43; 90		1229.51Ho, Hon Eong; Oniwa, Kazuaki; Yamamoto, Yoshinori; Jin, Tienan
N-Methyl Transfer Induced Copper-Mediated Oxidative Diamination of Alkynes.
Organic letters, 2016, 18, 2487-2490
1543303 CIFC25 H18 Cl3 N3 O8C 1 2/c 129.8039; 9.4923; 22.1375
90; 120.796; 90		5379.8Barros, Stephanie A.; Yoon, Ina; Suh, Sung-Eun; Chenoweth, David M.
Bridgehead-Substituted Triptycenes for Discovery of Nucleic Acid Junction Binders.
Organic letters, 2016, 18, 2423-2426
1543304 CIFC10 H12 N2 OP b c a13.6534; 6.92272; 18.544
90; 90; 90		1752.75Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543305 CIFC12 H16 N2 OP 1 21/c 16.3014; 11.7426; 15.4771
90; 100.561; 90		1125.82Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543306 CIFC22 H27 N3 O3P 21 21 219.3255; 10.2652; 20.1671
90; 90; 90		1930.56Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543307 CIFC9 H10 N2 OP 1 21/n 17.0381; 13.3229; 8.7353
90; 112.215; 90		758.29Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543308 CIFC61 H58 Cu F6 N2 O P3P 1 21 112.8125; 15.5638; 16.7344
90; 110.994; 90		3115.51Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543309 CIFC22 H26 F N3 O3P 21 21 219.11599; 13.3173; 34.5039
90; 90; 90		4188.79Arteaga, Fernando Arteaga; Liu, Zijian; Brewitz, Lennart; Chen, Jianyang; Sun, Bo; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Mannich-Type Reaction of Alkylamides.
Organic letters, 2016, 18, 2391-2394
1543317 CIFC24 H19 Br N2 O2 SP 111.3141; 13.0066; 13.3059
107.027; 97.7315; 113.173		1650.25Kikuchi, Jun; Momiyama, Norie; Terada, Masahiro
Chiral Phosphoric Acid Catalyzed Diastereo- and Enantioselective Mannich-Type Reaction between Enamides and Thiazolones.
Organic letters, 2016, 18, 2521-2523
1543332 CIFC29 H27 N O4 SP 21 21 218.3536; 13.8716; 21.444
90; 90; 90		2484.9Zhang, Yu-Fang; Chen, Diao; Chen, Wen-Wen; Xu, Ming-Hua
Construction of Cyclic Sulfamidates Bearing Two gem-Diaryl Stereocenters through a Rhodium-Catalyzed Stepwise Asymmetric Arylation Protocol.
Organic letters, 2016, 18, 2726-2729
1543337 CIFC9 H6 F2 I N OP 1 21/n 15.9943; 8.2991; 20.452
90; 97.16; 90		1009.5Miao, Wenjun; Ni, Chuanfa; Zhao, Yanchuan; Hu, Jinbo
Nucleophilic Iododifluoromethylation of Carbonyl Compounds Using Difluoromethyl 2-Pyridyl Sulfone.
Organic letters, 2016, 18, 2766-2769
1543338 CIFC23 H17 Br O3P 1 21 15.4774; 14.656; 11.788
90; 103.09; 90		921.7Zhou, Yong; Zhu, Fu-Lin; Liu, Zhen-Ting; Zhou, Xiao-Mao; Hu, Xiang-Ping
Chiral Ferrocenyl P,N-Ligands for Palladium-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Propargylic Esters with β-Ketoesters: Access to Functionalized Chiral 2,3-Dihydrofurans.
Organic letters, 2016, 18, 2734-2737
1543339 CIFC35 H38 Fe N3 O PP 21 21 2110.678; 10.701; 27.346
90; 90; 90		3124.7Zhou, Yong; Zhu, Fu-Lin; Liu, Zhen-Ting; Zhou, Xiao-Mao; Hu, Xiang-Ping
Chiral Ferrocenyl P,N-Ligands for Palladium-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Propargylic Esters with β-Ketoesters: Access to Functionalized Chiral 2,3-Dihydrofurans.
Organic letters, 2016, 18, 2734-2737
1543356 CIFC29 H22 O4P 15.105; 9.985; 11.8359
65.909; 85.15; 82.591		545.829Aida, Yukimasa; Sugiyama, Haruki; Uekusa, Hidehiro; Shibata, Yu; Tanaka, Ken
Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of α,ω-Diynes with Unsymmetrical 1,2-Disubstituted Alkenes.
Organic letters, 2016, 18, 2672-2675
1543357 CIFC18 H14 I N3 SP -18.0454; 9.1035; 11.6624
91.647; 96.901; 93.582		845.76Yamamoto, Kosuke; Bruun, Theodora; Kim, Jung Yun; Zhang, Lei; Lautens, Mark
A New Multicomponent Multicatalyst Reaction (MC)(2)R: Chemoselective Cycloaddition and Latent Catalyst Activation for the Synthesis of Fully Substituted 1,2,3-Triazoles.
Organic letters, 2016, 18, 2644-2647
1543359 CIFC20 H25 N O2P 1 21 19.3889; 11.6277; 16.0269
90; 96.069; 90		1739.9Fernández-Pérez, Héctor; Lao, Joan R.; Vidal-Ferran, Anton
Stereoselective Rh-Catalyzed Hydrogenative Desymmetrization of Achiral Substituted 1,4-Dienes.
Organic letters, 2016, 18, 2836-2839
1543360 CIFC21 H24 O4P 21 21 215.87215; 17.2976; 17.9057
90; 90; 90		1818.76Manaviazar, Soraya; Nockemann, Peter; Hale, Karl J.
Total Synthesis of the GRP78-Downregulatory Macrolide (+)-Prunustatin A, the Immunosuppressant (+)-SW-163A, and a JBIR-04 Diastereoisomer That Confirms JBIR-04 Has Nonidentical Stereochemistry to (+)-Prunustatin A.
Organic letters, 2016, 18, 2902-2905
1543361 CIFC13 H16 O3P 1 21 18.246; 6.3133; 11.1291
90; 97.945; 90		573.81Manaviazar, Soraya; Nockemann, Peter; Hale, Karl J.
Total Synthesis of the GRP78-Downregulatory Macrolide (+)-Prunustatin A, the Immunosuppressant (+)-SW-163A, and a JBIR-04 Diastereoisomer That Confirms JBIR-04 Has Nonidentical Stereochemistry to (+)-Prunustatin A.
Organic letters, 2016, 18, 2902-2905
1543362 CIFC33 H43 N O12P 21 21 227.6917; 14.8522; 8.87923
90; 90; 90		3651.87Manaviazar, Soraya; Nockemann, Peter; Hale, Karl J.
Total Synthesis of the GRP78-Downregulatory Macrolide (+)-Prunustatin A, the Immunosuppressant (+)-SW-163A, and a JBIR-04 Diastereoisomer That Confirms JBIR-04 Has Nonidentical Stereochemistry to (+)-Prunustatin A.
Organic letters, 2016, 18, 2902-2905
1543363 CIFC31 H43 N O11P 21 21 227.6917; 14.8522; 8.87923
90; 90; 90		3651.87Manaviazar, Soraya; Nockemann, Peter; Hale, Karl J.
Total Synthesis of the GRP78-Downregulatory Macrolide (+)-Prunustatin A, the Immunosuppressant (+)-SW-163A, and a JBIR-04 Diastereoisomer That Confirms JBIR-04 Has Nonidentical Stereochemistry to (+)-Prunustatin A.
Organic letters, 2016, 18, 2902-2905
1543364 CIFC28 H48 O3 Si2C 1 2/c 148.523; 6.2947; 20.561
90; 107.18; 90		6000Rullière, Pauline; Grisel, Julien; Poittevin, Clément; Cividino, Pascale; Carret, Sébastien; Poisson, Jean-François
Thermal [2 + 2]-Cycloaddition of Ketenes with Chiral Enol Ethers: Route to Densely Substituted Cyclobutanones.
Organic letters, 2016, 18, 2824-2827
1543365 CIFC20 H26 O3P 21 21 216.66247; 16.2362; 16.4824
90; 90; 90		1782.95Fei, Dong-Qing; Dong, Le-Le; Qi, Feng-Ming; Fan, Gai-Xia; Li, Hui-Hong; Li, Zheng-Yu; Zhang, Zhan-Xin
Euphorikanin A, a Diterpenoid Lactone with a Fused 5/6/7/3 Ring System from Euphorbia kansui.
Organic letters, 2016, 18, 2844-2847
1543366 CIFC18.5 H22 Cl N O8P b c a7.5805; 17.2484; 32.295
90; 90; 90		4222.62Zhou, Qing-Fa; Zhang, Kui; Cai, Lingchao; Kwon, Ohyun
Phosphine-Catalyzed Intramolecular Cyclizations of α-Nitroethylallenoates Forming (Z)-Furanone Oximes.
Organic letters, 2016, 18, 2954-2957
1543389 CIFC9 H11 N O5P 1 21 18.0163; 5.9409; 10.63
90; 108.56; 90		479.91Gutiérrez-Jiménez, Marta I; Aydillo, Carlos; Navo, Claudio D.; Avenoza, Alberto; Corzana, Francisco; Jiménez-Osés, Gonzalo; Zurbano, María M; Busto, Jesús H; Peregrina, Jesús M
Bifunctional Chiral Dehydroalanines for Peptide Coupling and Stereoselective S-Michael Addition.
Organic letters, 2016, 18, 2796-2799
1543390 CIFC25 H36 Cl4 N2 O13 SP 21 21 2110.6272; 12.262; 25.592
90; 90; 90		3334.9Gutiérrez-Jiménez, Marta I; Aydillo, Carlos; Navo, Claudio D.; Avenoza, Alberto; Corzana, Francisco; Jiménez-Osés, Gonzalo; Zurbano, María M; Busto, Jesús H; Peregrina, Jesús M
Bifunctional Chiral Dehydroalanines for Peptide Coupling and Stereoselective S-Michael Addition.
Organic letters, 2016, 18, 2796-2799
1543395 CIFC17 H20 F3 N O3P 1 21/c 110.019; 9.396; 19.802
90; 112.805; 90		1718.4Cheng, Cungui; Liu, Shuiyou; Lu, Danyang; Zhu, Gangguo
Copper-Catalyzed Trifluoromethylation of Alkenes with Redox-Neutral Remote Amidation of Aldehydes.
Organic letters, 2016, 18, 2852-2855
1543396 CIFC26 H21 N3P 1 21/n 112.52; 11.4587; 13.5749
90; 93.825; 90		1943.16Mikshiev, Vladimir Y.; Antonov, Alexander S.; Pozharskii, Alexander F.
Tandem Synthesis of 10-Dimethylaminobenzo[h]quinazolines from 2-Ketimino-1,8-bis(dimethylamino)naphthalenes via Nucleophilic Replacement of the Unactivated Aromatic NMe2 Group.
Organic letters, 2016, 18, 2872-2875
1543397 CIFC26 H20 Br N3C 1 2/c 120.8133; 12.4608; 16.5347
90; 106.576; 90		4110.1Mikshiev, Vladimir Y.; Antonov, Alexander S.; Pozharskii, Alexander F.
Tandem Synthesis of 10-Dimethylaminobenzo[h]quinazolines from 2-Ketimino-1,8-bis(dimethylamino)naphthalenes via Nucleophilic Replacement of the Unactivated Aromatic NMe2 Group.
Organic letters, 2016, 18, 2872-2875
1543398 CIFC16 H13 N3 OP c a 2119.0121; 4.9106; 14.288
90; 90; 90		1333.94Senadi, Gopal Chandru; Gore, Babasaheb Sopan; Hu, Wan-Ping; Wang, Jeh-Jeng
BF3-Etherate-Promoted Cascade Reaction of 2-Alkynylanilines with Nitriles: One-Pot Assembly of 4-Amido-Cinnolines.
Organic letters, 2016, 18, 2890-2893
1543399 CIFC18 H19 N O3P 1 21/c 112.0363; 17.5689; 14.3807
90; 99.574; 90		2998.7Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543400 CIFC15 H15 N OP b c a9.7259; 12.0868; 19.6834
90; 90; 90		2313.9Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543401 CIFC18 H19 N O3P b c a13.6505; 13.7482; 15.8641
90; 90; 90		2977.2Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543402 CIFC20 H21 N O2P -19.9913; 11.2227; 14.6382
84.38; 84.025; 81.612		1609.27Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543403 CIFC20 H21 N O2P -110.1906; 12.049; 14.4573
110.513; 90.495; 93.15		1659.4Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543404 CIFC15 H15 N OP 1 21/c 110.7025; 5.6536; 19.5304
90; 96.79; 90		1173.45Pusch, Stefan; Schollmeyer, Dieter; Opatz, Till
A Light-Induced Vinylogous Nazarov-Type Cyclization.
