Crystallography Open Database

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1503034 CIFC18 H25 N O5P 1 21/c 111.2417; 12.5001; 12.3596
90; 111.39; 90		1617.17Lazarski, Kiel E.; Hu, Dennis X.; Stern, Charlotte L.; Thomson, Regan J.
A synthesis of the carbocyclic core of maoecrystal V.
Organic letters, 2010, 12, 3010-3013
1503035 CIFC24 H40 O3 SiP c a 2120.0329; 6.5664; 17.1418
90; 90; 90		2254.9Lazarski, Kiel E.; Hu, Dennis X.; Stern, Charlotte L.; Thomson, Regan J.
A synthesis of the carbocyclic core of maoecrystal V.
Organic letters, 2010, 12, 3010-3013
1503036 CIFC22 H23 N O7P 1 21/c 111.5178; 9.26; 18.695
90; 95.335; 90		1985.3Chattopadhyay, Kalicharan; Jana, Ranjan; Day, Victor W.; Douglas, Justin T.; Tunge, Jon A.
Mechanistic origin of the stereodivergence in decarboxylative allylation.
Organic letters, 2010, 12, 3042-3045
1503037 CIFC21 H22 O5P -18.8899; 13.526; 15.808
76.043; 82.036; 75.272		1778.1Chattopadhyay, Kalicharan; Jana, Ranjan; Day, Victor W.; Douglas, Justin T.; Tunge, Jon A.
Mechanistic origin of the stereodivergence in decarboxylative allylation.
Organic letters, 2010, 12, 3042-3045
1503038 CIFC72 H64 Cl8 O6 S8P -111.535; 15.772; 20.813
81.708; 89.14; 85.925		3737Shao, Min; Dongare, Prateek; Dawe, Louise N.; Thompson, David W.; Zhao, Yuming
Biscrown-annulated TTFAQ-dianthracene hybrid: synthesis, structure, and metal ion sensing.
Organic letters, 2010, 12, 3050-3053
1503039 CIFC18 H21 N3 O3P 1 21/c 116.143; 6.4594; 17.674
90; 116.29; 90		1652.3Chu, Wei-Jun; Yang, Yong; Chen, Chuan-Feng
Multiple hydrogen-bond-mediated molecular duplexes based on the self-complementary amidourea motif.
Organic letters, 2010, 12, 3156-3159
1503040 CIFC39 H50 N2 O3P -18.6711; 8.765; 24.82
97.279; 92.24; 117.315		1652.4Curiel, David; Más-Montoya, Miriam; Uruvakili, Anasuyama; Orenes, Raúl A; Pallamreddy, Haranath; Molina, Pedro
Synthesis and characterization of new carbazolocarbazoles: toward pi-extended N-fused heteroacenes
Organic letters, 2010, 12, 3164-3167
1503041 CIFC15 H11 N3 O2P 1 21/c 13.8217; 19.331; 16.505
90; 92.7; 90		1218Moustafa, Mahmoud M Abd Rabo; Pagenkopf, Brian L.
Synthesis of 5-azaindoles via a cycloaddition reaction between nitriles and donor-acceptor cyclopropanes.
Organic letters, 2010, 12, 3168-3171
1503042 CIFC25 H19 N O5P 1 21/c 112.2495; 9.5744; 17.716
90; 103.227; 90		2022.6Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503043 CIFC23 H13 Cl N2 O3C 1 2/c 133.018; 11.8272; 9.8005
90; 103.131; 90		3727.1Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503044 CIFC34 H43 O2 PP -112.4771; 12.5044; 12.6807
113.793; 99.156; 114.617		1513.1Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503045 CIFC30 H42 N O5 PP -18.2518; 8.748; 20.7225
84.633; 84.557; 82.321		1470.83Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503046 CIFC28 H38 N O PP 1 21/n 113.0677; 13.0609; 15.1264
90; 100.924; 90		2534.93Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503047 CIFC34 H46 Cl O3 PC 1 2/c 123.91; 10.4217; 28.342
90; 108.506; 90		6697.1Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503048 CIFC29 H18 Br2 O2P -19.8049; 11.3545; 12.1899
105.88; 93.794; 100.857		1271.95Kao, Tzu-Ting; Syu, Siang-en; Jhang, Yi-Wun; Lin, Wenwei
Preparation of tetrasubstituted furans via intramolecular Wittig reactions with phosphorus ylides as intermediates.
Organic letters, 2010, 12, 3066-3069
1503049 CIFC22 H24 N6 O3P 1 21 18.0218; 14.6605; 18.8312
90; 96.776; 90		2199.1Yan, Wuming; Wang, Qiaoyi; Chen, Yunfeng; Petersen, Jeffrey L.; Shi, Xiaodong
Iron-catalyzed C-O bond activation for the synthesis of propargyl-1,2,3-triazoles and 1,1-bis-triazoles.
Organic letters, 2010, 12, 3308-3311
1503050 CIFC23 H17 N3P 1 21/c 115.3847; 5.6909; 40.749
90; 96.166; 90		3547Yan, Wuming; Wang, Qiaoyi; Chen, Yunfeng; Petersen, Jeffrey L.; Shi, Xiaodong
Iron-catalyzed C-O bond activation for the synthesis of propargyl-1,2,3-triazoles and 1,1-bis-triazoles.
Organic letters, 2010, 12, 3308-3311
1503051 CIFC27 H25 N O3 SP 1 21/c 118.133; 12.922; 9.6356
90; 102.83; 90		2201.4Li, Changkun; Zhang, Hang; Feng, Jiajie; Zhang, Yan; Wang, Jianbo
Rh(I)-catalyzed carbonylative carbocyclization of tethered ene- and yne-cyclopropenes.
Organic letters, 2010, 12, 3082-3085
1503052 CIFC30 H29 N O3 SC 1 2/c 121.763; 10.484; 23.818
90; 111.79; 90		5046Li, Changkun; Zhang, Hang; Feng, Jiajie; Zhang, Yan; Wang, Jianbo
Rh(I)-catalyzed carbonylative carbocyclization of tethered ene- and yne-cyclopropenes.
Organic letters, 2010, 12, 3082-3085
1503053 CIFC26 H25 N O2 SP 1 21/c 124.46; 7.3613; 12.014
90; 92.99; 90		2160.3Li, Changkun; Zhang, Hang; Feng, Jiajie; Zhang, Yan; Wang, Jianbo
Rh(I)-catalyzed carbonylative carbocyclization of tethered ene- and yne-cyclopropenes.
Organic letters, 2010, 12, 3082-3085
1503054 CIFC36 H67 Br P2 PdP 1 21/n 113.092; 12.645; 23.224
90; 106.336; 90		3689Li, Hongbo; Grasa, Gabriela A.; Colacot, Thomas J.
A highly efficient, practical, and general route for the synthesis of (R3P)2Pd(0): structural evidence on the reduction mechanism of Pd(II) to Pd(0).
Organic letters, 2010, 12, 3332-3335
1503055 CIFC18 H30 Br2 O2 Pd2P 1 21/c 110.5941; 6.5221; 15.431
90; 104.263; 90		1033.4Li, Hongbo; Grasa, Gabriela A.; Colacot, Thomas J.
A highly efficient, practical, and general route for the synthesis of (R3P)2Pd(0): structural evidence on the reduction mechanism of Pd(II) to Pd(0).
Organic letters, 2010, 12, 3332-3335
1503056 CIFC20 H19 O4 PC 1 2/c 127.553; 8.908; 17.38
90; 125.364; 90		3479Zhang, Dong; Celaje, Jeff A.; Agua, Alon; Doan, Chad; Stewart, Timothy; Bau, Robert; Selke, Matthias
Photooxidation of mixed aryl and biarylphosphines.
Organic letters, 2010, 12, 3100-3103
1503057 CIFC20 H19 O3 PP 1 21/c 19.336; 12.036; 15.354
90; 101.625; 90		1689.9Zhang, Dong; Celaje, Jeff A.; Agua, Alon; Doan, Chad; Stewart, Timothy; Bau, Robert; Selke, Matthias
Photooxidation of mixed aryl and biarylphosphines.
Organic letters, 2010, 12, 3100-3103
1503058 CIFC72 H50 Fe2 O2P 1 21/n 114.141; 10.6057; 18.01
90; 109.354; 90		2548.4Morisaki, Yasuhiro; Sawamura, Toshiyuki; Murakami, Takuya; Chujo, Yoshiki
Synthesis of anthracene-stacked oligomers and polymer.
