Synthesis of natural products via stereocontrolled palladium-catalyzed reactions

被引:13
作者
Bäckvall, JE [1 ]
机构
[1] Stockholm Univ, Arrhenius Lab, Dept Organ Chem, SE-10691 Stockholm, Sweden
关键词
D O I
10.1351/pac199971061065
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stereocontrolled palladium-catalyzed reactions were employed in the stereoselective synthesis of some natural products. Thus (+/-)-epibatidine (-) paeonilactone A (and B), and (-)-conduritol C, and (+)-monomorine I were synthesized.
引用
收藏
页码:1065 / 1070
页数:6
相关论文
共 18 条
[1]  
ANDERSSON PG, 1996, ADV HET NAT, V3, P179
[2]  
BACKVALL JE, 1993, SYNTHESIS-STUTTGART, P343
[3]  
Backvall JE, 1998, METAL-CATALYZED CROSS-COUPLING REACTIONS, P339
[4]  
BACKVALL JE, 1995, STUD NAT PROD CHEM, V16, P415
[5]  
BROKA CA, 1994, MED CHEM RES, V4, P449
[6]  
FUJIWARA M, 1990, JPN J NEUROPSYCHOPH, V12, P217
[7]  
Harrington P.M., 1995, Comprehensive Organometallic Chemistry II, V12, P797
[8]   PAEONILACTONE-A, PAEONILACTONE-B, AND PAEONILACTONE-C, NEW MONOTERPENOIDS FROM PAEONY ROOT [J].
HAYASHI, T ;
SHINBO, T ;
SHIMIZU, M ;
ARISAWA, M ;
MORITA, N ;
KIMURA, M ;
MATSUDA, S ;
KIKUCHI, T .
TETRAHEDRON LETTERS, 1985, 26 (31) :3699-3702
[9]  
KADOTA S, 1989, CHEM PHARM BULL, V3, P843
[10]   A versatile route to 2-substituted cyclic 1,3-dienes via a copper(I)-catalyzed cross-coupling reaction of dienyl triflates with Grignard reagents [J].
Karlström, ASE ;
Rönn, M ;
Thorarensen, A ;
Bäckvall, JE .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (08) :2517-2522