Organic letters, 2016, 18, 3043-3045
1543405 CIFC18 H19 NP b c a15.415; 8.1212; 21.625
90; 90; 90		2707.2Stepherson, Jacob R.; Ayala, Caitlan E.; Tugwell, Thomas H.; Henry, Jeffrey L.; Fronczek, Frank R.; Kartika, Rendy
Carbazole Annulation via Cascade Nucleophilic Addition-Cyclization Involving 2-(Silyloxy)pentadienyl Cation.
Organic letters, 2016, 18, 3002-3005
1543406 CIFC17 H17 NI b a 215.4841; 20.8131; 7.9546
90; 90; 90		2563.5Stepherson, Jacob R.; Ayala, Caitlan E.; Tugwell, Thomas H.; Henry, Jeffrey L.; Fronczek, Frank R.; Kartika, Rendy
Carbazole Annulation via Cascade Nucleophilic Addition-Cyclization Involving 2-(Silyloxy)pentadienyl Cation.
Organic letters, 2016, 18, 3002-3005
1543407 CIFC15 H17 Br N2 O4 SP 1 21/n 115.0538; 6.7288; 16.4896
90; 97.322; 90		1656.68Seitz, Tobias; Fu, Peng; Haut, Franz-Lucas; Adam, Lutz; Habicht, Marija; Lentz, Dieter; MacMillan, John B.; Christmann, Mathias
One-Pot Synthesis of 5-Hydroxy-4H-1,3-thiazin-4-ones: Structure Revision, Synthesis, and NMR Shift Dependence of Thiasporine A.
Organic letters, 2016, 18, 3070-3073
1543408 CIFC15 H17 Br N2 O4 SP 1 21/n 16.2837; 19.6717; 13.8626
90; 95.1; 90		1706.8Seitz, Tobias; Fu, Peng; Haut, Franz-Lucas; Adam, Lutz; Habicht, Marija; Lentz, Dieter; MacMillan, John B.; Christmann, Mathias
One-Pot Synthesis of 5-Hydroxy-4H-1,3-thiazin-4-ones: Structure Revision, Synthesis, and NMR Shift Dependence of Thiasporine A.
Organic letters, 2016, 18, 3070-3073
1543409 CIFC24 H22 N6 O3 PdP 1 21 110.222; 20.4529; 11.0286
90; 102.19; 90		2253.76Ye, Xiaohan; Xu, Chang; Wojtas, Lukasz; Akhmedov, Novruz G.; Chen, Hao; Shi, Xiaodong
Silver-Free Palladium-Catalyzed sp(3) and sp(2) C-H Alkynylation Promoted by a 1,2,3-Triazole Amine Directing Group.
Organic letters, 2016, 18, 2970-2973
1543410 CIFC20 H20 N2 O7 S2P -18.1204; 11.3745; 11.7323
79.619; 85.682; 81.305		1052.38Martínez, Claudio; Pérez, Edwin G; Iglesias, Álvaro; Escudero-Adán, Eduardo C; Muñiz, Kilian
Regioselective Intermolecular Diamination and Aminooxygenation of Alkenes with Saccharin.
Organic letters, 2016, 18, 2998-3001
1543411 CIFC47 H34 Cl2 N6 O20 Pd3 S6P -111.6132; 11.8042; 22.2493
86.411; 75.439; 84.592		2936.5Martínez, Claudio; Pérez, Edwin G; Iglesias, Álvaro; Escudero-Adán, Eduardo C; Muñiz, Kilian
Regioselective Intermolecular Diamination and Aminooxygenation of Alkenes with Saccharin.
Organic letters, 2016, 18, 2998-3001
1543437 CIFC21 H23 F4 N2 O2 SP 1 21 114.501; 8.8433; 17.883
90; 107.206; 90		2190.6Xie, Chen; Zhang, Lijun; Sha, Wanxing; Soloshonok, Vadim A.; Han, Jianlin; Pan, Yi
Detrifluoroacetylative in Situ Generation of Free 3-Fluoroindolin-2-one-Derived Tertiary Enolates: Design, Synthesis, and Assessment of Reactivity toward Asymmetric Mannich Reactions.
Organic letters, 2016, 18, 3270-3273
1543438 CIFC19 H19 N O2P 21 21 215.9339; 12.3047; 21.7128
90; 90; 90		1585.36Jiang, Xiaojian; Yang, Junjie; Zhang, Feng; Yu, Pei; Yi, Peng; Sun, Yewei; Wang, Yuqiang
Synthesis of Quaternary 3,3-Disubstituted 2-Oxindoles from 2-Substituted Indole Using Selectfluor.
Organic letters, 2016, 18, 3154-3157
1543496 CIFC58 H56 O20P 1 n 17.7437; 24.157; 14.585
90; 91.656; 90		2727.2Ren, Wen-Sheng; Zhao, Liang; Wang, Mei-Xiang
Functionalized O6-Corona[6]arenes: Synthesis, Structure, and Fullerene Complexation Property.
Organic letters, 2016, 18, 3126-3129
1543502 CIFC12 H11 Br O4P 21 21 214.435; 5.4251; 48.735
90; 90; 90		1172.58Ghosh, Arun K.; Nyalapatla, Prasanth R.
Correction to Enantioselective Total Synthesis of (+)-Amphirionin-4.
Organic letters, 2016, 18, 3509
1543526 CIFC35 H38 O15 SP 21 21 2113.5014; 15.6835; 16.226
90; 90; 90		3435.8Che, Qian; Tan, Hongsheng; Han, Xiaoning; Zhang, Xiaomin; Gu, Qianqun; Zhu, Tianjiao; Li, Dehai
Naquihexcin A, a S-Bridged Pyranonaphthoquinone Dimer Bearing an Unsaturated Hexuronic Acid Moiety from a Sponge-Derived Streptomyces sp. HDN-10-293.
Organic letters, 2016, 18, 3358-3361
1543527 CIFC20 H15 N O2 SP b c a10.7582; 15.1305; 20.2832
90; 90; 90		3301.64Chen, Fei; Meng, Qiang; Han, Shang-Qing; Han, Bing
tert-Butyl Hydroperoxide (TBHP)-Initiated Vicinal Sulfonamination of Alkynes: A Radical Annulation toward 3-Sulfonylindoles.
Organic letters, 2016, 18, 3330-3333
1543570 CIFC19 H31 N OP 1 21/c 19.3417; 19.5128; 9.2588
90; 99.685; 90		1663.7Kaga, Atsushi; Tnay, Ya Lin; Chiba, Shunsuke
Synthesis of Fasicularin.
Organic letters, 2016, 18, 3506-3508
1543571 CIFC20 H26 N2 O2P -17.5726; 10.186; 12.215
100.996; 93.41; 103.373		894.5Kaga, Atsushi; Tnay, Ya Lin; Chiba, Shunsuke
Synthesis of Fasicularin.
Organic letters, 2016, 18, 3506-3508
1543572 CIFC22 H24 F3 N O3 SP 1 21/n 112.2909; 12.7985; 14.5821
90; 101.076; 90		2251.1Jin, Dong-Po; Gao, Pin; Chen, Dao-Qian; Chen, Si; Wang, Jia; Liu, Xue-Yuan; Liang, Yong-Min
AgSCF3-Mediated Oxidative Trifluoromethythiolation of Alkynes with Dearomatization to Synthesize SCF3-Substituted Spiro[4,5]trienones.
Organic letters, 2016, 18, 3486-3489
1543598 CIFC13 H11 F3 O SP 1 21/c 112.939; 8.252; 11.878
90; 102.167; 90		1239.76Song, Xiaoning; Tian, Shuangquan; Zhao, Ziming; Zhu, Dongsheng; Wang, Mang
Controlled Ring-Opening of Siloxydifluorocyclopropanes for Carbocyclization: Synthesis of Difluorocyclopentenones.
Organic letters, 2016, 18, 3414-3417
1543599 CIFC28 H20 Br Cl N2 O4 S2P 1 21/n 15.4375; 10.0119; 22.541
90; 94.174; 90		1223.9Yu, Junchao; Zhang-Negrerie, Daisy; Du, Yunfei
Cu(OAc)2-Mediated Cascade Annulation of Diarylalkyne Sulfonamides through Dual C-N Bond Formation: Synthesis of 5,10-Dihydroindolo[3,2-b]indoles.
Organic letters, 2016, 18, 3322-3325
1543628 CIFC24 H22 O5 SP -110.091; 10.4061; 11.4027
67.445; 72.988; 70.32		1022.65Xu, Lun; Liu, Fengyi; Xu, Li-Wen; Gao, Ziwei; Zhao, Yu-Ming
A Total Synthesis of Paeoveitol.
Organic letters, 2016, 18, 3698-3701
1543629 CIFC19 H20 O5C 1 2/c 119.3064; 8.9818; 18.1833
90; 95.154; 90		3140.3Xu, Lun; Liu, Fengyi; Xu, Li-Wen; Gao, Ziwei; Zhao, Yu-Ming
A Total Synthesis of Paeoveitol.
Organic letters, 2016, 18, 3698-3701
1543630 CIFC47 H42 Br N3 O6P 21 21 2114.3087; 15.226; 18.5087
90; 90; 90		4032.4Xu, Jianfeng; Yuan, Shiru; Miao, Maozhong
N-Heterocyclic Carbene Catalyzed [4 + 2] Annulation Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes.
Organic letters, 2016, 18, 3822-3825
1543642 CIFC27 H26 N O6P 1 21 17.7825; 33.713; 9.4309
90; 108.491; 90		2346.7Zheng, Kai-Lu; Shu, Wen-Ming; Ma, Jun-Rui; Wu, Yan-Dong; Wu, An-Xin
Acid-Mediated N-H/α,β-C(sp(3))-H Trifunctionalization of Pyrrolidine: Intermolecular [3 + 2] Cycloaddition for the Construction of 2,3-Dihydro-1H-Pyrrolizine Derivatives.
Organic letters, 2016, 18, 3526-3529
1543653 CIFC18 H19 Au Cl N3 O SP 21 21 217.5537; 14.124; 18.002
90; 90; 90		1920.61Frutos, María; Avello, Marta G.; Viso, Alma; Fernández de la Pradilla, Roberto; de la Torre, María C; Sierra, Miguel A.; Gornitzka, Heinz; Hemmert, Catherine
Gold Sulfinyl Mesoionic Carbenes: Synthesis, Structure, and Catalytic Activity.
Organic letters, 2016, 18, 3570-3573
1543654 CIFC18 H19 Au Cl N3 O SP 21 21 2110.9737; 17.4658; 19.9371
90; 90; 90		3821.2Frutos, María; Avello, Marta G.; Viso, Alma; Fernández de la Pradilla, Roberto; de la Torre, María C; Sierra, Miguel A.; Gornitzka, Heinz; Hemmert, Catherine
Gold Sulfinyl Mesoionic Carbenes: Synthesis, Structure, and Catalytic Activity.
Organic letters, 2016, 18, 3570-3573
1543655 CIFC21 H19 Au Cl N3 O2 SP 21 21 217.2343; 11.0385; 26.4489
90; 90; 90		2112.1Frutos, María; Avello, Marta G.; Viso, Alma; Fernández de la Pradilla, Roberto; de la Torre, María C; Sierra, Miguel A.; Gornitzka, Heinz; Hemmert, Catherine
Gold Sulfinyl Mesoionic Carbenes: Synthesis, Structure, and Catalytic Activity.
Organic letters, 2016, 18, 3570-3573
1543668 CIFC38 H42 B2 N2 S2C 1 2/c 121.953; 19.09; 8.7353
90; 108.626; 90		3469.1Zhang, Wanzheng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Zhuang, Xiaodong; He, Gufeng; Feng, Xinliang
Angular BN-Heteroacenes with syn-Structure-Induced Promising Properties as Host Materials of Blue Organic Light-Emitting Diodes.
Organic letters, 2016, 18, 3618-3621
1543669 CIFC30 H22 B2 N2P b c n28.5686; 10.069; 7.7705
90; 90; 90		2235.24Zhang, Wanzheng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Zhuang, Xiaodong; He, Gufeng; Feng, Xinliang
Angular BN-Heteroacenes with syn-Structure-Induced Promising Properties as Host Materials of Blue Organic Light-Emitting Diodes.
Organic letters, 2016, 18, 3618-3621
1543677 CIFC23 H25 Cl2 N3 O4 SP 1 21/n 112.078; 10.4524; 18.2579
90; 93.831; 90		2299.8Dalvi, Prashant B.; Lin, Kuang-Ling; Kulkarni, Manohar V.; Sun, Chung-Ming
Rhodium-Catalyzed Regioselective Synthesis of Isocoumarins through Benzothiadiazine-Fused Frameworks.
Organic letters, 2016, 18, 3706-3709
1543678 CIFC19 H18 Cl N3 O5 SP 1 21/c 110.4885; 12.1708; 14.9547
90; 97.746; 90		1891.6Dalvi, Prashant B.; Lin, Kuang-Ling; Kulkarni, Manohar V.; Sun, Chung-Ming
Rhodium-Catalyzed Regioselective Synthesis of Isocoumarins through Benzothiadiazine-Fused Frameworks.