Organic letters, 2010, 12, 3188-3191
1503059 CIFC26 H37 N O5P c a 2116.5169; 5.7641; 50.954
90; 90; 90		4851.1Burke, Jason P.; Sabat, Michal; Iovan, Diana A.; Myers, William H.; Chruma, Jason J.
Exploring the original proposed biosynthesis of (+)-symbioimine: remote exocyclic stereocontrol in a type I IMDA reaction.
Organic letters, 2010, 12, 3192-3195
1503060 CIFC16 H20 N4 O7P 1 21 19.757; 29.99; 11.97
90; 98.61; 90		3463Medeiros, Matthew R.; Narayan, Radha S.; McDougal, Nolan T.; Schaus, Scott E.; Porco, Jr, John A
Skeletal diversity via cationic rearrangements of substituted dihydropyrans.
Organic letters, 2010, 12, 3222-3225
1503061 CIFC21 H32 N6 OP 1 21/n 111.9147; 20.442; 18.076
90; 97.6; 90		4363.9Mani, Ganesan; Jana, Debasish; Kumar, Rajnish; Ghorai, Debasish
Azatripyrrolic and azatetrapyrrolic macrocycles from the Mannich reaction of pyrrole: receptors for anions.
Organic letters, 2010, 12, 3212-3215
1503062 CIFC28 H42 N8 OP 1 21/c 112.9325; 14.018; 17.516
90; 109.805; 90		2987.6Mani, Ganesan; Jana, Debasish; Kumar, Rajnish; Ghorai, Debasish
Azatripyrrolic and azatetrapyrrolic macrocycles from the Mannich reaction of pyrrole: receptors for anions.
Organic letters, 2010, 12, 3212-3215
1503063 CIFC32 H50 N8 OP 1 21/c 117.429; 13.793; 15.399
90; 114.644; 90		3364.7Mani, Ganesan; Jana, Debasish; Kumar, Rajnish; Ghorai, Debasish
Azatripyrrolic and azatetrapyrrolic macrocycles from the Mannich reaction of pyrrole: receptors for anions.
Organic letters, 2010, 12, 3212-3215
1503064 CIFC29 H27.33 Cl2.67 N2 O2P -19.706; 11.437; 12.864
92.632; 108.562; 103.893		1302.4D'Souza, Daniel M; Muschelknautz, Christian; Rominger, Frank; Müller, Thomas J J
Unusual solid-state luminescent push-pull indolones: a general one-pot three-component approach.
Organic letters, 2010, 12, 3364-3367
1503065 CIFC40 H41 N3 O5 SP 1 21/n 119.1627; 9.8124; 19.8246
90; 97.067; 90		3699.3D'Souza, Daniel M; Muschelknautz, Christian; Rominger, Frank; Müller, Thomas J J
Unusual solid-state luminescent push-pull indolones: a general one-pot three-component approach.
Organic letters, 2010, 12, 3364-3367
1503066 CIFC30 H29 Cl3 N2 O5 SP -19.8525; 12.4298; 13.0648
71.504; 77.486; 75.275		1451.26D'Souza, Daniel M; Muschelknautz, Christian; Rominger, Frank; Müller, Thomas J J
Unusual solid-state luminescent push-pull indolones: a general one-pot three-component approach.
Organic letters, 2010, 12, 3364-3367
1503067 CIFC19 H20 N2 O5P 21 21 219.682; 9.9137; 19.0085
90; 90; 90		1824.52Xu, Yingjie; Matsunaga, Shigeki; Shibasaki, Masakatsu
syn-Selective catalytic asymmetric 1,4-addition of alpha-ketoanilides to nitroalkenes under dinuclear nickel catalysis.
Organic letters, 2010, 12, 3246-3249
1503068 CIFC14 H15 Br OP 1 21 16.24; 7.706; 12.861
90; 98.015; 90		612.4Yang, Hua; Carter, Rich G.
Synthesis of all-carbon, quaternary center-containing cyclohexenones through an organocatalyzed, multicomponent coupling.
Organic letters, 2010, 12, 3108-3111
1503069 CIFC19 H17 Cl OP -16.508; 10.191; 12.222
91.608; 103.611; 101.668		769.1Yang, Hua; Carter, Rich G.
Synthesis of all-carbon, quaternary center-containing cyclohexenones through an organocatalyzed, multicomponent coupling.
Organic letters, 2010, 12, 3108-3111
1503070 CIFC53 H52 Cl2 N2 O2 P2 RuP 21 21 2110.8594; 21.0813; 23.1923
90; 90; 90		5309.4Arai, Noriyoshi; Akashi, Masaya; Sugizaki, Satoshi; Ooka, Hirohito; Inoue, Tsutomu; Ohkuma, Takeshi
Asymmetric hydrogenation of bicyclic ketones catalyzed by BINAP/IPHAN-Ru(II) complex.
Organic letters, 2010, 12, 3380-3383
1503071 CIFC11.5 H14.5 B Cl1.5 N3 O2P -18.673; 10.421; 17.737
100.899; 94.817; 114.075		1413.8Ito, Hiroshi; Yumura, Kyohei; Saigo, Kazuhiko
Synthesis, characterization, and binding property of isoelectronic analogues of nucleobases, B(6)-substituted 5-aza-6-borauracils and -thymines.
Organic letters, 2010, 12, 3386-3389
1503072 CIFC12 H16 B N3 O2P -18.789; 12.196; 12.799
83.32; 86.166; 71.603		1292.3Ito, Hiroshi; Yumura, Kyohei; Saigo, Kazuhiko
Synthesis, characterization, and binding property of isoelectronic analogues of nucleobases, B(6)-substituted 5-aza-6-borauracils and -thymines.
Organic letters, 2010, 12, 3386-3389
1503073 CIFC18 H24 B Cl3 N6 O2P -18.135; 11.106; 14.144
68.629; 74.897; 77.76		1139.1Ito, Hiroshi; Yumura, Kyohei; Saigo, Kazuhiko
Synthesis, characterization, and binding property of isoelectronic analogues of nucleobases, B(6)-substituted 5-aza-6-borauracils and -thymines.
Organic letters, 2010, 12, 3386-3389
1503074 CIFC13 H25 Br2 In O2P -16.8758; 10.8208; 12.6521
108.628; 94.419; 101.34		864.64Nishimoto, Yoshihiro; Ueda, Hiroki; Inamoto, Yoshihiro; Yasuda, Makoto; Baba, Akio
Regioselective carboindation of simple alkenes with indium tribromide and ketene silyl acetals.
Organic letters, 2010, 12, 3390-3393
1503075 CIFC22 H38 Br4 In2 O4P 1 21/n 18.9488; 17.4208; 10.2343
90; 110.248; 90		1496.88Nishimoto, Yoshihiro; Ueda, Hiroki; Inamoto, Yoshihiro; Yasuda, Makoto; Baba, Akio
Regioselective carboindation of simple alkenes with indium tribromide and ketene silyl acetals.
Organic letters, 2010, 12, 3390-3393
1503076 CIFC17 H23 N OP 1 21/a 19.73374; 10.3541; 15.0615
90; 82.338; 90		1504.41Nishimoto, Yoshihiro; Ueda, Hiroki; Inamoto, Yoshihiro; Yasuda, Makoto; Baba, Akio
Regioselective carboindation of simple alkenes with indium tribromide and ketene silyl acetals.
Organic letters, 2010, 12, 3390-3393
1503077 CIFC15 H24 O3P 21 21 217.387; 11.854; 15.835
90; 90; 90		1386.6Navickas, Vaidotas; Ushakov, Dmitry B.; Maier, Martin E.; Ströbele, Markus; Meyer, H-Jürgen
Synthesis of the guaianolide ring system via cycloaddition of a bicyclic carbonyl ylide with allyl propiolate.
Organic letters, 2010, 12, 3418-3421
1503078 CIFC14 H16 O2P 1 21/n 111.6103; 9.3464; 21.5764
90; 104.928; 90		2262.33Butler, Jeffrey D.; Conrad, Wayne E.; Lodewyk, Michael W.; Fettinger, James C.; Tantillo, Dean J.; Kurth, Mark J.
Synthesis of substituted chromanones: an organocatalytic aldol/oxa-Michael reaction.
