The Ugi five-component condensation using CO2, CS2, and COS as oxidized carbon sources

被引:48
作者
Keating, TA [1 ]
Armstrong, RW [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
关键词
D O I
10.1021/jo971463z
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:867 / 871
页数:5
相关论文
共 15 条
[1]  
[Anonymous], ANGEW CHEM INT EDIT, DOI DOI 10.1002/ANIE.199622881
[2]  
Armstrong Robert W., 1997, P153
[3]   Multiple-component condensation strategies for combinatorial library synthesis [J].
Armstrong, RW ;
Combs, AP ;
Tempest, PA ;
Brown, SD ;
Keating, TA .
ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (03) :123-131
[4]  
Dunn A. D., 1989, CARBON DISULPHIDE OR, P226
[5]  
HILDEBRAND JH, 1950, SOLUBILITY NONELECTR, P248
[6]   A remarkable two-step synthesis of diverse 1,4-benzodiazepine-2,5-diones using the Ugi four-component condensation [J].
Keating, TA ;
Armstrong, RW .
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (25) :8935-8939
[7]   MOLECULAR DIVERSITY VIA A CONVERTIBLE ISOCYANIDE IN THE UGI 4-COMPONENT CONDENSATION [J].
KEATING, TA ;
ARMSTRONG, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (29) :7842-7843
[8]   Postcondensation modifications of Ugi four-component condensation products: 1-Isocyanocyclohexene as a convertible isocyanide. Mechanism of conversion, synthesis of diverse structures, and demonstration of resin capture [J].
Keating, TA ;
Armstrong, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (11) :2574-2583
[9]   Solid phase synthesis of pyrroles derived from a four component condensation [J].
Mjalli, AMM ;
Sarshar, S ;
Baiga, TJ .
TETRAHEDRON LETTERS, 1996, 37 (17) :2943-2946
[10]   Use of a convertible isocyanide for generation of Ugi reaction derivatives on solid support: Synthesis of alpha-acylaminoesters and pyrroles [J].
Strocker, AM ;
Keating, TA ;
Tempest, PA ;
Armstrong, RW .
TETRAHEDRON LETTERS, 1996, 37 (08) :1149-1152