Organic letters, 2016, 18, 3706-3709
1543679 CIFC32 H25 N3 O5 SP -110.3849; 11.4904; 12.6969
91.474; 97.59; 115.976		1344.14Dalvi, Prashant B.; Lin, Kuang-Ling; Kulkarni, Manohar V.; Sun, Chung-Ming
Rhodium-Catalyzed Regioselective Synthesis of Isocoumarins through Benzothiadiazine-Fused Frameworks.
Organic letters, 2016, 18, 3706-3709
1543680 CIFC19 H18 Cl N3 O5 SP 1 21/n 15.2273; 23.0379; 15.5364
90; 95.558; 90		1862.19Dalvi, Prashant B.; Lin, Kuang-Ling; Kulkarni, Manohar V.; Sun, Chung-Ming
Rhodium-Catalyzed Regioselective Synthesis of Isocoumarins through Benzothiadiazine-Fused Frameworks.
Organic letters, 2016, 18, 3706-3709
1543703 CIFC20 H14 N2 O2P 1 21/n 114.1952; 10.5165; 22.0684
90; 108.529; 90		3123.7Hao, Xin-Qi; Du, Cong; Zhu, Xinju; Li, Peng-Xiang; Zhang, Jia-Heng; Niu, Jun-Long; Song, Mao-Ping
Cobalt(II)-Catalyzed Decarboxylative C-H Activation/Annulation Cascades: Regioselective Access to Isoquinolones and Isoindolinones.
Organic letters, 2016, 18, 3610-3613
1543722 CIFC30 H38 N2 O6 SP 1 21/n 112.6105; 14.074; 17.2452
90; 104.291; 90		2966Potter, Tyler J.; Ellman, Jonathan A.
Rh(III)-Catalyzed C-H Bond Addition/Amine-Mediated Cyclization of Bis-Michael Acceptors.
Organic letters, 2016, 18, 3838-3841
1543735 CIFC26 H18 O2P 1 21/c 110.5123; 6.9425; 26.301
90; 98.712; 90		1897.3Zheng, Min; Wu, Feng; Chen, Kai; Zhu, Shifa
Styrene as 4π-Component in Zn(II)-Catalyzed Intermolecular Diels-Alder/Ene Tandem Reaction.
Organic letters, 2016, 18, 3554-3557
1543749 CIFC29 H44 O3P 1 21 112.1091; 8.3218; 12.7681
90; 93.387; 90		1284.39Liu, Chao; Ang, Song; Huang, Xiao-Jun; Tian, Hai-Yan; Deng, Yuan-Yuan; Zhang, Dong-Mei; Wang, Ying; Ye, Wen-Cai; Wang, Lei
Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K.
Organic letters, 2016, 18, 4004-4007
1543750 CIFC29 H44 O3P 1 21 110.7392; 9.6056; 12.9349
90; 91.623; 90		1333.78Liu, Chao; Ang, Song; Huang, Xiao-Jun; Tian, Hai-Yan; Deng, Yuan-Yuan; Zhang, Dong-Mei; Wang, Ying; Ye, Wen-Cai; Wang, Lei
Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K.
Organic letters, 2016, 18, 4004-4007
1543751 CIFC29 H44 O3P 21 21 218.35689; 16.2511; 19.1684
90; 90; 90		2603.23Liu, Chao; Ang, Song; Huang, Xiao-Jun; Tian, Hai-Yan; Deng, Yuan-Yuan; Zhang, Dong-Mei; Wang, Ying; Ye, Wen-Cai; Wang, Lei
Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K.
Organic letters, 2016, 18, 4004-4007
1543765 CIFC20 H21 N3P 1 21 17.1149; 26.5631; 8.515
90; 90.955; 90		1609.06Suh, Sung-Eun; Chenoweth, David M.
Aryne Compatible Solvents are not Always Innocent.
Organic letters, 2016, 18, 4080-4083
1543766 CIFC19 H20 Cl2 N2P 21 21 218.5618; 8.6657; 22.783
90; 90; 90		1690.4Suh, Sung-Eun; Chenoweth, David M.
Aryne Compatible Solvents are not Always Innocent.
Organic letters, 2016, 18, 4080-4083
1543767 CIFC21 H14 N2 O2 SP 1 21/c 113.5638; 6.3615; 20.0924
90; 101.767; 90		1697.26Kalogirou, Andreas S.; Kourtellaris, Andreas; Koutentis, Panayiotis A.
The Acid and/or Thermal Mediated Ring Contraction of 4H-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazoles.
Organic letters, 2016, 18, 4056-4059
1543768 CIFC21 H12 N4 O6 SP 1 21 17.9088; 13.4071; 9.205
90; 93.738; 90		973.97Kalogirou, Andreas S.; Kourtellaris, Andreas; Koutentis, Panayiotis A.
The Acid and/or Thermal Mediated Ring Contraction of 4H-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazoles.
Organic letters, 2016, 18, 4056-4059
1543769 CIFC22 H15 N3 O5 SP 1 21/c 17.5707; 6.8326; 37.456
90; 94.606; 90		1931.3Kalogirou, Andreas S.; Kourtellaris, Andreas; Koutentis, Panayiotis A.
The Acid and/or Thermal Mediated Ring Contraction of 4H-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazoles.
Organic letters, 2016, 18, 4056-4059
1543779 CIFC15 H16 N2 O4 SP -19.9165; 12.3529; 13.2009
106.393; 94.388; 95.96		1533.4Seitz, Tobias; Fu, Peng; Haut, Franz-Lucas; Adam, Lutz; Habicht, Marija; Lentz, Dieter; MacMillan, John B.; Christmann, Mathias
One-Pot Synthesis of 5-Hydroxy-4H-1,3-thiazin-4-ones: Structure Revision, Synthesis, and NMR Shift Dependence of Thiasporine A.
Organic letters, 2016, 18, 3070-3073
1543780 CIFC16 H17 N2 O1.5C 1 2/c 112.441; 8.216; 26.04
90; 93.756; 90		2656Hati, Santanu; Kumar Dutta, Pratip; Dutta, Sanjay; Munshi, Parthapratim; Sen, Subhabrata
Accessing Benzimidazoles via a Ring Distortion Strategy: An Oxone Mediated Tandem Reaction of 2-Aminobenzylamines.
Organic letters, 2016, 18, 3090-3093
1543781 CIFC23 H19 Cl2 N O3C 1 2/c 132.758; 9.5956; 14.9338
90; 116.53; 90		4199.9Zhang, Tian-Shu; Hao, Wen-Juan; Wang, Nan-Nan; Li, Guigen; Jiang, Dong-Fang; Tu, Shu-Jiang; Jiang, Bo
Catalytic Oxidative Carbene Coupling of α-Diazo Carbonyls for the Synthesis of β-Amino Ketones via C(sp(3))-H Functionalization.
Organic letters, 2016, 18, 3078-3081
1543782 CIFC20 H40 Cl N5 Ni O2 P2P 1 21/n 117.951; 14.649; 22.079
90; 113.927; 90		5307Mastalir, Matthias; Stöger, Berthold; Pittenauer, Ernst; Allmaier, Günter; Kirchner, Karl
Air-Stable Triazine-Based Ni(II) PNP Pincer Complexes As Catalysts for the Suzuki-Miyaura Cross-Coupling.
Organic letters, 2016, 18, 3186-3189
1543783 CIFC17 H36 Cl2 N6 Ni P2P b c n18.1927; 14.0509; 21.446
90; 90; 90		5482.1Mastalir, Matthias; Stöger, Berthold; Pittenauer, Ernst; Allmaier, Günter; Kirchner, Karl
Air-Stable Triazine-Based Ni(II) PNP Pincer Complexes As Catalysts for the Suzuki-Miyaura Cross-Coupling.
Organic letters, 2016, 18, 3186-3189
1543784 CIFC20 H14 F6 N2 O4 S2P -19.2794; 11.1179; 12.038
84.916; 69.397; 79.875		1143.91Qiu, Dachuan; He, Jia; Yue, Xiao; Shi, Jiarong; Li, Yang
Diamination of Domino Aryne Precursor with Sulfonamides.
Organic letters, 2016, 18, 3130-3133
1543785 CIFC50 H22 O2P 1 21/n 111.0215; 13.1109; 15.1972
90; 111.193; 90		2047.5Kumarasinghe, K G Upul R; Fronczek, Frank R.; Valle, Henry U.; Sygula, Andrzej
Bis-corannulenoanthracene: An Angularly Fused Pentacene as a Precursor for Barrelene-Tethered Receptors for Fullerenes.
Organic letters, 2016, 18, 3054-3057
1543786 CIFC61 H32 O3P 1 21/m 110.889; 13.3104; 13.9583
90; 106.526; 90		1939.5Kumarasinghe, K G Upul R; Fronczek, Frank R.; Valle, Henry U.; Sygula, Andrzej
Bis-corannulenoanthracene: An Angularly Fused Pentacene as a Precursor for Barrelene-Tethered Receptors for Fullerenes.
Organic letters, 2016, 18, 3054-3057
1543787 CIFC26.25 H28.5 Cl0.5 F7 N3 O SC 1 2 119.7969; 12.4055; 14.0366
90; 122.117; 90		2919.7Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543788 CIFC16 H22 F N O2P 21 21 216.3738; 10.3067; 22.7482
90; 90; 90		1494.39Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543789 CIFC29 H36 F6 N3 O SC 1 2 119.631; 12.4696; 14.2862
90; 122.586; 90		2946.6Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543790 CIFC56.5 H68.5 Cl2.5 F14 N7 O4P 21 21 2114.092; 18.525; 46.955
90; 90; 90		12258Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543791 CIFC56 H68 Cl F14 N7 O2 S2P 19.7657; 12.7259; 26.975
86.183; 83.556; 70.327		3135.3Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543792 CIFC31 H41 Cl4 F7 N4 O2P 21 21 219.2304; 13.9651; 28.899
90; 90; 90		3725.2Lehnherr, Dan; Ford, David D.; Bendelsmith, Andrew J.; Kennedy, C. Rose; Jacobsen, Eric N.
Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity.
Organic letters, 2016, 18, 3214-3217
1543793 CIFC20 H14 N2 O S SeP 1 21/c 115.14; 7.9011; 14.1502
90; 91.3074; 90		1692.24Mandal, Anup; Sahoo, Harekrishna; Baidya, Mahiuddin
Copper-Catalyzed 8-Aminoquinoline-Directed Selenylation of Arene and Heteroarene C-H Bonds.
Organic letters, 2016, 18, 3202-3205
1543794 CIFC27 H19 Cl2 N3 O2 Se2P -17.5562; 13.4128; 14.1944
64.824; 85.1858; 88.7061		1297.21Mandal, Anup; Sahoo, Harekrishna; Baidya, Mahiuddin
Copper-Catalyzed 8-Aminoquinoline-Directed Selenylation of Arene and Heteroarene C-H Bonds.
Organic letters, 2016, 18, 3202-3205
1543795 CIFC20 H14 N2 O3 S SeP 1 21/c 114.7324; 8.1294; 15.0674
90; 91.7272; 90		1803.74Mandal, Anup; Sahoo, Harekrishna; Baidya, Mahiuddin
Copper-Catalyzed 8-Aminoquinoline-Directed Selenylation of Arene and Heteroarene C-H Bonds.
Organic letters, 2016, 18, 3202-3205
1543796 CIFC12 H18 O2P 21 21 216.431; 8.943; 18.239
90; 90; 90		1049Barthel, André; Kaden, Felix; Jäger, Anne; Metz, Peter
Enantioselective Synthesis of Guaianolides in the Osmitopsin Family by Domino Metathesis.
Organic letters, 2016, 18, 3298-3301
1543797 CIFC14 H20 O3P 21 21 216.223; 7.076; 28.09
90; 90; 90		1236.9Barthel, André; Kaden, Felix; Jäger, Anne; Metz, Peter
Enantioselective Synthesis of Guaianolides in the Osmitopsin Family by Domino Metathesis.
Organic letters, 2016, 18, 3298-3301
1543798 CIFC14 H20 O3P 1 21 110.523; 9.378; 12.89
90; 91.59; 90		1271.6Barthel, André; Kaden, Felix; Jäger, Anne; Metz, Peter
Enantioselective Synthesis of Guaianolides in the Osmitopsin Family by Domino Metathesis.
Organic letters, 2016, 18, 3298-3301
1543799 CIFC26 H28 N4 O6C 1 2 121.15; 4.978; 24.55
90; 104.86; 90		2498Kashinath, K.; Jachak, Gorakhnath R.; Athawale, Paresh R.; Marelli, Udaya Kiran; Gonnade, Rajesh G.; Reddy, D. Srinivasa
Total Synthesis of the Marine Natural Product Solomonamide B Necessitates Stereochemical Revision.