Organic letters, 2010, 12, 3410-3413
1503079 CIFC16 H22 OP 21 21 216.4749; 8.5245; 23.9058
90; 90; 90		1319.49Butler, Jeffrey D.; Conrad, Wayne E.; Lodewyk, Michael W.; Fettinger, James C.; Tantillo, Dean J.; Kurth, Mark J.
Synthesis of substituted chromanones: an organocatalytic aldol/oxa-Michael reaction.
Organic letters, 2010, 12, 3410-3413
1503080 CIFC10 H6 Cl O6 P WP 1 21 16.7284; 19.087; 10.4396
90; 94.175; 90		1337.1Mao, Yanli; Mathey, Francois
From furans to phosphinines.
Organic letters, 2010, 12, 3384-3385
1503081 CIFC20 H12 O13 P2 W2P -110.0533; 10.6263; 13.1213
66.685; 78.952; 84.021		1262.8Mao, Yanli; Mathey, Francois
From furans to phosphinines.
Organic letters, 2010, 12, 3384-3385
1503082 CIFC25 H24 F6 N2 O3P 1 21/c 115.679; 16.496; 8.969
90; 95.185; 90		2310Prosser, Anthony R.; Banning, Joseph E.; Rubina, Marina; Rubin, Michael
Formal nucleophilic substitution of bromocyclopropanes with amides en route to conformationally constrained β-amino acid derivatives.
Organic letters, 2010, 12, 3968-3971
1503083 CIFC22 H22 N2 OP 21 21 218.3995; 12.2643; 17.383
90; 90; 90		1790.7Ignatenko, Vasily A.; Deligonul, Nihal; Viswanathan, Rajesh
Branch-selective synthesis of oxindole and indene scaffolds: transition metal-controlled intramolecular aryl amidation leading to c3 reverse-prenylated oxindoles.
Organic letters, 2010, 12, 3594-3597
1503084 CIFC32 H50 N2 O4P 438.2499; 8.2499; 42.596
90; 90; 90		2899.1Yang, Yu-Rong; Lai, Zeng-Wei; Shen, Liang; Huang, Jiu-Zhong; Wu, Xing-De; Yin, Jun-Lin; Wei, Kun
Total synthesis of (-)-8-deoxyserratinine via an efficient Helquist annulation and double N-alkylation reaction.
Organic letters, 2010, 12, 3430-3433
1503085 CIFC16 H13 Br O2P 1 21 19.977; 5.5033; 13.198
90; 108.25; 90		688.2Chen, Zhengwang; Li, Jinghao; Jiang, Huanfeng; Zhu, Shifa; Li, Yibiao; Qi, Chaorong
Silver-catalyzed difunctionalization of terminal alkynes: highly regio- and stereoselective synthesis of (Z)-beta-haloenol acetates.
Organic letters, 2010, 12, 3262-3265
1503086 CIFC44 H49 Ni O PP 1 21/c 112.8408; 15.1873; 18.453
90; 97.9023; 90		3564.5Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503087 CIFC24 H26 O2P 1 21/a 110.2808; 15.2707; 12.1045
90; 95.07; 90		1892.91Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503088 CIFC24 H26 O2P 1 21/c 16.08838; 37.5923; 9.11131
90; 114.271; 90		1901.04Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503089 CIFC95 H139 Cl9 N16 O22P 21 21 221.4551; 28.4412; 8.9866
90; 90; 90		5483.7Fernandes, Carlos; Faure, Sophie; Pereira, Elisabeth; Théry, Vincent; Declerck, Valérie; Guillot, Régis; Aitken, David J.
12-Helix folding of cyclobutane beta-amino acid oligomers.
Organic letters, 2010, 12, 3606-3609
1503090 CIFC21 H12 N2 O2P 1 2/c 115.444; 7.4809; 14.862
90; 116.866; 90		1531.7Saha, Sukdeb; Ghosh, Amrita; Mahato, Prasenjit; Mishra, Sandhya; Mishra, Sanjiv K.; Suresh, E.; Das, Satyabrata; Das, Amitava
Specific recognition and sensing of CN- in sodium cyanide solution.
Organic letters, 2010, 12, 3406-3409
1503091 CIFC25 H16 Fe N2 O2P b c n27.672; 10.248; 13.417
90; 90; 90		3804.8Saha, Sukdeb; Ghosh, Amrita; Mahato, Prasenjit; Mishra, Sandhya; Mishra, Sanjiv K.; Suresh, E.; Das, Satyabrata; Das, Amitava
Specific recognition and sensing of CN- in sodium cyanide solution.
Organic letters, 2010, 12, 3406-3409
1503092 CIFC26 H22 F3 N O2 SP b c a15.2284; 17.6487; 17.8733
90; 90; 90		4803.7Minami, Yasunori; Kuniyasu, Hitoshi; Sanagawa, Atsushi; Kambe, Nobuaki
Pd-catalyzed regioselective iminothiolation of alkynes: a remarkable effect of the CF3 group of iminosulfides.
Organic letters, 2010, 12, 3744-3747
1503093 CIFC26 H24 OP 1 21 112.393; 5.8186; 14.691
90; 111.21; 90		987.6Chen, Zili; Zhang, Yu-Xin; Wang, Ya-Hui; Zhu, Li-Li; Liu, Heng; Li, Xiao-Xiao; Guo, Lin
Gold catalyzed diastereoselective cascade allylation/enyne cycloisomerization to construct densely functionalized oxygen heterocycles.
Organic letters, 2010, 12, 3468-3471
1503094 CIFC18 H20 O2P 1 21/c 123.7529; 6.5856; 17.3617
90; 90.515; 90		2715.73Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503095 CIFC18 H20 O2R -3 :H23.8832; 23.8832; 6.3231
90; 90; 120		3123.53Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503096 CIFC12 H17 Cl OP -110.9259; 11.4009; 14.825
100.201; 96.264; 115.471		1604.8Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503097 CIFC12 H17 Cl OR -3 :H22.0572; 22.0572; 11.2664
90; 90; 120		4746.97Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503098 CIFC13 H19 Cl OP 1 21/n 111.5914; 14.8542; 21.2577
90; 96.95; 90		3633.3Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503099 CIFC18 H21 Cl O2P 1 21/c 119.5539; 6.3547; 12.0615
90; 100.778; 90		1472.31Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503100 CIFC18 H21 Cl O2P b c a18.9939; 7.0672; 21.2043
90; 90; 90		2846.33Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503101 CIFC18 H22 O1.5P -16.3057; 10.0701; 11.3997
79.458; 81.737; 77.069		689.603Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503102 CIFC36 H55 Cl2 N O10P 21 21 2110.613; 10.756; 33.591
90; 90; 90		3834.5Igarashi, Yasuhiro; Kim, Youngju; In, Yasuko; Ishida, Toshimasa; Kan, Yukiko; Fujita, Tsuyoshi; Iwashita, Takashi; Tabata, Hirokazu; Onaka, Hiroyasu; Furumai, Tamotsu
Alchivemycin A, a bioactive polycyclic polyketide with an unprecedented skeleton from Streptomyces sp.
Organic letters, 2010, 12, 3402-3405
1503103 CIFC24 H23 F3 OP -19.5151; 9.9721; 10.8051
86.882; 89.898; 75.105		989.3Yang, Chun-Ming; Jeganmohan, Masilamani; Parthasarathy, Kanniyappan; Cheng, Chien-Hong
Highly selective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids: a novel route to substituted 1,3-dienes
Organic Letters, 2010, 12, 3610-3613
1503104 CIFC19 H20 O4P 15.3565; 7.6392; 10.099
76.068; 85.27; 86.338		399.308Yang, Chun-Ming; Jeganmohan, Masilamani; Parthasarathy, Kanniyappan; Cheng, Chien-Hong
Highly selective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids: a novel route to substituted 1,3-dienes
Organic Letters, 2010, 12, 3610-3613
1503105 CIFC11 H5 Cl F O2P 1 21/c 113.0998; 6.0571; 11.6096
90; 98.514; 90		911.03Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503106 CIFC58 H34 F2 O4P -19.124; 12.5563; 15.4232
108.753; 100.834; 98.211		1603.59Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503107 CIFC56 H36 F2 N2 O5C m c 2137.353; 15.704; 7.5165
90; 90; 90		4409.1Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503108 CIFC78 H45 F N3 O12 S2P -112.0725; 22.6806; 32.2434
84.168; 85.204; 74.958		8466.9Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503109 CIFC48 H54 F2 N6 O8P -18.572; 9.6617; 13.723
93.667; 92.869; 96.67		1124.6Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503110 CIFC18 H24 O5P -17.4222; 9.2295; 13.544
85; 74.87; 84.77		890Patel, Paresma R.; Boger, Dale L.