Organic letters, 2016, 18, 3178-3181
1543800 CIFC30 H38 N4 O7C 1 2 128.205; 5.7857; 17.974
90; 91.077; 90		2932.6Kashinath, K.; Jachak, Gorakhnath R.; Athawale, Paresh R.; Marelli, Udaya Kiran; Gonnade, Rajesh G.; Reddy, D. Srinivasa
Total Synthesis of the Marine Natural Product Solomonamide B Necessitates Stereochemical Revision.
Organic letters, 2016, 18, 3178-3181
1543801 CIFC24 H21 Br N2 O2 SP -19.0001; 9.6916; 13.9766
90.203; 105.459; 116.432		1041.58Shu, Chao; Wang, Yong-Heng; Shen, Cang-Hai; Ruan, Peng-Peng; Lu, Xin; Ye, Long-Wu
Gold-Catalyzed Intermolecular Ynamide Amination-Initiated Aza-Nazarov Cyclization: Access to Functionalized 2-Aminopyrroles.
Organic letters, 2016, 18, 3254-3257
1543802 CIFC15 H13 Br O6P 1 21/c 114.5589; 5.345; 18.6931
90; 98.725; 90		1437.81Alamillo-Ferrer, Carla; Karabourniotis-Sotti, Marianna; Kennedy, Alan R.; Campbell, Matthew; Tomkinson, Nicholas C. O.
Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans.
Organic letters, 2016, 18, 3102-3105
1543803 CIFC14 H12 O6P -17.9639; 8.2187; 9.601
92.174; 109.731; 92.209		590.21Alamillo-Ferrer, Carla; Karabourniotis-Sotti, Marianna; Kennedy, Alan R.; Campbell, Matthew; Tomkinson, Nicholas C. O.
Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans.
Organic letters, 2016, 18, 3102-3105
1543804 CIFC17 H20 O5P 1 21/c 110.6142; 6.9676; 21.0046
90; 97.064; 90		1541.61Alamillo-Ferrer, Carla; Karabourniotis-Sotti, Marianna; Kennedy, Alan R.; Campbell, Matthew; Tomkinson, Nicholas C. O.
Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans.
Organic letters, 2016, 18, 3102-3105
1543805 CIFC30 H23 N O4 SP n a 2118.3425; 10.4967; 52.3489
90; 90; 90		10079Prabagar, B.; Nayak, Sanatan; Prasad, Rangu; Sahoo, Akhila K.
Dimethyl Sulfoxide and N-Iodosuccinimide Promoted 5-exo-dig Oxidative Cyclization of Yne-Tethered Ynamide: Access to Pyrrolidones and Spiro-pyrrolidones.
Organic letters, 2016, 18, 3066-3069
1543806 CIFC23 H17 N O2P n a 2111.9577; 33.256; 8.9182
90; 90; 90		3546.5Prabagar, B.; Nayak, Sanatan; Prasad, Rangu; Sahoo, Akhila K.
Dimethyl Sulfoxide and N-Iodosuccinimide Promoted 5-exo-dig Oxidative Cyclization of Yne-Tethered Ynamide: Access to Pyrrolidones and Spiro-pyrrolidones.
Organic letters, 2016, 18, 3066-3069
1543807 CIFC21 H19 Br O2P 1 21 111.911; 5.8447; 12.531
90; 103.47; 90		848.4Ahlin, Joachim S. E.; Cramer, Nicolai
Chiral N-Heterocyclic Carbene Ligand Enabled Nickel(0)-Catalyzed Enantioselective Three-Component Couplings as Direct Access to Silylated Indanols.
Organic letters, 2016, 18, 3242-3245
1543808 CIFC18 H15 Cl4 N O3P -17.9118; 11.5272; 11.8921
68.353; 88.982; 82.872		999.83Bai, Peng; Huang, Xing-Fen; Xu, Guo-Dong; Huang, Zhi-Zhen
Cascade C-H Functionalization/Amidation Reaction for Synthesis of Azepinone Derivatives.
Organic letters, 2016, 18, 3058-3061
1543809 CIFC40 H42 O2 S8P b c n4.4192; 33.029; 27.3541
90; 90; 90		3992.7Khadem, Mohammadreza; Walsh, Joshua C.; Bodwell, Graham J.; Zhao, Yuming
A Macrocyclization of 1,8-Bis(dithiafulvenyl)pyrenes.
Organic letters, 2016, 18, 2403-2406
1543810 CIFC16 H11 N O2P n a 2117.8024; 7.7552; 17.7401
90; 90; 90		2449.2Chen, Xiaopei; Cui, Xiuling; Wu, Yangjie
"One-Pot" Approach to 8-Acylated 2-Quinolinones via Palladium-Catalyzed Regioselective Acylation of Quinoline N-Oxides.
Organic letters, 2016, 18, 2411-2414
1543811 CIFC16 H11 N O2P n a 217.0519; 23.5069; 7.5339
90; 90; 90		1248.88Chen, Xiaopei; Cui, Xiuling; Wu, Yangjie
"One-Pot" Approach to 8-Acylated 2-Quinolinones via Palladium-Catalyzed Regioselective Acylation of Quinoline N-Oxides.
Organic letters, 2016, 18, 2411-2414
1543812 CIFC28 H23 Cl3 N O P PdP 1 21/n 110.2608; 16.6441; 15.6634
90; 92.089; 90		2673.2Chen, Xiaopei; Cui, Xiuling; Wu, Yangjie
"One-Pot" Approach to 8-Acylated 2-Quinolinones via Palladium-Catalyzed Regioselective Acylation of Quinoline N-Oxides.
Organic letters, 2016, 18, 2411-2414
1543813 CIFC31 H29 N2P -110.116; 10.554; 11.501
105.31; 93.11; 96.37		1172.5Wang, Hongkai; Wang, Chan; Huang, Kaimeng; Liu, Lingyan; Chang, Weixing; Li, Jing
Copper-Catalyzed Cascade Reaction via Intramolecular Hydroamination Cyclization of Homopropargylic Amines and Intermolecular Povarov Reaction with Imines.
Organic letters, 2016, 18, 2367-2370
1543814 CIFC23 H26 Cl N O3 SP 1 21 18.1254; 14.0815; 10.0099
90; 110.328; 90		1073.98Yeh, Ming-Chang P; Shiue, Yuan-Shin; Lin, Hsin-Hui; Yu, Tzu-Yu; Hu, Ting-Chia; Hong, Jia-Jyun
Iron(II) Halide Promoted Cyclization of Cyclic 2-Enynamides: Stereoselective Synthesis of Halogenated Bicyclic γ-Lactams.
Organic letters, 2016, 18, 2407-2410
1543815 CIFC19 H20 Cl N O3 S2C 1 2/c 112.314; 16.902; 19.984
90; 107.769; 90		3961Yeh, Ming-Chang P; Shiue, Yuan-Shin; Lin, Hsin-Hui; Yu, Tzu-Yu; Hu, Ting-Chia; Hong, Jia-Jyun
Iron(II) Halide Promoted Cyclization of Cyclic 2-Enynamides: Stereoselective Synthesis of Halogenated Bicyclic γ-Lactams.
Organic letters, 2016, 18, 2407-2410
1543816 CIFC24 H28 Cl N O3 SP -111.767; 12.4537; 15.7544
80.281; 88.759; 84.902		2266.5Yeh, Ming-Chang P; Shiue, Yuan-Shin; Lin, Hsin-Hui; Yu, Tzu-Yu; Hu, Ting-Chia; Hong, Jia-Jyun
Iron(II) Halide Promoted Cyclization of Cyclic 2-Enynamides: Stereoselective Synthesis of Halogenated Bicyclic γ-Lactams.
Organic letters, 2016, 18, 2407-2410
1543817 CIFC21 H22 Br N O3 SP n a 2123.544; 6.96; 24.234
90; 90; 90		3971.1Yeh, Ming-Chang P; Shiue, Yuan-Shin; Lin, Hsin-Hui; Yu, Tzu-Yu; Hu, Ting-Chia; Hong, Jia-Jyun
Iron(II) Halide Promoted Cyclization of Cyclic 2-Enynamides: Stereoselective Synthesis of Halogenated Bicyclic γ-Lactams.
Organic letters, 2016, 18, 2407-2410
1543818 CIFC38 H48 O6 SiP -111.2348; 11.3819; 14.1336
87.511; 81.82; 82.982		1774.9Zhou, Jia-Hui; Cai, Sai-Hu; Xu, Yun-He; Loh, Teck-Peng
Anomalous Reactivity and Selectivity in the Intermolecular Diels-Alder Reactions of Multisubstituted Acyclic Dienes with Geometrical Isomers of Enals.
Organic letters, 2016, 18, 2355-2358
1543819 CIFC30 H39 N3 O10 SP -112.1373; 12.1458; 12.5058
95.4973; 105.159; 113.259		1593.08Yamaguchi, Mami; Hayashi, Minami; Hamada, Yasumasa; Nemoto, Tetsuhiro
Synthetic Study of Pactamycin: Enantioselective Construction of the Pactamycin Core with Five Contiguous Stereocenters.
Organic letters, 2016, 18, 2347-2350
1543820 CIFC18 H17 NF d d 230.399; 12.677; 14.356
90; 90; 90		5532Zhou, Shuguang; Wang, Jinhu; Zhang, Feifei; Song, Chao; Zhu, Jin
A Versatile, Traceless C-H Activation-Based Approach for the Synthesis of Heterocycles.
Organic letters, 2016, 18, 2427-2430
1543821 CIFC12 H15 N O3P 1 21/c 114.736; 5.881; 14.065
90; 107.9; 90		1159.9Zhou, Shuguang; Wang, Jinhu; Zhang, Feifei; Song, Chao; Zhu, Jin
A Versatile, Traceless C-H Activation-Based Approach for the Synthesis of Heterocycles.
Organic letters, 2016, 18, 2427-2430
1543822 CIFC16 H15 NP 1 21/n 112.08; 8.276; 12.564
90; 90.03; 90		1256.1Zhou, Shuguang; Wang, Jinhu; Zhang, Feifei; Song, Chao; Zhu, Jin
A Versatile, Traceless C-H Activation-Based Approach for the Synthesis of Heterocycles.
Organic letters, 2016, 18, 2427-2430
1543823 CIFC17 H22 Cl N2 RhP -18.3882; 14.1471; 14.5826
84.405; 81.153; 84.229		1695.31Zhou, Shuguang; Wang, Jinhu; Zhang, Feifei; Song, Chao; Zhu, Jin
A Versatile, Traceless C-H Activation-Based Approach for the Synthesis of Heterocycles.
Organic letters, 2016, 18, 2427-2430
1543824 CIFC14 H9 Br I N O2P 1 21/n 18.4169; 13.403; 13.054
90; 107.974; 90		1400.8Wu, Xia; Gao, Qinghe; Geng, Xiao; Zhang, Jingjing; Wu, Yan-Dong; Wu, An-Xin
Iodine-Promoted Oxidative Cross-Coupling of Unprotected Anilines with Methyl Ketones: A Site-Selective Direct C-H Bond Functionalization to C4-Dicarbonylation of Anilines.
Organic letters, 2016, 18, 2507-2510
1543825 CIFC19 H22 N2 O2P -17.1942; 10.7514; 13.461
106.944; 95.85; 98.867		972.1Zhao, Gaoyuan; Xie, Xingang; Sun, Haiyu; Yuan, Ziyun; Zhong, Zhuliang; Tang, Shouchu; She, Xuegong
Bioinspired Collective Syntheses of Iboga-Type Indole Alkaloids.
Organic letters, 2016, 18, 2447-2450
1543826 CIFC14 H18 N O5 PP -18.0151; 9.9592; 10.3467
69.516; 72.945; 89.454		735.66Phatake, Ravindra S.; Patel, Pitambar; Ramana, Chepuri V.
Ir(III)-Catalyzed Carbenoid Functionalization of Benzamides: Synthesis of N-Methoxyisoquinolinediones and N-Methoxyisoquinolinones.
Organic letters, 2016, 18, 2828-2831
1543827 CIFC10 H8 Cl N O3P 1 21/c 19.2286; 12.6651; 8.3177
90; 96.24; 90		966.42Phatake, Ravindra S.; Patel, Pitambar; Ramana, Chepuri V.
Ir(III)-Catalyzed Carbenoid Functionalization of Benzamides: Synthesis of N-Methoxyisoquinolinediones and N-Methoxyisoquinolinones.
Organic letters, 2016, 18, 2828-2831
1543828 CIFC26 H22 N2 O2P c a 2119.3078; 10.3786; 20.7335
90; 90; 90		4154.7Zhang, Jianbo; Han, Xiuling; Lu, Xiyan
Synthesis of Indole-Substituted Indanones via Palladium(II)-Catalyzed Tandem Reaction of ortho-Electron-Deficient Alkynyl-Substituted Aryl Aldehydes with Indoles.
Organic letters, 2016, 18, 2898-2901
1543829 CIFC26 H32 O5P 17.2748; 12.323; 13.1676
114.212; 90.277; 91.395		1076.14Liu, Cui-Ping; Wang, Guo-Cai; Gan, Li-She; Xu, Cheng-Hui; Liu, Qun-Fang; Ding, Jian; Yue, Jian-Min
Ciliatonoids A and B, Two Limonoids from Toona ciliata.
Organic letters, 2016, 18, 2894-2897
1543830 CIFC30 H22 F3 N O2P -18.959; 10.483; 13.867
77.615; 85.443; 71.589		1206.8He, Ke-Han; Zhang, Wei-Dong; Yang, Ming-Yu; Tang, Kai-Li; Qu, Mengnan; Ding, You-Song; Li, Yang
Redox-Divergent Hydrogen-Retentive or Hydrogen-Releasing Synthesis of 3,4-Dihydroisoquinolines or Isoquinolines.
Organic letters, 2016, 18, 2840-2843
1543831 CIFC36 H24 Cl4 N O0P -19.2698; 12.7098; 14.3453
74.173; 75.883; 79.171		1563.5He, Ke-Han; Zhang, Wei-Dong; Yang, Ming-Yu; Tang, Kai-Li; Qu, Mengnan; Ding, You-Song; Li, Yang
Redox-Divergent Hydrogen-Retentive or Hydrogen-Releasing Synthesis of 3,4-Dihydroisoquinolines or Isoquinolines.
Organic letters, 2016, 18, 2840-2843
1543832 CIFC31 H37 O SiC 1 2/c 136.1249; 17.0168; 8.3417
90; 93.726; 90		5117.1Yadav, Priya; Das, Soumyajit; Phan, Hoa; Herng, Tun Seng; Ding, Jun; Wu, Jishan
Kinetically Blocked Stable 5,6:12,13-Dibenzozethrene: A Laterally π-Extended Zethrene with Enhanced Diradical Character.
Organic letters, 2016, 18, 2886-2889
1543833 CIFC39 H42 O18C 1 2/c 139.372; 8.0823; 27.4716
90; 121.374; 90		7463.7Xia, Danyu; Li, Yang; Jie, Kecheng; Shi, Bingbing; Yao, Yong
A Water-Soluble Cyclotriveratrylene-Based Supra-amphiphile: Synthesis, pH-Responsive Self-Assembly in Water, and Its Application in Controlled Drug Release.
Organic letters, 2016, 18, 2910-2913
1543834 CIFC46 H14 F20 N4P 4/n c c20.2347; 20.2347; 9.6664
90; 90; 90		3957.8Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543835 CIFC31 H11 F15 N2 O2P 1 21/c 129.637; 11.513; 36.067
90; 116.512; 90		11012Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543836 CIFC17 H13 F5 N2P 21 21 216.934; 11.235; 19.486
90; 90; 90		1518Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543837 CIFC31 H11 F15 N2 O2P 1 21/n 110.44; 21.459; 13.031
90; 107.973; 90		2776.9Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543838 CIFC39 H15 F15 N4F d d 229.84; 85.63; 5.44
90; 90; 90		13900Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543839 CIFC45.2 H30.81 F12 N4 O3.2P 1 21/a 111.642; 30.056; 11.989
90; 105.322; 90		4046Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543840 CIFC47.5 H17 Cl3 F20 N4 OP -110.2204; 14.8005; 15.9075
65.355; 88.006; 86.758		2183.4Naito, Wakana; Yasuda, Nobuhiro; Morimoto, Tatsuki; Shigeta, Yasuteru; Takaya, Hikaru; Hisaki, Ichiro; Maeda, Hiromitsu
Doubly N-Methylated Porphyrinoids.
Organic letters, 2016, 18, 3006-3009
1543841 CIFC18 H15 Br N2 OP -18.184; 9.7886; 10.6117
107.346; 97.071; 111.202		730.6Wang, He; Li, Lei; Yu, Songjie; Li, Yunyun; Li, Xingwei
Rh(III)-Catalyzed C-C/C-N Coupling of Imidates with α-Diazo Imidamide: Synthesis of Isoquinoline-Fused Indoles.
Organic letters, 2016, 18, 2914-2917
1543842 CIFC45 H45 N5 O2 ZnP 1 21/c 119.5138; 7.8297; 25.5113
90; 105.181; 90		3761.77Omori, Hiroto; Hiroto, Satoru; Shinokubo, Hiroshi
Synthesis of Free-Base 10-Azacorroles.
Organic letters, 2016, 18, 2978-2981
1543843 CIFC45 H40.84 Br0.16 Cl2 N5 PdP 1 21/c 116.4227; 20.557; 12.5961
90; 112.282; 90		3934.9Omori, Hiroto; Hiroto, Satoru; Shinokubo, Hiroshi
Synthesis of Free-Base 10-Azacorroles.
Organic letters, 2016, 18, 2978-2981
1543844 CIFC19 H17 Br N2 O4P 21 21 217.3051; 11.626; 20.629
90; 90; 90		1752Cayuelas, Alberto; Ortiz, Ricardo; Nájera, Carmen; Sansano, José M; Larrañaga, Olatz; de Cózar, Abel; Cossío, Fernando P
Enantioselective Synthesis of Polysubstituted Spiro-nitroprolinates Mediated by a (R,R)-Me-DuPhos·AgF-Catalyzed 1,3-Dipolar Cycloaddition.
Organic letters, 2016, 18, 2926-2929
1543852 CIFC16 H13 Cl O3P 21 21 2111.829; 12.023; 19.877
90; 90; 90		2826.9Wen, Genfa; Su, Yingpeng; Zhang, Guoxiang; Lin, Qiqiao; Zhu, Yujin; Zhang, Qianqian; Fang, Xinqiang
Stereodivergent Synthesis of Chromanones and Flavanones via Intramolecular Benzoin Reaction.
Organic letters, 2016, 18, 3980-3983
1543936 CIFC11 H11 Cl F3 N5P 1 21/c 14.737; 17.24; 16.17
90; 96.201; 90		1312.8Guo, Ran; Zheng, Yan; Ma, Jun-An
Electrophilic Reaction of 2,2,2-Trifluorodiazoethane with the in Situ Generated N-Heterocyclic Carbenes: Access to N-Aminoguanidines.
Organic letters, 2016, 18, 4170-4173
1543937 CIFC23 H25 F3 N4P 1 21/c 18.1397; 21.9119; 12.7475
90; 95.889; 90		2261.6Guo, Ran; Zheng, Yan; Ma, Jun-An
Electrophilic Reaction of 2,2,2-Trifluorodiazoethane with the in Situ Generated N-Heterocyclic Carbenes: Access to N-Aminoguanidines.
Organic letters, 2016, 18, 4170-4173
1543938 CIFC32 H27 F3 N6 O2 SP 1 21 19.6443; 11.0756; 28.466
90; 94.032; 90		3033.1Guo, Ran; Zheng, Yan; Ma, Jun-An
Electrophilic Reaction of 2,2,2-Trifluorodiazoethane with the in Situ Generated N-Heterocyclic Carbenes: Access to N-Aminoguanidines.
Organic letters, 2016, 18, 4170-4173
1543939 CIFC23 H29 F O2P -16.027; 8.625; 20.271
80.818; 84.718; 80.883		1024.7Dai, Wenpeng; Shi, Hongyan; Zhao, Xianghu; Cao, Song
Sterically Controlled Cu-Catalyzed or Transition-Metal-Free Cross-Coupling of gem-Difluoroalkenes with Tertiary, Secondary, and Primary Alkyl Grignard Reagents.
Organic letters, 2016, 18, 4284-4287
1543962 CIFC17 H23 N4 O6 PP 21 21 219.73106; 10.22183; 19.6704
90; 90; 90		1956.6Chen, Jing; Wen, Xiaojing; Wang, Yan; Du, Fei; Cai, Liu; Peng, Yungui
Asymmetric Mannich Reaction of Isatin-Based Ketimines with α-Diazomethylphosphonates Catalyzed by Chiral Silver Phosphate.
Organic letters, 2016, 18, 4336-4339
1543963 CIFC18 H11 N SP 1 21/c 16.9955; 14.118; 12.822
90; 98.536; 90		1252.3Hagui, Wided; Besbes, Néji; Srasra, Ezzeddine; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri
Short Synthesis of Sulfur Analogues of Polyaromatic Hydrocarbons through Three Palladium-Catalyzed C-H Bond Arylations.
Organic letters, 2016, 18, 4182-4185
1543990 CIFC19 H22 Br N O2C 1 2/c 118.966; 12.681; 16.462
90; 116.614; 90		3539.7Cheng, Jie; Deng, Xia; Wang, Guoqiang; Li, Ying; Cheng, Xu; Li, Guigen
Intermolecular C-H Quaternary Alkylation of Aniline Derivatives Induced by Visible-Light Photoredox Catalysis.
Organic letters, 2016, 18, 4538-4541
1543991 CIFC44 H28 O4P b c n7.9399; 20.8101; 19.6719
90; 90; 90		3250.4Zhu, Hai-Tao; Ke, Sen; Zhou, Ni-Ni; Fan, Ming-Jin; Yang, De-Suo
Regioselective Intermolecular [2 + 2]-Cycloaddition of α-Iodo-Unsaturated Ketones Promoted by Diisobutylaluminum Hydride.
Organic letters, 2016, 18, 4554-4557
1544024 CIFC20 H21 N3 O4 SP -19.4679; 10.2537; 10.3314
95.058; 91.227; 99.386		985.05Zhang, Ziqian; Li, Yi; He, Haihong; Qian, Xuhong; Yang, Youjun
Mild Chemotriggered Generation of a Fluorophore-Tethered Diazoalkane Species via Smiles Rearrangement.
Organic letters, 2016, 18, 4674-4677
1544033 CIFC27 H22 Cl N3 O2C 1 2/c 122.5227; 13.0043; 16.6637
90; 105.449; 90		4704.3Zhou, Xiaorong; Fan, Zili; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization.
Organic letters, 2016, 18, 4706-4709
1544034 CIFC27 H17 Cl N4 OP 1 21/n 17.9757; 11.0702; 25.2461
90; 90.966; 90		2228.73Zhou, Xiaorong; Fan, Zili; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization.
Organic letters, 2016, 18, 4706-4709
1544036 CIFC34 H29 N O4P 21 21 219.6012; 14.683; 38.686
90; 90; 90		5453.7Han, Dandan; Chen, Jinjin; He, Qiuqin; Fan, Renhua
Dearomatization-Induced Cycloaddition and Aromatization-Triggered Rearrangement: Synthesis of Vertically Expanded Five-Ring Fused Benzofurans.
Organic letters, 2016, 18, 4690-4693
1544066 CIFC19 H22 Br N O4P 21 21 218.5367; 15.0339; 14.7258
90; 90; 90		1889.9Zhou, Fengtao; Yamamoto, Hisashi
A Disulfonimide Catalyst for Highly Enantioselective Mukaiyama-Mannich Reaction.
Organic letters, 2016, 18, 4974-4977
1544067 CIFC16 H20 N6P 1 21/a 112.3916; 9.7149; 13.2453
90; 94.592; 90		1589.39Kroon, Edwin; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
Cleavable β-Cyanoethyl Isocyanide in the Ugi Tetrazole Reaction.
Organic letters, 2016, 18, 4762-4765
1544143 CIFC24 H21 N OP 1 21 18.9816; 29.4224; 13.9309
90; 90.128; 90		3681.4Yamamoto, Kosuke; Qureshi, Zafar; Tsoung, Jennifer; Pisella, Guillaume; Lautens, Mark
Combining Ru-Catalyzed C-H Functionalization with Pd-Catalyzed Asymmetric Allylic Alkylation: Synthesis of 3-Allyl-3-aryl Oxindole Derivatives from Aryl α-Diazoamides.
Organic letters, 2016, 18, 4954-4957
1544163 CIFC16 H18 O6P c a 2111.97; 16; 8.19
90; 90; 90		1568.5Ren, Zhiqiang; Hao, Yu; Hu, Xiangdong
Total Synthesis and Structural Reassignment of (±)-Cereoanhydride.
Organic letters, 2016, 18, 4958-4961
1544164 CIFC32 H38 B N3 OP 1 21/n 117.022; 8.362; 19.77
90; 95.585; 90		2801Nishikawa, Daiki; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Regio- and Stereoselective Aminoboration of Alkenylboronates.
Organic letters, 2016, 18, 4856-4859
1544165 CIFC32 H39 B2 N5 OP 1 21/c 111.904; 10.2654; 23.98
90; 100.941; 90		2877Nishikawa, Daiki; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Regio- and Stereoselective Aminoboration of Alkenylboronates.
Organic letters, 2016, 18, 4856-4859
1544166 CIFC32 H38 O3P 1 21/n 110.361; 25.338; 11.4215
90; 114.89; 90		2719.9Huang, Bo; Shen, Yangyong; Mao, Zhenjun; Liu, Yu; Cui, Sunliang
Metathesis Reaction of Diazo Compounds and para-Quinone Methides for C-C Double Bond Formation: Synthesis of Tetrasubstituted Alkenes and Quinolinones.