Intramolecular Diels-Alder reactions of cyclopropenone ketals.
Organic letters, 2010, 12, 3540-3543
1503111 CIFC16 H19 N O3P 1 21/c 119.271; 9.716; 17.52
90; 117.04; 90		2921.8Patel, Paresma R.; Boger, Dale L.
Intramolecular Diels-Alder reactions of cyclopropenone ketals.
Organic letters, 2010, 12, 3540-3543
1503112 CIFC30 H21 N3 O6P -18.2637; 12.0452; 13.7503
76.768; 80.817; 69.691		1244.7Jones, Ian M.; Hamilton, Andrew D.
Designed molecular switches: controlling the conformation of benzamido-diphenylacetylenes.
Organic letters, 2010, 12, 3651-3653
1503113 CIFC22 H28 Br2 O2P -19.211; 10.794; 11.994
106.031; 96.445; 112.428		1027.1Shenvi, Ryan A.; Corey, E. J.
Synthetic access to bent polycycles by cation-pi cyclization.
Organic letters, 2010, 12, 3548-3551
1503114 CIFC58 H68 Br4 O7P 1 21 119.335; 7.4272; 20.267
90; 104.272; 90		2820.6Shenvi, Ryan A.; Corey, E. J.
Synthetic access to bent polycycles by cation-pi cyclization.
Organic letters, 2010, 12, 3548-3551
1503115 CIFC24 H30 N2 O5P 1 21/n 113.6877; 9.8076; 15.7743
90; 90.763; 90		2117.4Kulyk, Svitlana; Dougherty, Jr, William G; Kassel, W. Scott; Fleming, Steven A.; Sieburth, Scott McN
Enyne [4 + 4] photocycloaddition: bridged 1,2,5-cyclooctatrienes.
Organic letters, 2010, 12, 3296-3299
1503116 CIFC23 H25 N O4 SP 21 21 218.274; 10.2749; 23.741
90; 90; 90		2018.3Li, Hongyan; Hsung, Richard P.; DeKorver, Kyle A.; Wei, Yonggang
Copper-catalyzed Ficini [2 + 2] cycloaddition of ynamides.
Organic letters, 2010, 12, 3780-3783
1503117 CIFC33 H33 Cl3 N2 O6 SP 21 21 215.7619; 19.3032; 29.1369
90; 90; 90		3240.7Li, Meiling; Dixon, Darren J.
Stereoselective spirolactam synthesis via palladium catalyzed arylative allene carbocyclization cascades.
Organic letters, 2010, 12, 3784-3787
1503118 CIFC17 H19 N O6P -18.8667; 9.048; 11.101
105.71; 98.61; 96.29		837.1Xu, Silong; Zou, Wen; Wu, Guiping; Song, Haibin; He, Zhengjie
Stereoselective synthesis of 1,2,3,4-tetrasubstituted dienes from allenoates and aldehydes: an observation of phosphine-induced chemoselectivity.
Organic letters, 2010, 12, 3556-3559
1503119 CIFC18 H22 O4P 1 21/n 114.985; 7.503; 15.386
90; 108.888; 90		1636.7Xu, Silong; Zou, Wen; Wu, Guiping; Song, Haibin; He, Zhengjie
Stereoselective synthesis of 1,2,3,4-tetrasubstituted dienes from allenoates and aldehydes: an observation of phosphine-induced chemoselectivity.
Organic letters, 2010, 12, 3556-3559
1503120 CIFC44 H78 N6 O11P 3121.328; 21.328; 29.108
90; 90; 120		11467Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503121 CIFC63 H115 N9 O17P 21 21 2112.247; 15.641; 77.051
90; 90; 90		14760Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503122 CIFC84 H151 N13 O22P 111.2535; 11.6895; 19.1693
86.46; 80.779; 87.428		2482.8Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503123 CIFC24 H24 N2 O6 SP 1 21/c 113.5739; 15.7377; 11.1867
90; 101.209; 90		2344.1Zhu, Zhi-Bin; Shi, Min
Ruthenium-catalyzed tandem ring-opening/ring-closing/cross-metathesis of 1,6-cyclopropene-ynes and olefins for the construction of the 3-pyrroline skeleton.
Organic letters, 2010, 12, 4462-4465
1503124 CIFC11 H14 N2 OP 1 21/c 18.925; 13.408; 17.122
90; 91.162; 90		2048.5Wei, Ying; Liu, Jing; Lin, Shaoxia; Ding, Hongqian; Liang, Fushun; Zhao, Baozhong
Acetoacetanilides as masked isocyanates: facile and efficient synthesis of unsymmetrically substituted ureas
Organic Letters, 2010, 12, 4220-4223
1503125 CIFC23 H20 Br N3 O4P -111.309; 11.587; 16.784
87.93; 80.536; 86.22		2164Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503126 CIFC22.66667 H19.66667 Cl2 N3 O4.66667P -114.308; 14.59; 19.733
101.072; 100.8; 110.784		3630.1Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503127 CIFC26 H20 Cl N3 O4P 1 21/c 111.9281; 10.2727; 22.909
90; 109.026; 90		2653.8Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503128 CIFC25 H25 Cl N2 O6P 1 21/c 110.6943; 25.494; 8.9322
90; 103.349; 90		2369.5Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503129 CIFC27 H29 Br N2 O7P -110.8467; 16.631; 17.796
112.348; 97.654; 105.826		2753.5Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503130 CIFC28 H25 Cl N2 O6P -110.3872; 11.3862; 11.9876
69.288; 72.049; 85.319		1261Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503131 CIFC29 H33 Cl N2 O5P -17.9609; 11.5503; 15.081
78.065; 83.794; 89.496		1348.7Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503132 CIFC28 H30 Cl2 N2 O5P -110.8157; 12.2522; 12.6256
101.082; 110.327; 109.908		1380.6Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503133 CIFC23 H22 Cl N3 O5P 1 21/c 111.156; 26.984; 11.394
90; 110.121; 90		3221Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503134 CIFC54 H58 Cl2 N6 O14P -16.207; 11.28; 19.29
90.298; 95.025; 99.589		1326.3Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503135 CIFC36 H22 O4P -19.799; 11.072; 13.689
70.157; 78.535; 70.146		1308.1Gong, Jian; Xie, Fuchun; Chen, Hong; Hu, Youhong
An efficient approach to functionalized benzo[a]xanthones through reactions of 2-methyl-3-(1-alkynyl)chromones with electron-deficient chromone-fused dienes.
Organic letters, 2010, 12, 3848-3851
1503136 CIFC35 H28 O7P -17.0113; 11.773; 17.526
88.586; 84.72; 81.072		1423Gong, Jian; Xie, Fuchun; Chen, Hong; Hu, Youhong
An efficient approach to functionalized benzo[a]xanthones through reactions of 2-methyl-3-(1-alkynyl)chromones with electron-deficient chromone-fused dienes.
Organic letters, 2010, 12, 3848-3851
1503137 CIFC13 H14 O4P c a 2111.0204; 8.2388; 12.1197
90; 90; 90		1100.41Cordes, Jens; Harms, Klaus; Koert, Ulrich
Synthesis of the isoquinocycline-pyrrolopyrrole substructure.
Organic letters, 2010, 12, 3808-3811
1503138 CIFC23.5 H35 N O5.5 SiP 1 21/n 116.3448; 7.0192; 23.9179
90; 98.978; 90		2710.4Cordes, Jens; Harms, Klaus; Koert, Ulrich
Synthesis of the isoquinocycline-pyrrolopyrrole substructure.
Organic letters, 2010, 12, 3808-3811
1503139 CIFC31 H40 N2 O5 S SiR -3 :H35.8162; 35.8162; 12.6101
90; 90; 120		14009Cordes, Jens; Harms, Klaus; Koert, Ulrich
Synthesis of the isoquinocycline-pyrrolopyrrole substructure.
Organic letters, 2010, 12, 3808-3811
1503140 CIFC12 H16.72 N2 O5.36P n m a19.0772; 6.9067; 9.685
90; 90; 90		1276.1Sanna, Elena; Martínez, Luis; Rotger, Carmen; Blasco, Salvador; González, Jorge; García-España, Enrique; Costa, Antoni
Squaramide-based reagent for selective chromogenic sensing of Cu(II) through a zwitterion radical.
Organic letters, 2010, 12, 3840-3843
1503141 CIFC14 H18 Cl3 N O6 SP 1 21/c 110.1519; 10.3366; 18.7036
90; 99.174; 90		1937.58Nörder, Anike; Herrmann, Pavel; Herdtweck, Eberhard; Bach, Thorsten
Acyclic stereocontrol in the catalytic C-H amination of benzylic methylene groups.
Organic letters, 2010, 12, 3690-3692
1503142 CIFC16 H25 Cl3 N O7 P SP 1 21/c 111.4476; 17.433; 12.0145
90; 104.311; 90		2323.28Nörder, Anike; Herrmann, Pavel; Herdtweck, Eberhard; Bach, Thorsten
Acyclic stereocontrol in the catalytic C-H amination of benzylic methylene groups.
Organic letters, 2010, 12, 3690-3692
1503143 CIFC18 H20 Cl3 N O6 S2P n a 2111.6761; 20.3879; 9.3747
90; 90; 90		2231.66Nörder, Anike; Herrmann, Pavel; Herdtweck, Eberhard; Bach, Thorsten
Acyclic stereocontrol in the catalytic C-H amination of benzylic methylene groups.
Organic letters, 2010, 12, 3690-3692
1503144 CIFC12 H15 Cl3 N2 O6 SP 1 21/c 19.1997; 19.5983; 9.8197
90; 95.769; 90		1761.51Nörder, Anike; Herrmann, Pavel; Herdtweck, Eberhard; Bach, Thorsten
Acyclic stereocontrol in the catalytic C-H amination of benzylic methylene groups.
Organic letters, 2010, 12, 3690-3692
1503145 CIFC14 H18 Cl3 N O6 SP n a 2122.6616; 6.417; 13.3006
90; 90; 90		1934.17Nörder, Anike; Herrmann, Pavel; Herdtweck, Eberhard; Bach, Thorsten
Acyclic stereocontrol in the catalytic C-H amination of benzylic methylene groups.
Organic letters, 2010, 12, 3690-3692
1503146 CIFC34 H51 F2 N4 O6P -111.595; 12.1153; 13.243
73.015; 77.927; 74.042		1693.8Zeika, Olaf; Li, Yongjun; Jockusch, Steffen; Parkin, Gerard; Sattler, Aaron; Sattler, Wesley; Turro, Nicholas J.
Synthesis of polynitroxides based on nucleophilic aromatic substitution.
Organic letters, 2010, 12, 3696-3699
1503147 CIFC16 H17 F4 N2 O2P 21 21 2110.7868; 11.377; 12.9981
90; 90; 90		1595.15Zeika, Olaf; Li, Yongjun; Jockusch, Steffen; Parkin, Gerard; Sattler, Aaron; Sattler, Wesley; Turro, Nicholas J.
Synthesis of polynitroxides based on nucleophilic aromatic substitution.
Organic letters, 2010, 12, 3696-3699
1503148 CIFC25 H34 F3 N3 O4P 1 21/n 116.1428; 7.6731; 20.8194
90; 98.721; 90		2549Zeika, Olaf; Li, Yongjun; Jockusch, Steffen; Parkin, Gerard; Sattler, Aaron; Sattler, Wesley; Turro, Nicholas J.
Synthesis of polynitroxides based on nucleophilic aromatic substitution.
Organic letters, 2010, 12, 3696-3699
1503149 CIFC42 H68 N6 O8C 1 2/c 128.068; 11.6716; 16.1222
90; 124.007; 90		4378.3Zeika, Olaf; Li, Yongjun; Jockusch, Steffen; Parkin, Gerard; Sattler, Aaron; Sattler, Wesley; Turro, Nicholas J.
Synthesis of polynitroxides based on nucleophilic aromatic substitution.
Organic letters, 2010, 12, 3696-3699
1503150 CIFC17 H15 Br O2P 21 21 216.8149; 14.637; 14.679
90; 90; 90		1464.2Shao, Cheng; Yu, Hong-Jie; Wu, Nuo-Yi; Feng, Chen-Guo; Lin, Guo-Qiang
C1-symmetric dicyclopentadienes as new chiral diene ligands for asymmetric rhodium-catalyzed arylation of N-tosylarylimines.
Organic letters, 2010, 12, 3820-3823
1503151 CIFC18 H15 Br O2P 1 21 113.5681; 8.1292; 15.1521
90; 107.156; 90		1596.88Yu, Jie; Chen, Wei-Jie; Gong, Liu-Zhu
Kinetic resolution of racemic 2,3-allenoates by organocatalytic asymmetric 1,3-dipolar cycloaddition.
Organic letters, 2010, 12, 4050-4053
1503152 CIFC16 H12 N2 O0 SC 1 2/c 119.0234; 10.3429; 14.4289
90; 112.754; 90		2618Xu, Hui; Zhang, Yin; Huang, Jianqiang; Chen, Wanzhi
Copper-catalyzed synthesis of N-fused heterocycles through regioselective 1,2-aminothiolation of 1,1-dibromoalkenes.
Organic letters, 2010, 12, 3704-3707
1503153 CIFC17 H23 Br N2 O0 SP 1 21/n 18.7689; 24.7018; 9.0693
90; 112.788; 90		1811.14Xu, Hui; Zhang, Yin; Huang, Jianqiang; Chen, Wanzhi
Copper-catalyzed synthesis of N-fused heterocycles through regioselective 1,2-aminothiolation of 1,1-dibromoalkenes.
Organic letters, 2010, 12, 3704-3707
1503154 CIFC14 H11 Cl N2 OP -15.7679; 8.2804; 12.9064
74.09; 88.512; 85.529		590.99Urgaonkar, Sameer; Cortese, Joseph F.; Barker, Robert H.; Cromwell, Mandy; Serrano, Adelfa E.; Wirth, Dyann F.; Clardy, Jon; Mazitschek, Ralph
A concise silylamine approach to 2-amino-3-hydroxy-indoles with potent in vivo antimalaria activity.
Organic letters, 2010, 12, 3998-4001
1503155 CIFC42 H37 N4 Ni O4P 21 21 2111.937; 14.935; 19.399
90; 90; 90		3458.4Dong, Zhenzhen; Plampin, 3rd, James N; Yap, Glenn P. A.; Fox, Joseph M.
Minimalist end groups for control of absolute helicity in salen- and salophen-based metallofoldamers.
Organic letters, 2010, 12, 4002-4005
1503156 CIFC43 H44 Cl2 N4 Ni O4P 112.3092; 12.3128; 12.973
90.061; 102.664; 98.557		1895.9Dong, Zhenzhen; Plampin, 3rd, James N; Yap, Glenn P. A.; Fox, Joseph M.
Minimalist end groups for control of absolute helicity in salen- and salophen-based metallofoldamers.
Organic letters, 2010, 12, 4002-4005
1503157 CIFC21 H33 N3 O5 S SiP 1 21 17.6795; 8.1287; 21.2564
90; 99.965; 90		1306.9Kelley, Brandon T.; Joullié, Madeleine M
Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
Organic letters, 2010, 12, 4244-4247
1503158 CIFC22 H35 N3 O6 S SiC 1 2 131.131; 7.805; 22.844
90; 110.163; 90		5210.4Kelley, Brandon T.; Joullié, Madeleine M
Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
Organic letters, 2010, 12, 4244-4247
1503159 CIFC19 H28 N2 O5 S SiP 1 21 17.2155; 7.3686; 21.8244
90; 91.207; 90		1160.11Kelley, Brandon T.; Joullié, Madeleine M
Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
Organic letters, 2010, 12, 4244-4247
1503160 CIFC26 H22 N2 O4P 1 21/c 110.513; 21.209; 19.5593
90; 90.309; 90		4361.1Gao, Meng; Yang, Yan; Wu, Yan-Dong; Deng, Cong; Shu, Wen-Ming; Zhang, Dong-Xue; Cao, Li-Ping; She, Neng-Fang; Wu, An-Xin
An efficient synthesis of hydantoins via sustainable integration of coupled domino processes.