Organic letters, 2016, 18, 4888-4891
1544167 CIFC22 H16 Cl N O2P 1 21/n 113.002; 10.771; 13.596
90; 109.47; 90		1795.2Huang, Bo; Shen, Yangyong; Mao, Zhenjun; Liu, Yu; Cui, Sunliang
Metathesis Reaction of Diazo Compounds and para-Quinone Methides for C-C Double Bond Formation: Synthesis of Tetrasubstituted Alkenes and Quinolinones.
Organic letters, 2016, 18, 4888-4891
1544168 CIFC30 H34 N0 O3P 1 21/c 110.472; 26.208; 11.754
90; 100.641; 90		3170Huang, Bo; Shen, Yangyong; Mao, Zhenjun; Liu, Yu; Cui, Sunliang
Metathesis Reaction of Diazo Compounds and para-Quinone Methides for C-C Double Bond Formation: Synthesis of Tetrasubstituted Alkenes and Quinolinones.
Organic letters, 2016, 18, 4888-4891
1544169 CIFC31 H36 O3P -19.6348; 11.1945; 13.2323
107.248; 100.253; 93.543		1331.24Huang, Bo; Shen, Yangyong; Mao, Zhenjun; Liu, Yu; Cui, Sunliang
Metathesis Reaction of Diazo Compounds and para-Quinone Methides for C-C Double Bond Formation: Synthesis of Tetrasubstituted Alkenes and Quinolinones.
Organic letters, 2016, 18, 4888-4891
1544170 CIFC30 H34 Cl N O2P 1 21/c 114.1486; 11.072; 17.2118
90; 92.697; 90		2693.3Huang, Bo; Shen, Yangyong; Mao, Zhenjun; Liu, Yu; Cui, Sunliang
Metathesis Reaction of Diazo Compounds and para-Quinone Methides for C-C Double Bond Formation: Synthesis of Tetrasubstituted Alkenes and Quinolinones.
Organic letters, 2016, 18, 4888-4891
1544189 CIFC24 H27 Br N2 O2P b c a13.636; 10.254; 30.557
90; 90; 90		4272.6Lu, Kui; Ma, Yantao; Gao, Meile; Liu, Yan; Li, Ming; Xu, Chuanming; Zhao, Xia; Yu, Peng
1,4-Addition Ugi Reaction Using Cyclic α,β-Unsaturated Ketone as Substrate.
Organic letters, 2016, 18, 5038-5041
1544222 CIFC25 H17 Cl N O PP 1 21/c 113.831; 16.046; 9.43
90; 105.784; 90		2013.9Li, Chun-Xiao; Tu, De-Shuang; Yao, Rui; Yan, Hong; Lu, Chang-Sheng
Visible-Light-Induced Cascade Reaction of Isocyanides and N-Arylacrylamides with Diphenylphosphine Oxide via Radical C-P and C-C Bond Formation.
Organic letters, 2016, 18, 4928-4931
1544264 CIFC21 H23 N O5P -19.996; 10.556; 11.033
69.226; 73.09; 65.04		973Han, Jing-Qiang; Zhang, Huan-Huan; Xu, Peng-Fei; Luo, Yong-Chun
Lewis Acid and (Hypo)iodite Relay Catalysis Allows a Strategy for the Synthesis of Polysubstituted Azetidines and Tetrahydroquinolines.
Organic letters, 2016, 18, 5212
1544265 CIFC20 H21 N O4P 1 21/n 19.7358; 9.6518; 19.991
90; 98.694; 90		1856.93Han, Jing-Qiang; Zhang, Huan-Huan; Xu, Peng-Fei; Luo, Yong-Chun
Lewis Acid and (Hypo)iodite Relay Catalysis Allows a Strategy for the Synthesis of Polysubstituted Azetidines and Tetrahydroquinolines.
Organic letters, 2016, 18, 5212
1544286 CIFC23 H21 N OP -110.2062; 13.2507; 13.9258
91.429; 104.805; 98.033		1799.3Roy, Tony; Thangaraj, Manikandan; Kaicharla, Trinadh; Kamath, Rupa V.; Gonnade, Rajesh G.; Biju, Akkattu T.
The Aryne [2,3] Stevens Rearrangement.
Organic letters, 2016, 18, 5428
1544319 CIFC40 H76 N10 O20 S4P 1 21/n 17.7136; 12.8367; 26.8813
90; 92.503; 90		2659.2Feng, Wei-Xu; van der Lee, Arie; Legrand, Yves-Marie; Petit, Eddy; Dumitrescu, Dan; Su, Cheng-Yong; Barboiu, Mihail
Adaptive Encapsulation of ω-Amino Acids and Their Guanidinium-Amide Congeners.
Organic letters, 2016, 18, 5556-5559
1544320 CIFC30 H54 N10 O17 S4P b c a18.5465; 16.3492; 28.7869
90; 90; 90		8728.8Feng, Wei-Xu; van der Lee, Arie; Legrand, Yves-Marie; Petit, Eddy; Dumitrescu, Dan; Su, Cheng-Yong; Barboiu, Mihail
Adaptive Encapsulation of ω-Amino Acids and Their Guanidinium-Amide Congeners.
Organic letters, 2016, 18, 5556-5559
1544321 CIFC28 H53 N2 Na2 O25.5 S4P -19.572; 19.0529; 22.861
89.387; 85.105; 89.819		4153.81Feng, Wei-Xu; van der Lee, Arie; Legrand, Yves-Marie; Petit, Eddy; Dumitrescu, Dan; Su, Cheng-Yong; Barboiu, Mihail
Adaptive Encapsulation of ω-Amino Acids and Their Guanidinium-Amide Congeners.
Organic letters, 2016, 18, 5556-5559
1544322 CIFC60 H102 N4 O20 S4P -112.658; 14.765; 19.6938
102.257; 99.362; 103.809		3403.4Feng, Wei-Xu; van der Lee, Arie; Legrand, Yves-Marie; Petit, Eddy; Dumitrescu, Dan; Su, Cheng-Yong; Barboiu, Mihail
Adaptive Encapsulation of ω-Amino Acids and Their Guanidinium-Amide Congeners.
Organic letters, 2016, 18, 5556-5559
1544323 CIFC30 H48 N10 O16 S4P -17.6006; 10.2393; 12.7741
96.042; 101.703; 91.37		967.02Feng, Wei-Xu; van der Lee, Arie; Legrand, Yves-Marie; Petit, Eddy; Dumitrescu, Dan; Su, Cheng-Yong; Barboiu, Mihail
Adaptive Encapsulation of ω-Amino Acids and Their Guanidinium-Amide Congeners.
Organic letters, 2016, 18, 5556-5559
1544337 CIFC26 H36 B F2 N3 OP -17.5729; 10.5422; 16.273
91.813; 99.198; 102.19		1250.7Li, Jin; Zhang, Qian; Yin, Jian; Yu, Changjiang; Cheng, Kai; Wei, Yun; Hao, Erhong; Jiao, Lijuan
Metal-Free and Versatile Synthetic Routes to Natural and Synthetic Prodiginines from Boron Dipyrrin.
Organic letters, 2016, 18, 5696-5699
1544338 CIFC11 H9 B Br2 F2 N2 O2P 1 21/n 17.1123; 13.579; 13.939
90; 100.474; 90		1323.8Li, Jin; Zhang, Qian; Yin, Jian; Yu, Changjiang; Cheng, Kai; Wei, Yun; Hao, Erhong; Jiao, Lijuan
Metal-Free and Versatile Synthetic Routes to Natural and Synthetic Prodiginines from Boron Dipyrrin.
Organic letters, 2016, 18, 5696-5699
1544342 CIFC38 H26 F10 O6P 1 21/n 18.1826; 25.666; 31.715
90; 95.407; 90		6631Grigalunas, Michael; Wiest, Olaf; Helquist, Paul
Single-Flask Multicomponent Synthesis of Highly Substituted α-Pyrones via a Sequential Enolate Arylation and Alkenylation Strategy.
Organic letters, 2016, 18, 5724-5727
1544343 CIFC28 H26.5 Cl2 O9.25P 1 21/c 127.9493; 14.6228; 26.5088
90; 105.098; 90		10460.1Grigalunas, Michael; Wiest, Olaf; Helquist, Paul
Single-Flask Multicomponent Synthesis of Highly Substituted α-Pyrones via a Sequential Enolate Arylation and Alkenylation Strategy.
Organic letters, 2016, 18, 5724-5727
1544348 CIFC11 H17 N O SiP 1 c 110.178; 10.104; 12.72
90; 108.216; 90		1242.5Liu, Pei; Tang, Jinghua; Zeng, Xiaoming
Site-Selective Silylation of Aliphatic C-H Bonds Mediated by [1,5]-Hydrogen Transfer: Synthesis of α-Sila Benzamides.
Organic letters, 2016, 18, 5536-5539
1544365 CIFC13 H10 O SP 1 21/c 113.6637; 5.6795; 13.4061
90; 96.068; 90		1034.52Wang, Ming; Fan, Qiaoling; Jiang, Xuefeng
Transition-Metal-Free Diarylannulated Sulfide and Selenide Construction via Radical/Anion-Mediated Sulfur-Iodine and Selenium-Iodine Exchange.
Organic letters, 2016, 18, 5756-5759
1544366 CIFC26 H19 IP b c a16.0575; 11.4137; 21.6746
90; 90; 90		3972.4Wang, Ming; Fan, Qiaoling; Jiang, Xuefeng
Transition-Metal-Free Diarylannulated Sulfide and Selenide Construction via Radical/Anion-Mediated Sulfur-Iodine and Selenium-Iodine Exchange.
Organic letters, 2016, 18, 5756-5759
1544383 CIFC32 H31 N3 O2 SP 1 21/n 116.708; 10.3275; 17.209
90; 110.656; 90		2778.6Li, Lixin; Liu, Peipei; Su, Yijin; Huang, Hanmin
Palladium-Catalyzed Aminomethylamination and Aromatization of Aminoalkenes with Aminals via C-N Bond Activation.
Organic letters, 2016, 18, 5736-5739
1544384 CIFC18 H17 F3 N2 O2 SP 1 21/c 113.134; 9.8729; 29.105
90; 93.355; 90		3767.6Li, Lixin; Liu, Peipei; Su, Yijin; Huang, Hanmin
Palladium-Catalyzed Aminomethylamination and Aromatization of Aminoalkenes with Aminals via C-N Bond Activation.
Organic letters, 2016, 18, 5736-5739
1544394 CIFC23 H22 OP -17.6465; 11.1436; 11.8808
116.215; 94.594; 107.174		841.15Chen, Xiaoyu; Day, David Philip; Teo, Wan Teng; Chan, Philip Wai Hong
Gold- and Brønsted Acid-Catalyzed Cycloisomerization of 1,8-Diynyl Vinyl Acetates to Bicyclo[2.2.1]hept-2-en-7-ones.
Organic letters, 2016, 18, 5936
1544423 CIFC12 H12 F N O3P 21 21 215.6649; 19.698; 20.708
90; 90; 90		2310.7Wu, Hongmiao; Yang, Bin; Zhu, Lin; Lu, Ronghua; Li, Guigen; Lu, Hongjian
High-Valent Palladium-Promoted Formal Wagner-Meerwein Rearrangement.
Organic letters, 2016, 18, 5804
1544424 CIFC16 H12 F N O3P 1 c 18.5173; 5.5799; 28.549
90; 95.813; 90		1349.8Wu, Hongmiao; Yang, Bin; Zhu, Lin; Lu, Ronghua; Li, Guigen; Lu, Hongjian
High-Valent Palladium-Promoted Formal Wagner-Meerwein Rearrangement.
Organic letters, 2016, 18, 5804
1544476 CIFC29 H20 Br N O2P 21 21 219.7525; 12.6566; 18.224
90; 90; 90		2249.5Shen, Hong-Qiang; Gao, Xiang; Liu, Cong; Hu, Shu-Bo; Zhou, Yong-Gui
A Hydrogenation/Oxidative Fragmentation Cascade for Synthesis of Chiral 4,5-Dihydro-1H-benzo[d]azepin-1-ones.
Organic letters, 2016, 18, 5920-5923
1544477 CIFC22 H17 N O2P 21 21 219.2696; 12.0477; 15.0296
90; 90; 90		1678.47Shen, Hong-Qiang; Gao, Xiang; Liu, Cong; Hu, Shu-Bo; Zhou, Yong-Gui
A Hydrogenation/Oxidative Fragmentation Cascade for Synthesis of Chiral 4,5-Dihydro-1H-benzo[d]azepin-1-ones.
Organic letters, 2016, 18, 5920-5923
1544508 CIFC29 H23 Cl N4 O2P -111.0894; 11.1837; 11.8059
63.655; 83.383; 68.088		1215.08Zhou, Xiaorong; Fan, Zili; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization.