Organic letters, 2010, 12, 4026-4029
1503161 CIFC27 H23 N2 O4.5P b c n11.301; 17.774; 22.517
90; 90; 90		4522.9Gao, Meng; Yang, Yan; Wu, Yan-Dong; Deng, Cong; Shu, Wen-Ming; Zhang, Dong-Xue; Cao, Li-Ping; She, Neng-Fang; Wu, An-Xin
An efficient synthesis of hydantoins via sustainable integration of coupled domino processes.
Organic letters, 2010, 12, 4026-4029
1503162 CIFC124 H106 N8 O9P 1 21 120.312; 9.5308; 26.2849
90; 107.355; 90		4856.8Wiedner, Susan D.; Vedejs, Edwin
Aziridinomitosanes via lactam cyclization.
Organic letters, 2010, 12, 4030-4033
1503163 CIFC46 H45 N2 O7.5P 21 21 2112.8063; 13.3599; 48.7876
90; 90; 90		8347.1Wiedner, Susan D.; Vedejs, Edwin
Aziridinomitosanes via lactam cyclization.
Organic letters, 2010, 12, 4030-4033
1503164 CIFC32 H50 N6 O2P -16.897; 11.772; 20.837
78.683; 88.669; 73.136		1586.5Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish
Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions.
Organic letters, 2010, 12, 3910-3913
1503165 CIFC32 H48 N6 O4 SC m c 2117.106; 16.317; 11.461
90; 90; 90		3199Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish
Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions.
Organic letters, 2010, 12, 3910-3913
1503166 CIFC28 H42 N4 O7 SP 1 21/c 119.123; 13.758; 11.749
90; 106.098; 90		2969.9Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish
Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions.
Organic letters, 2010, 12, 3910-3913
1503167 CIFC17 H25 N O3P 21 21 219.1204; 11.6853; 14.1079
90; 90; 90		1503.54Zhao, Fu-Wei; Sun, Qian-Yun; Yang, Fu-Mei; Hu, Guang-Wan; Luo, Ji-Feng; Tang, Gui-Hua; Wang, Yue-Hu; Long, Chun-Lin
Palhinine A, a novel alkaloid from Palhinhaea cernua.
Organic letters, 2010, 12, 3922-3925
1503168 CIFC24 H24 N2 O4P -19.941; 10.774; 11.867
77.103; 66.061; 65.409		1054McCormack, Michael P.; Shalumova, Tamila; Tanski, Joseph M.; Waters, Stephen P.
Development of a 2-aza-Cope-[3 + 2] dipolar cycloaddition strategy for the synthesis of quaternary proline scaffolds.
Organic letters, 2010, 12, 3906-3909
1503169 CIFC23 H19 N O2P -18.0436; 10.604; 11.289
110.89; 95.92; 99.62		873Yang, Luo; Lei, Chuan-Hu; Wang, De-Xian; Huang, Zhi-Tang; Wang, Mei-Xiang
Highly efficient and expedient synthesis of 5-hydroxy-1H-pyrrol-2-(5H)-ones from FeCl3-catalyzed tandem intramolecular enaminic addition of tertiary enamides to ketones and 1,3-hydroxy rearrangement.
Organic letters, 2010, 12, 3918-3921
1503170 CIFC24 H21 N O2P 1 21/c 18.5467; 10.49; 21.228
90; 101.57; 90		1864.5Yang, Luo; Lei, Chuan-Hu; Wang, De-Xian; Huang, Zhi-Tang; Wang, Mei-Xiang
Highly efficient and expedient synthesis of 5-hydroxy-1H-pyrrol-2-(5H)-ones from FeCl3-catalyzed tandem intramolecular enaminic addition of tertiary enamides to ketones and 1,3-hydroxy rearrangement.
Organic letters, 2010, 12, 3918-3921
1503171 CIFC25 H23 Br N O3 P SP 1 21/c 19.276; 22.735; 11.894
90; 110.871; 90		2343.7Xie, Peizhong; Huang, You; Chen, Ruyu
Phosphine-catalyzed domino reaction: highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allylic carbonates.
Organic letters, 2010, 12, 3768-3771
1503172 CIFC31 H27 Br N O3 P SP 21 21 2110.26; 8.486; 30.754
90; 90; 90		2677.6Xie, Peizhong; Huang, You; Chen, Ruyu
Phosphine-catalyzed domino reaction: highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allylic carbonates.
Organic letters, 2010, 12, 3768-3771
1503173 CIFC13 H7 B F5 N3P 1 21/c 18.39; 28.706; 20.46
90; 93.631; 90		4918Kubota, Yasuhiro; Tsuzuki, Toshihiro; Funabiki, Kazumasa; Ebihara, Masahiro; Matsui, Masaki
Synthesis and fluorescence properties of a pyridomethene-BF2 complex.
Organic letters, 2010, 12, 4010-4013
1503174 CIFC12 H8 B F2 N3P 1 21/c 16.855; 18.051; 17.675
90; 100.818; 90		2148.2Kubota, Yasuhiro; Tsuzuki, Toshihiro; Funabiki, Kazumasa; Ebihara, Masahiro; Matsui, Masaki
Synthesis and fluorescence properties of a pyridomethene-BF2 complex.
Organic letters, 2010, 12, 4010-4013
1503175 CIFC16 H19 N O S2P 1 21/c 18.07; 10.917; 17.772
90; 90.891; 90		1565.5Evenson, Sean J.; Rasmussen, Seth C.
N-acyldithieno[3,2-b:2',3'-d]pyrroles: second generation dithieno[3,2-b:2',3'-d]pyrrole building blocks with stabilized energy levels.
Organic letters, 2010, 12, 4054-4057
1503176 CIFC15 H9 N O S2P 1 21/c 111.802; 11.154; 10.384
90; 109.858; 90		1285.7Evenson, Sean J.; Rasmussen, Seth C.
N-acyldithieno[3,2-b:2',3'-d]pyrroles: second generation dithieno[3,2-b:2',3'-d]pyrrole building blocks with stabilized energy levels.
Organic letters, 2010, 12, 4054-4057
1503177 CIFC15 H15 N O S2P -18.321; 8.994; 9.073
95.102; 93.093; 92.926		674.3Evenson, Sean J.; Rasmussen, Seth C.
N-acyldithieno[3,2-b:2',3'-d]pyrroles: second generation dithieno[3,2-b:2',3'-d]pyrrole building blocks with stabilized energy levels.
Organic letters, 2010, 12, 4054-4057
1503178 CIFC18 H19 Br N2 OC 1 2 118.7232; 6.9539; 14.145
90; 120.22; 90		1591.39Holloway, Chloe A.; Muratore, Michael E.; Storer, R. Lan; Dixon, Darren J.
Direct enantioselective Brønsted acid catalyzed N-acyliminium cyclization cascades of tryptamines and ketoacids.
Organic letters, 2010, 12, 4720-4723
1503179 CIFC17 H20 N2 OP 1 21/n 15.7927; 12.1783; 20.5935
90; 94.4916; 90		1448.31Holloway, Chloe A.; Muratore, Michael E.; Storer, R. Lan; Dixon, Darren J.
Direct enantioselective Brønsted acid catalyzed N-acyliminium cyclization cascades of tryptamines and ketoacids.
Organic letters, 2010, 12, 4720-4723
1503180 CIFC20 H35 Cl O2 SiP 1 21/a 19.956; 20.04; 11.392
90; 109.09; 90		2148Matsuo, Jun-ichi; Kawano, Mizuki; Okuno, Ryosuke; Ishibashi, Hiroyuki
Titanium(IV) chloride-mediated carbon-carbon bond-forming reaction between 3,3-dialkylcyclobutanones and aldehydes.
Organic letters, 2010, 12, 3960-3962
1503181 CIFC17 H25 N O5P 1 21/n 111.4665; 7.9203; 19.816
90; 95.306; 90		1791.9An, Guanghui; Zhou, Wei; Zhang, Guangqian; Sun, Hao; Han, Jianlin; Pan, Yi
Palladium-catalyzed tandem diperoxidation/C-H activation resulting in diperoxy-oxindole in air.
Organic letters, 2010, 12, 4482-4485
1503182 CIFC29 H25 N3 O5 SP 21 21 2110.6109; 11.3274; 22.798
90; 90; 90		2740.2Peng, Jing; Huang, Xin; Cui, Hai-Lei; Chen, Ying-Chun
Organocatalytic and electrophilic approach to oxindoles with C3-quaternary stereocenters.
Organic letters, 2010, 12, 4260-4263
1503183 CIFC53 H34 F6 O2 S2P -112.4284; 13.7209; 13.789
95.204; 108.784; 101.21		2153.8Delbaere, Stéphanie; Vermeersch, Gaston; Frigoli, Michel; Mehl, Georg H.
Bridging the visible: the modulation of the absorption by more than 450 nm.
Organic letters, 2010, 12, 4090-4093
1503184 CIFC21 H21 N O2 SP 21 21 214.5421; 10.033; 37.818
90; 90; 90		1723.4Sabala, Rocío; Hernández-García, Luis; Ortiz, Aurelio; Romero, Moisés; Olivo, Horacio F.
Diastereoselective conjugate addition of organocuprates to chiral N-enoyl oxazolidinethiones.
Organic letters, 2010, 12, 4268-4270
1503185 CIFC22 H25 N O2 SP 1 21 15.437; 16.067; 11.335
90; 96.72; 90		983.4Sabala, Rocío; Hernández-García, Luis; Ortiz, Aurelio; Romero, Moisés; Olivo, Horacio F.
Diastereoselective conjugate addition of organocuprates to chiral N-enoyl oxazolidinethiones.
Organic letters, 2010, 12, 4268-4270
1503186 CIFC30 H28 B Cl2 F N2 OP b c a15.361; 14.451; 23.729
90; 90; 90		5267Shintani, Ryo; Soh, Ying-Teck; Hayashi, Tamio
Rhodium-catalyzed asymmetric arylation of azomethine imines.
Organic letters, 2010, 12, 4106-4109
1503187 CIFC16 H15 Cl N2 OP 1 21 19.71; 16.275; 17.801
90; 92.955; 90		2809.4Shintani, Ryo; Soh, Ying-Teck; Hayashi, Tamio
Rhodium-catalyzed asymmetric arylation of azomethine imines.
Organic letters, 2010, 12, 4106-4109
1503188 CIFC22 H19 F N2 OP 1 21/a 110.266; 16.834; 11.491
90; 114.101; 90		1812.7Shintani, Ryo; Soh, Ying-Teck; Hayashi, Tamio
Rhodium-catalyzed asymmetric arylation of azomethine imines.
Organic letters, 2010, 12, 4106-4109
1503189 CIFC23 H15 N OP 1 21/c 110.1003; 17.6993; 10.2661
90; 115.709; 90		1653.58Schönhaber, Jan; Frank, Walter; Müller, Thomas J J
Insertion-coupling-cycloisomerization domino synthesis and cation-induced halochromic fluorescence of 2,4-diarylpyrano[2,3-b]indoles.
Organic letters, 2010, 12, 4122-4125
1503190 CIFC75 H63 Cl9 O2P -110.293; 15.245; 21.665
87.02; 86.029; 79.479		3331.7Zhang, Xiaojie; Li, Jinling; Qu, Hemi; Chi, Chunyan; Wu, Jishan
Fused bispentacenequinone and its unexpected Michael addition.
Organic letters, 2010, 12, 3946-3949
1503191 CIFC11 H8 O4P 1 21/c 17.112; 15.443; 8.5355
90; 102.864; 90		913.9Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503192 CIFC12 H10 O4P 1 21/n 14.6951; 9.7328; 22.307
90; 94.848; 90		1015.7Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503193 CIFC13 H12 O4P 1 21/c 18.0748; 9.2016; 15.5271
90; 100.084; 90		1135.86Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503194 CIFC22 H16 O8P -19.128; 10.3355; 10.6415
76.61; 68.814; 82.929		909.78Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503195 CIFC24 H20 O8C 1 2/c 111.4827; 11.0568; 16.4519
90; 106.924; 90		1998.3Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503196 CIFC26 H24 O8P 16.5748; 8.8652; 10.7627
69.163; 82.406; 82.35		578.64Sakamoto, Masami; Yagishita, Fumitoshi; Kanehiro, Masayuki; Kasashima, Yoshio; Mino, Takashi; Fujita, Tsutomu
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.
Organic letters, 2010, 12, 4435-4437
1503197 CIFC17 H19 N O5P c a b8.2353; 13.2297; 28.508
90; 90; 90		3106Miege, Frédéric; Meyer, Christophe; Cossy, Janine
Synthesis of 3-oxa- and 3-azabicyclo[4.1.0]heptanes by gold-catalyzed cycloisomerization of cyclopropenes.
Organic letters, 2010, 12, 4144-4147
1503198 CIFC29 H26 N8 O11P 1 21/n 115.196; 11.833; 16.715
90; 107.475; 90		2866.9Katz, Jeffrey L.; Tschaen, Brittany A.
Synthesis of inherently chiral azacalix[4]arenes and diazadioxacalix[4]arenes.
Organic letters, 2010, 12, 4300-4303
1503199 CIFC28 H18 B N3 O S3P -17.504; 13.407; 13.408
110.09; 104; 104.77		1141.5Hayashi, Shin-ya; Inokuma, Yasuhide; Osuka, Atsuhiro
meso-Tris(oligo-2,5-thienylene)-substituted subporphyrins.
Organic letters, 2010, 12, 4148-4151
1503200 CIFC28 H15 B Br3 N3 O S3C 1 2/c 128.04; 7.483; 26.42
90; 101.36; 90		5435Hayashi, Shin-ya; Inokuma, Yasuhide; Osuka, Atsuhiro
meso-Tris(oligo-2,5-thienylene)-substituted subporphyrins.
Organic letters, 2010, 12, 4148-4151
1503201 CIFC52 H30 B N3 O S9P -114.9; 18.725; 19.242
113.171; 111.245; 95.232		4426Hayashi, Shin-ya; Inokuma, Yasuhide; Osuka, Atsuhiro
meso-Tris(oligo-2,5-thienylene)-substituted subporphyrins.
Organic letters, 2010, 12, 4148-4151
1503202 CIFC21 H18 Br F3 O3P -19.156; 10.791; 20.165
86.746; 84.069; 79.233		1945.4Wang, Tong; Ye, Song
Diastereoselective synthesis of 6-trifluoromethyl-5,6-dihydropyrans via phosphine-catalyzed [4 + 2] annulation of α-benzylallenoates with ketones.
Organic letters, 2010, 12, 4168-4171
1503203 CIFC12 H9 Cl O2P b c a15.103; 6.0078; 21.747
90; 90; 90		1973.2Huo, Fang-Jun; Sun, Yuan-Qiang; Su, Jing; Yang, Yu-Tao; Yin, Cai-Xia; Chao, Jian-Bin
Chromene "lock", thiol "key", and mercury(II) ion "hand": a single molecular machine recognition system.
Organic letters, 2010, 12, 4756-4759
1503204 CIFC94 H74.44 Cl2 N8 O0.22P -110.676; 18.951; 19.394
85.406; 74.527; 74.304		3640.5Hatano, Sayaka; Sakai, Ken; Abe, Jiro
Unprecedented radical-radical reaction of a [2.2]paracyclophane derivative containing an imidazolyl radical moiety.
Organic letters, 2010, 12, 4152-4155
1503205 CIFC20 H25 Br2 N O4P 21 21 216.6549; 13.8696; 21.4953
90; 90; 90		1984Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
Tetraquinanes via [4 + 4] photocycloaddition/transannular ring closure.
Organic letters, 2010, 12, 4510-4512
1503206 CIFC20 H27 N O5P 21 21 217.4039; 13.4534; 17.6386
90; 90; 90		1756.9Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
Tetraquinanes via [4 + 4] photocycloaddition/transannular ring closure.
Organic letters, 2010, 12, 4510-4512
1503207 CIFC10 H10 Br2 Cl3 N O2P 21 21 218.573; 9.9838; 16.5361
90; 90; 90		1415.34Bae, Ju-Yeon; Lee, Hyo-Jun; Youn, Seok-Ho; Kwon, Su-Hyun; Cho, Chang-Woo
Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions.
Organic letters, 2010, 12, 4352-4355
1503208 CIFC18 H20 O2P b c a9.9559; 13.4641; 21.4149
90; 90; 90		2870.61Ramadhar, Timothy R.; Kawakami, Jun-ichi; Lough, Alan J.; Batey, Robert A.
Stereocontrolled synthesis of contiguous C(sp3)-C(aryl) bonds by lanthanide(III)-catalyzed domino aryl-Claisen [3,3]-sigmatropic rearrangements.