Organic letters, 2016, 18, 4706-4709
1544521 CIFC26 H32 N2 O4 SiP 1 21/n 111.118; 19.642; 12.625
90; 110.85; 90		2576.5Deng, Yongming; Pei, Chao; Arman, Hadi; Dong, Kuiyong; Xu, Xinfang; Doyle, Michael P.
Syntheses of Tetrahydropyridazine and Tetrahydro-1,2-diazepine Scaffolds through Cycloaddition Reactions of Azoalkenes with Enol Diazoacetates.
Organic letters, 2016, 18, 5884-5887
1544522 CIFC20 H18 N2 O4C 1 2/c 135.35; 5.606; 21.4
90; 124.417; 90		3498Deng, Yongming; Pei, Chao; Arman, Hadi; Dong, Kuiyong; Xu, Xinfang; Doyle, Michael P.
Syntheses of Tetrahydropyridazine and Tetrahydro-1,2-diazepine Scaffolds through Cycloaddition Reactions of Azoalkenes with Enol Diazoacetates.
Organic letters, 2016, 18, 5884-5887
1544523 CIFC26 H32 N4 O4 SiP -111.071; 13.272; 18.896
78.005; 87.787; 84.779		2704Deng, Yongming; Pei, Chao; Arman, Hadi; Dong, Kuiyong; Xu, Xinfang; Doyle, Michael P.
Syntheses of Tetrahydropyridazine and Tetrahydro-1,2-diazepine Scaffolds through Cycloaddition Reactions of Azoalkenes with Enol Diazoacetates.
Organic letters, 2016, 18, 5884-5887
1544524 CIFC17 H18 B Br F4 N4P 1 21/n 19.3019; 20.691; 10.107
90; 96.604; 90		1932.3Joshi, Madhur S.; Pigge, F. Christopher
Construction of 1,2,4-Triazole Derivatives via Cyclocondensation of Alkylidene Dihydropyridines and Aryldiazonium Salts.
Organic letters, 2016, 18, 5916-5919
1544537 CIFC49 H10 Au F15 I4 N4P 1 21/c 17.33; 22.65; 28.2
90; 101.877; 90		4582Soll, Matan; Sudhakar, Kolanu; Fridman, Natalia; Müller, Alexander; Röder, Beate; Gross, Zeev
One-Pot Conversion of Fluorophores to Phosphorophores.
Organic letters, 2016, 18, 5840-5843
1544538 CIFC37.66667 H8.66667 Au Cl2 F15 N4I 41/a :221.092; 21.092; 45.876
90; 90; 90		20409Soll, Matan; Sudhakar, Kolanu; Fridman, Natalia; Müller, Alexander; Röder, Beate; Gross, Zeev
One-Pot Conversion of Fluorophores to Phosphorophores.
Organic letters, 2016, 18, 5840-5843
1544539 CIFC38 H6 Cl2 Cu F15 I4 N4P 1 21/c 120.019; 13.865; 15.727
90; 111.499; 90		4061.5Soll, Matan; Sudhakar, Kolanu; Fridman, Natalia; Müller, Alexander; Röder, Beate; Gross, Zeev
One-Pot Conversion of Fluorophores to Phosphorophores.
Organic letters, 2016, 18, 5840-5843
1544698 CIFC23 H26 N2 O4 SP 1 21/c 18.7498; 12.278; 20.161
90; 100.27; 90		2131.2Zheng, Jia; Li, Zun; Wu, Wanqing; Jiang, Huanfeng
Controllable O-Nucleometalation Cyclization Strategy: Access to Divergent Ring-Functionalized Molecules.
Organic letters, 2016, 18, 6232-6235
1544699 CIFC15 H18 N2 O4 SP -18.239; 9.8871; 10.5292
95.163; 109.34; 104.536		769.2Zheng, Jia; Li, Zun; Wu, Wanqing; Jiang, Huanfeng
Controllable O-Nucleometalation Cyclization Strategy: Access to Divergent Ring-Functionalized Molecules.
Organic letters, 2016, 18, 6232-6235
1544700 CIFC21 H22 N2 O4 SP -18.3281; 10.784; 12.649
70.74; 73.72; 67.38		974.5Zheng, Jia; Li, Zun; Wu, Wanqing; Jiang, Huanfeng
Controllable O-Nucleometalation Cyclization Strategy: Access to Divergent Ring-Functionalized Molecules.
Organic letters, 2016, 18, 6232-6235
1555479 CIFC24 H8 Br2 N2P 1 21/n 111.5512; 7.5173; 22.879
90; 91.554; 90		1985.9Min, Lijun; Pan, Bin; Gu, Yanlong
Synthesis of Quinoline-Fused 1-Benzazepines through a Mannich-Type Reaction of a C,N-Bisnucleophile Generated from 2-Aminobenzaldehyde and 2-Methylindole.
Organic letters, 2016, 18, 364-367
1555484 CIFC16 H24 N3 O3 PP b c a28.26; 11.505; 11.128
90; 90; 90		3618Ahamad, Shakir; Kant, Ruchir; Mohanan, Kishor
Metal-Free Three-Component Domino Approach to Phosphonylated Triazolines and Triazoles.
Organic letters, 2016, 18, 280-283
1555485 CIFC22 H13 Cl F N3 O SP n a 2117.7894; 18.2676; 5.7336
90; 90; 90		1863.2Fan, Wei; Li, Qun; Li, Yanrong; Sun, Hao; Jiang, Bo; Li, Guigen
I2/O2-Enabled N-S Bond Formation to Access Functionalized 1,2,3-Thiadiazoles.
Organic letters, 2016, 18, 1258-1261
1555486 CIFC25 H19.78 N3 O2.39 PdP -18.4976; 11.7441; 20.5928
80.687; 83.765; 78.031		1977.91Wiest, Johannes M.; Pöthig, Alexander; Bach, Thorsten
Pyrrole as a Directing Group: Regioselective Pd(II)-Catalyzed Alkylation and Benzylation at the Benzene Core of 2-Phenylpyrroles.
Organic letters, 2016, 18, 852-855
1555487 CIFC20 H21 N O2P b c a14.6593; 7.8044; 27.406
90; 90; 90		3135.4Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555488 CIFC17 H17 N O SP 1 21/c 18.6142; 9.0565; 18.42
90; 103.352; 90		1398.18Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555489 CIFC15 H17 N OP 1 21/n 114.5023; 8.2306; 20.0369
90; 98.744; 90		2363.9Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555490 CIFC19 H19 N OP b c a13.21; 7.8624; 27.4014
90; 90; 90		2846Nandi, Raj Kumar; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles.
Organic letters, 2016, 18, 1716-1719
1555491 CIFC23 H29 N O4 SP -19.523; 9.6405; 11.7824
83.18; 76.85; 71.05		995.1Murai, Kenichi; Matsuura, Kei; Aoyama, Hiroshi; Fujioka, Hiromichi
Oxidative Rearrangement via in Situ Generated N-Chloroamine: Synthesis of Fused Tetrahydroisoquinolines.
Organic letters, 2016, 18, 1314-1317
1555492 CIFC16 H17 N3 O3P -18.6512; 13.1178; 13.2085
94.755; 97.921; 102.375		1440.34Zhang, Lin-Bao; Zhang, Shou-Kun; Wei, Donghui; Zhu, Xinju; Hao, Xin-Qi; Su, Jian-Hang; Niu, Jun-Long; Song, Mao-Ping
Cobalt(II)-Catalyzed C-H Amination of Arenes with Simple Alkylamines.
Organic letters, 2016, 18, 1318-1321
1555493 CIFC17 H21 NP -16.0723; 8.6709; 14.006
75.45; 78.72; 70.16		666.5Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555494 CIFC19 H33 N O6P 1 21/c 119.714; 6.3466; 16.045
90; 90.8; 90		2007.3Schweighauser, Luca; Bodoky, Ina; Kessler, Simon N.; Häussinger, Daniel; Donsbach, Carsten; Wegner, Hermann A.
Bidentate Lewis Acid Catalyzed Domino Diels-Alder Reaction of Phthalazine for the Synthesis of Bridged Oligocyclic Tetrahydronaphthalenes.
Organic letters, 2016, 18, 1330-1333
1555495 CIFC24 H22 Br N3 O5.5P 21 21 2112.8376; 12.9227; 14.0967
90; 90; 90		2338.59Kumarswamyreddy, Nandarapu; Kesavan, Venkitasamy
Enantioselective Synthesis of Dihydrospiro[indoline-3,4'-pyrano[2,3-c]pyrazole] Derivatives via Michael/Hemiketalization Reaction.
Organic letters, 2016, 18, 1354-1357
1555496 CIFC25 H22 F N O2P 21 21 219.56524; 18.64102; 22.57118
90; 90; 90		4024.57Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555497 CIFC25 H22 Cl N O2P 1 21 110.8203; 8.0501; 11.8593
90; 90.3984; 90		1032.97Ošeka, Maksim; Kimm, Mariliis; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, Tõnis
Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles.
Organic letters, 2016, 18, 1358-1361
1555498 CIFC88 H89 B3 N6P 1 21/n 19.8983; 28.293; 24.5786
90; 96.552; 90		6838.3Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555499 CIFC45 H51 B3 F6 N6P 1 21/n 116.672; 6.7638; 37.518
90; 99.692; 90		4170.4Qiu, Feng; Zhang, Fan; Tang, Ruizhi; Fu, Yubin; Wang, Xinyang; Han, Sheng; Zhuang, Xiaodong; Feng, Xinliang
Triple Boron-Cored Chromophores Bearing Discotic 5,11,17-Triazatrinaphthylene-Based Ligands.
Organic letters, 2016, 18, 1398-1401
1555500 CIFC19 H26 O3P 21 21 216.43415; 13.9695; 18.8234
90; 90; 90		1691.88Lin, Han; Xiao, Li-Jun; Zhou, Min-Jie; Yu, Hong-Ming; Xie, Jian-Hua; Zhou, Qi-Lin
Enantioselective Approach to (-)-Hamigeran B and (-)-4-Bromohamigeran B via Catalytic Asymmetric Hydrogenation of Racemic Ketone To Assemble the Chiral Core Framework.
Organic letters, 2016, 18, 1434-1437
1555501 CIFC20 H20 O7P 1 21/c 113.364; 7.917; 21.513
90; 127.54; 90		1804.8More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555502 CIFC21 H24 O6P 1 21/c 111.9383; 10.2634; 15.2907
90; 97.621; 90		1857More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555503 CIFC11 H12 O3P -17.2646; 8.0955; 8.184
90.831; 97.639; 93.425		476.06More, Atul A.; Ramana, Chepuri V.
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade.
Organic letters, 2016, 18, 1458-1461
1555504 CIFC33 H37 Cl N2 O6C 1 2/c 125.162; 15.406; 16.174
90; 109.269; 90		5919Di Maso, Michael J.; Nepomuceno, Gabriella M.; St Peter, Michael A.; Gitre, Haley H.; Martin, Kevin S.; Shaw, Jared T.
Synthesis of (±)-Bisavenanthramide B-6 by an Anionic Anhydride Mannich Reaction.
Organic letters, 2016, 18, 1740-1743
1555505 CIFC164 H260 N4 O75 S3P 21 21 2118.0825; 18.5554; 56.7015
90; 90; 90		19024.9Inouye, Masahiko; Yoshizawa, Atsushi; Shibata, Mari; Yonenaga, Yuki; Fujimoto, Kazuhisa; Sakata, Takuma; Matsumoto, Shinya; Shiro, Motoo
Cyclodextrin-Isolated Alkynylpyrenes as UV-Stable and Blue-Light-Emitting Molecules Even in Condensed States.
Organic letters, 2016, 18, 1960-1963
1555506 CIFC13 H18 O1.5P 1 21 110.2913; 7.9908; 13.7239
90; 97.986; 90		1117.65Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555507 CIFC26 H38 O3P 1 21 110.3364; 8.2959; 12.9455
90; 96.995; 90		1101.81Kakde, Badrinath N.; Kumar, Nivesh; Mondal, Pradip Kumar; Bisai, Alakesh
Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization: Total Synthesis of Akaol A.
Organic letters, 2016, 18, 1752-1755
1555508 CIFC18 H21 N O5P 1 21/n 112.4616; 7.5556; 17.8282
90; 109.236; 90		1584.9Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555509 CIFC17 H18 Cl N O5P 21 21 216.891; 11.883; 20.413
90; 90; 90		1671.5Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555510 CIFC23 H23 N O5P 1 21/n 116.5186; 6.7973; 17.4934
90; 97.222; 90		1948.6Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555511 CIFC17 H19 N O5P 21 21 217.7825; 12.1682; 16.9656
90; 90; 90		1606.63Raja, Arun; Hong, Bor-Cherng; Liao, Ju-Hsiou; Lee, Gene-Hsiang
Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons.