Organic letters, 2010, 12, 4446-4449
1503209 CIFC18 H16 N2 O6C 1 2/c 116.3276; 9.2926; 11.4092
90; 108.846; 90		1638.27Ramadhar, Timothy R.; Kawakami, Jun-ichi; Lough, Alan J.; Batey, Robert A.
Stereocontrolled synthesis of contiguous C(sp3)-C(aryl) bonds by lanthanide(III)-catalyzed domino aryl-Claisen [3,3]-sigmatropic rearrangements.
Organic letters, 2010, 12, 4446-4449
1503210 CIFC22 H27 Br O5P -19.745; 10.404; 11.659
69.894; 67.4; 87.178		1020.1Jones, Brian D.; La Clair, James J.; Moore, Curtis E.; Rheingold, Arnold L.; Burkart, Michael D.
Convergent route to the spirohexenolide macrocycle.
Organic letters, 2010, 12, 4516-4519
1503211 CIFC26 H32 O5P 1 21/c 120.834; 12.224; 8.784
90; 93.811; 90		2232.1Jones, Brian D.; La Clair, James J.; Moore, Curtis E.; Rheingold, Arnold L.; Burkart, Michael D.
Convergent route to the spirohexenolide macrocycle.
Organic letters, 2010, 12, 4516-4519
1503212 CIFC14 H8 N2 SP 1 21/n 13.8045; 14.624; 18.5827
90; 92.86; 90		1032.6Linder, Thomas; Badiola, Eider; Baumgartner, Thomas; Sutherland, Todd C.
Synthesis of π-extended thiadiazole (oxides) and their electronic properties.
Organic letters, 2010, 12, 4520-4523
1503213 CIFC14 H8 N2 O2 SP 1 21/c 16.9578; 17.055; 10.133
90; 112.64; 90		1109.8Linder, Thomas; Badiola, Eider; Baumgartner, Thomas; Sutherland, Todd C.
Synthesis of π-extended thiadiazole (oxides) and their electronic properties.
Organic letters, 2010, 12, 4520-4523
1503214 CIFC16 H8 N2 SP 1 21/c 117.1841; 3.8524; 34.3919
90; 95.801; 90		2265.1Linder, Thomas; Badiola, Eider; Baumgartner, Thomas; Sutherland, Todd C.
Synthesis of π-extended thiadiazole (oxides) and their electronic properties.
Organic letters, 2010, 12, 4520-4523
1503215 CIFC16 H8 N2 O SC 1 2/c 114.6637; 11.904; 7.2169
90; 115.913; 90		1133.1Linder, Thomas; Badiola, Eider; Baumgartner, Thomas; Sutherland, Todd C.
Synthesis of π-extended thiadiazole (oxides) and their electronic properties.
Organic letters, 2010, 12, 4520-4523
1503216 CIFC16 H8 N2 O2 SP 1 21/c 111.4588; 15.8146; 6.8807
90; 102.5; 90		1217.34Linder, Thomas; Badiola, Eider; Baumgartner, Thomas; Sutherland, Todd C.
Synthesis of π-extended thiadiazole (oxides) and their electronic properties.
Organic letters, 2010, 12, 4520-4523
1503217 CIFC21 H18 Br2 N4 O SP -17.63; 11.254; 12.992
104.415; 104.272; 99.48		1016.3Feldman, Ken S.; Nuriye, Ahmed Yimam
Extending Pummerer reaction chemistry: application to the assembly of the pentacyclic core of dibromopalau'amine.
Organic letters, 2010, 12, 4532-4535
1503218 CIFC78 H110 Cl2 N O10F d d 255.9475; 44.3294; 12.4822
90; 90; 90		30957.3Han, Chengyou; Ma, Fengying; Zhang, Zibin; Xia, Binyuan; Yu, Yihua; Huang, Feihe
DIBPillar[n]arenes (n = 5, 6): syntheses, X-ray crystal structures, and complexation with n-octyltriethyl ammonium hexafluorophosphate.
Organic letters, 2010, 12, 4360-4363
1503219 CIFC189 H264 N4 O24P -113.7506; 18.3037; 19.5207
78.89; 78.46; 78.098		4651.17Han, Chengyou; Ma, Fengying; Zhang, Zibin; Xia, Binyuan; Yu, Yihua; Huang, Feihe
DIBPillar[n]arenes (n = 5, 6): syntheses, X-ray crystal structures, and complexation with n-octyltriethyl ammonium hexafluorophosphate.
Organic letters, 2010, 12, 4360-4363
1503220 CIFC20 H22 N2 O2P 1 21/c 19.174; 17.881; 10.373
90; 97.844; 90		1685.7Fujiwara, Kyohei; Kurahashi, Takuya; Matsubara, Seijiro
Decarbonylative cycloaddition of phthalimides with 1,3-dienes.
Organic letters, 2010, 12, 4548-4551
1503221 CIFC21 H25 N3 OP 1 21/c 19.6129; 15.9; 12.4424
90; 109.191; 90		1796.1Fujiwara, Kyohei; Kurahashi, Takuya; Matsubara, Seijiro
Decarbonylative cycloaddition of phthalimides with 1,3-dienes.
Organic letters, 2010, 12, 4548-4551
1503222 CIFC19 H21 N3 OP -110.6196; 11.847; 13.843
91.696; 104.085; 97.966		1669.3Fujiwara, Kyohei; Kurahashi, Takuya; Matsubara, Seijiro
Decarbonylative cycloaddition of phthalimides with 1,3-dienes.
Organic letters, 2010, 12, 4548-4551
1503223 CIFC38 H34 O4P -17.272; 12.692; 17.264
97.762; 100.795; 101.825		1506.9An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503224 CIFC42 H42 O4P 1 21/n 122.952; 7.0269; 23.009
90; 112.606; 90		3425.8An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503225 CIFC50 H58 O4P 1 21/c 115.644; 29.507; 9.359
90; 92.468; 90		4316An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503226 CIFC54 H66 O4P -19.1618; 15.607; 17.154
101.382; 91.325; 92.182		2401.7An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503227 CIFC29 H37 O2P -15.8496; 14.2422; 15.3416
92.896; 98.283; 98.842		1246.31An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503228 CIFC62 H77 O4P -19.247; 15.35; 19.998
78.927; 87.884; 86.674		2780An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503229 CIFC46 H50 O4P -112.763; 13.447; 14.34
65.731; 66.619; 62.46		1923.2An, Peng; Shi, Zi-Fa; Dou, Wei; Cao, Xiao-Ping; Zhang, Hao-Li
Synthesis of 1,4-bis[2,2-bis(4-alkoxyphenyl)vinyl]benzenes and side chain modulation of their solid-state emission.
Organic letters, 2010, 12, 4364-4367
1503230 CIFC15 H17 N O4P -16.999; 12.277; 17.34
93.43; 91.45; 106.06		1428Seraya, Elaine; Slack, Eric; Ariafard, Alireza; Yates, Brian F.; Hyland, Christopher J. T.
Experimental and theoretical investigation into the gold-catalyzed reactivity of cyclopropenylmethyl acetates.
Organic letters, 2010, 12, 4768-4771
1503231 CIFC29 H46 N4 O3P n a 2116.092; 13.971; 12.527
90; 90; 90		2816.34Escudero-Adán, Eduardo C; Martínez Belmonte, Marta; Benet-Buchholz, Jordi; Kleij, Arjan W.
Practical approach to structurally diverse monoimine salts and nonsymmetrical metallosalphen complexes.
Organic letters, 2010, 12, 4592-4595
1503232 CIFC29 H44 Cl2 N4 O3P n a 2116.1444; 14.8471; 12.468
90; 90; 90		2988.5Escudero-Adán, Eduardo C; Martínez Belmonte, Marta; Benet-Buchholz, Jordi; Kleij, Arjan W.
Practical approach to structurally diverse monoimine salts and nonsymmetrical metallosalphen complexes.
Organic letters, 2010, 12, 4592-4595
1503233 CIFC29 H45 Br2 N3 OP n a 2115.8418; 14.3022; 13.0883
90; 90; 90		2965.5Escudero-Adán, Eduardo C; Martínez Belmonte, Marta; Benet-Buchholz, Jordi; Kleij, Arjan W.
Practical approach to structurally diverse monoimine salts and nonsymmetrical metallosalphen complexes.
Organic letters, 2010, 12, 4592-4595

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