Organic letters, 2016, 18, 1760-1763
1555512 CIFC26 H22 N3 O2 PP 1 21/c 111.3945; 16.435; 12.4553
90; 107.236; 90		2227.7Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555513 CIFC26 H22 N3 O2 PP 1 21/c 110.704; 21.3272; 11.2625
90; 120.672; 90		2211.4Zheng, Jing; Zhang, Yan; Wang, Dahai; Cui, Sunliang
Silver(I)-Mediated Phosphorylation/Cyclization Cascade of N-Cyanamide Alkenes for Divergent Access to Quinazolinones and Dihydroisoquinolinones.
Organic letters, 2016, 18, 1768-1771
1555514 CIFC21 H28 O4P 1 21/c 115.5552; 15.6415; 8.1031
90; 94.596; 90		1965.2Elliott, Daniel C.; Ma, Tsz-Kan; Selmani, Aymane; Cookson, Rosa; Parsons, Philip J.; Barrett, Anthony G. M.
Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates.
Organic letters, 2016, 18, 1800-1803
1555515 CIFC19 H16 Cl N O2P 1 21/c 112.568; 7.479; 17.461
90; 108.353; 90		1557.8Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555516 CIFC19 H17 N O2P -18.206; 8.581; 10.584
90.785; 100.066; 104.431		709.4Kotha, Sambasivarao; Aswar, Vikas R.
Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes.
Organic letters, 2016, 18, 1808-1811
1555517 CIFC15 H16 O3R -3 :H29.475; 29.475; 7.245
90; 90; 120		5451Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555518 CIFC18 H22 O5P 1 21/n 16.613; 28.29; 8.886
90; 103.404; 90		1617.1Li, Xiaoyu; Liu, Xiaoyu; Jiao, Xiaozhen; Yang, Hongguang; Yao, Yangyang; Xie, Ping
An approach to (±)-Lingzhiol.
Organic letters, 2016, 18, 1944-1946
1555519 CIFC13 H15 Br Cl N O2P 1 21/c 110.4382; 24.2507; 10.9589
90; 95.0262; 90		2763.4Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555520 CIFC9 H7 Cl N2P 1 21/c 19.8146; 3.9248; 20.553
90; 103.021; 90		771.35Wang, Mengzhou; Zhang, Yanyan; Wang, Tao; Wang, Chao; Xue, Dong; Xiao, Jianliang
Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one.
Organic letters, 2016, 18, 1976-1979
1555521 CIFC23 H16 F2 N4 O2P 1 21 17.8577; 14.9042; 9.3787
90; 113.529; 90		1007.05Qiao, Jin-Bao; Zhao, Yu-Ming; Gu, Peiming
Asymmetric Intramolecular Desymmetrization of meso-α,α'-Diazido Alcohols with Aryldiazoacetates: Assembly of Chiral C3 Fragments with Three Continuous Stereocenters.
Organic letters, 2016, 18, 1984-1987
1555522 CIFC15 H21 N3 O3P -16.433; 7.542; 15.771
90.874; 95.675; 109.593		716.4Mehr, S Hessam M; Patrick, Brian O.; MacLachlan, Mark J.
Stabilization of a Strained Heteroradialene by Peripheral Electron Delocalization.
Organic letters, 2016, 18, 1840-1843
1555523 CIFC17 H25 Cl F N OP 1 21/c 113.3762; 9.6596; 13.4588
90; 93.8818; 90		1735.01Hamel, Jean-Denys; Cloutier, Mélissa; Paquin, Jean-François
Exploiting a Difference in Leaving Group Ability: An Approach to β-Substituted Monofluoroalkenes Using gem-Chlorofluoropropenes.
Organic letters, 2016, 18, 1852-1855
1555524 CIFC20 H14P 1 21 16.4855; 7.5481; 13.9074
90; 95.824; 90		677.3Zhou, Yujing; Ye, Fei; Zhou, Qi; Zhang, Yan; Wang, Jianbo
Cu(I)-Catalyzed Tandem Reaction of Carbene Coupling and Horner-Wadsworth-Emmons Type Olefination: Access toward Enynes.
Organic letters, 2016, 18, 2024-2027
1555525 CIFC23 H39 N O3 S SiP 21 21 2111.2183; 17.958; 25.733
90; 90; 90		5184.1Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555526 CIFC25 H37 N3 O3P 21 21 218.174; 12.797; 21.823
90; 90; 90		2282.7Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555527 CIFC21 H33 N O5P 21 21 211.42; 19.1624; 9.3685
90; 90; 90		2050.2Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555528 CIFC18 H31 N O5P 21 21 217.71375; 8.88494; 28.0459
90; 90; 90		1922.16Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555529 CIFC21 H31 N O5P 1 21 111.5555; 6.7668; 12.9264
90; 98.846; 90		998.74Xu, Bing; Li, Guang; Li, Jing; Shi, Yian
Total Synthesis of the Proposed Structure of Marineosin A.
Organic letters, 2016, 18, 2028-2031
1555530 CIFC38 H22P 1 21/n 117.4392; 7.3355; 17.5242
90; 94.296; 90		2235.49Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555531 CIFC36 H18P 1 21/c 112.7866; 3.9237; 42.438
90; 95.156; 90		2120.53Hsieh, Ya-Chu; Wu, Tsun-Cheng; Li, Jen-Yi; Chen, Yi-Ting; Kuo, Ming-Yu; Chou, Pi-Tai; Wu, Yao-Ting
Dinaphthozethrene and Diindenozethrene: Synthesis, Structural Analysis, and Properties.
Organic letters, 2016, 18, 1868-1871
1555532 CIFC15 H11 Br N2 OP 1 21/c 17.5865; 11.136; 15.609
90; 96.63; 90		1309.9Wang, Jie; Zha, Shanke; Chen, Kehao; Zhang, Feifei; Song, Chao; Zhu, Jin
Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C-H Functionalization of Benzimidates with Dioxazolones.
Organic letters, 2016, 18, 2062-2065
1555533 CIFC20 H20 O2 S2P 1 21/n 110.3493; 16.6118; 11.4274
90; 116.111; 90		1764.1Lai, Junshan; Liang, Yongping; Liu, Teng; Tang, Shouchu
Dithiane Induced Cycloaddition/Aromatization Tactic for the Synthesis of Multisubstituted Furans.
Organic letters, 2016, 18, 2066-2069
1555534 CIFC20 H28 N2 O3P 1 21 19.7442; 6.1717; 14.9524
90; 90.609; 90		899.16Hsieh, Sheng-Ying; Bode, Jeffrey W.
Silicon Amine Reagents for the Photocatalytic Synthesis of Piperazines from Aldehydes and Ketones.
Organic letters, 2016, 18, 2098-2101
1555535 CIFC19 H25 Cl N O RhP 1 21/c 113.0578; 15.8566; 18.5108
90; 91.055; 90		3832.1Wang, Qiang; Li, Xingwei
Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis.
Organic letters, 2016, 18, 2102-2105
1555536 CIFC15 H15 Br O3 SP 1 21 15.92604; 12.2676; 9.9444
90; 103.755; 90		702.21Pagire, Santosh K.; Paria, Suva; Reiser, Oliver
Synthesis of β-Hydroxysulfones from Sulfonyl Chlorides and Alkenes Utilizing Visible Light Photocatalytic Sequences.
Organic letters, 2016, 18, 2106-2109
1555537 CIFC46 H39 Au2 F6 N O5 P2 S3P 1 c 114.011; 16.7528; 20.7802
90; 105.001; 90		4711.4Tamai, Taichi; Fujiwara, Keiko; Higashimae, Shinya; Nomoto, Akihiro; Ogawa, Akiya
Gold-Catalyzed Anti-Markovnikov Selective Hydrothiolation of Unactivated Alkenes.
Organic letters, 2016, 18, 2114-2117
1555538 CIFC12 H13 N O2P 1 21/n 19.8079; 8.8394; 12.567
90; 99.596; 90		1074.3Fraboni, Americo J.; Brenner-Moyer, Stacey E
Dienamine-Catalyzed Nitrone Formation via Redox Reaction.
Organic letters, 2016, 18, 2146-2149
1555539 CIFC16 H15 Br Cl3 N O2P -17.5091; 10.1225; 12.5419
76.957; 81.066; 75.302		893.46García-García, Carolina; Ortiz-Rojano, Laura; Álvarez, Susana; Álvarez, Rosana; Ribagorda, María; Carreño, M Carmen
Friedel-Crafts Alkylation of Indoles with p-Quinols: The Role of Hydrogen Bonding of Water for the Desymmetrization of the Cyclohexadienone System.
Organic letters, 2016, 18, 2224-2227
1555540 CIFC17 H11 N OP -13.991; 10.967; 15.118
73.536; 86.417; 81.507		627.5Wang, Lianjie; Liu, Xiaocui; Wang, Mang; Liu, Jun
Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans.
Organic letters, 2016, 18, 2162-2165
1555541 CIFC20 H27 O3.5I 4119.7536; 19.7536; 9.0366
90; 90; 90		3526.1Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555542 CIFC20 H26 O3P 21 21 219.7169; 10.1381; 17.5286
90; 90; 90		1726.76Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555543 CIFC22 H32 O4C 1 2 118.2916; 8.7712; 12.993
90; 103.232; 90		2029.24Wan, Luo-Sheng; Nian, Yin; Ye, Chen-Jun; Shao, Li-Dong; Peng, Xing-Rong; Geng, Chang-An; Zuo, Zhi-Li; Li, Xiao-Nian; Yang, Jian; Zhou, Ming; Qiu, Ming-Hua
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus.
Organic letters, 2016, 18, 2166-2169
1555544 CIFC22 H20 Br N O2P 1 21 18.6651; 5.8524; 18.9495
90; 93.712; 90		958.94Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555545 CIFC24 H25 N O4P 112.7971; 12.8656; 14.0933
88.968; 86.108; 66.582		2124.21Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555546 CIFC28 H25 N O2P 21 21 215.9977; 8.669; 42.0392
90; 90; 90		2185.79Ruchti, Jonathan; Carreira, Erick M.
Rh-Catalyzed Stereospecific Synthesis of Allenes from Propargylic Benzoates and Arylboronic Acids.
Organic letters, 2016, 18, 2174-2176
1555547 CIFC40 H40 N2 O SP -110.2707; 12.5581; 14.2615
78.265; 69.761; 81.577		1684Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555548 CIFC26 H25 Cl2 N O4 SP -19.9795; 10.2314; 12.8722
92.489; 106.194; 96.538		1250.1Makarov, Anton S.; Merkushev, Anton A.; Uchuskin, Maxim G.; Trushkov, Igor V.
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues.
Organic letters, 2016, 18, 2192-2195
1555549 CIFC21 H15 NP -110.3062; 11.6276; 13.2088
75.92; 88.72; 87.09		1533.28Saunthwal, Rakesh K.; Patel, Monika; Verma, Akhilesh K.
Metal- and Protection-Free [4 + 2] Cycloadditions of Alkynes with Azadienes: Assembly of Functionalized Quinolines.
Organic letters, 2016, 18, 2200-2203
1555550 CIFC12 H9 F3 N2 OP 1 21/c 19.3458; 13.3878; 9.015
90; 104.592; 90		1091.57Nguyen, Thanh Binh; Ermolenko, Ludmila; Retailleau, Pascal; Al-Mourabit, Ali
Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2-Aminopyrimidine and 2-Aminopyridines.
Organic letters, 2016, 18, 2177-2179
1555551 CIFC16 H18 N2 O2P 1 21 18.94706; 11.2291; 14.9983
90; 102.552; 90		1470.83Halskov, Kim Søholm; Næsborg, Line; Tur, Fernando; Jørgensen, Karl Anker
Asymmetric [3 + 2] Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Aldehydes by Synergistic Palladium and Organocatalysis.
Organic letters, 2016, 18, 2220-2223
1555552 CIFC8 H9 Cl N4 OP 21 21 215.3345; 17.4841; 6.9026
90; 90; 90		1850.7Sun, Huan-Li; Chen, Fei; Xie, Ming-Sheng; Guo, Hai-Ming; Qu, Gui-Rong; He, Yan-Mei; Fan, Qing-Hua
Asymmetric Hydrogenation of α-Purine Nucleobase-Substituted Acrylates with Rhodium Diphosphine Complexes: Access to Tenofovir Analogues.
Organic letters, 2016, 18, 2260-2263
1555553 CIFC18 H22 F N O4P 21 21 219.7821; 11.5835; 14.8591
90; 90; 90		1683.7Zhu, Luyi; Chen, Qiliang; Shen, Dan; Zhang, Weihao; Shen, Cong; Zeng, Xiaofei; Zhong, Guofu
Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction.
Organic letters, 2016, 18, 2387-2390
1555554 CIFC28 H24 O6 S2P 1 21/c 116.268; 7.4469; 22.374
90; 110.413; 90		2540.3Ni, Chunjie; Wang, MingLi; Tong, Xiaofeng
Access to Thiophene and 1H-Pyrrole via Amine-Initiated (3 + 2) Annulation and Aromatization Cascade Reaction of β'-Acetoxy Allenoate and 1,2-Bisnucleophile.
Organic letters, 2016, 18, 2240-2243

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