Recent progress in the chemistry of the monoterpenoid indole alkaloids

被引：215
作者：
Saxton, JE
机构：
[1] School of Chemistry, University of Leeds
来源：
NATURAL PRODUCT REPORTS | 1997年 / 14卷 / 06期
关键词：
D O I：
10.1039/np9971400559
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
[No abstract available]
引用
收藏
页码：559 / 590
页数：32
相关论文
共 149 条
[1]  
Aimi N, 1996, CHEM PHARM BULL, V44, P1637, DOI 10.1248/cpb.44.1637
[2]  
AKIMOTO K, 1996, DRUG STABILITY, V1, P118
[3]  
Amann R, 1996, LIEBIGS ANN, P349
[4]   An enantioselective synthesis of the Strychnos alkaloid (-)-tubifoline [J].
Amat, M ;
Coll, MD ;
Passarella, D ;
Bosch, J .
TETRAHEDRON-ASYMMETRY, 1996, 7 (10) :2775-2778
[5]   A new synthetic entry to the indolo[2,3-a]quinolizidine system. Electrophilic cyclizations on the indole ring from 2-(2-piperidyl)indoles [J].
Amat, M ;
Hadida, S ;
Sathyanarayana, S ;
Bosch, J .
TETRAHEDRON LETTERS, 1996, 37 (17) :3071-3074
[6]  
Angiolini L, 1996, GAZZ CHIM ITAL, V126, P69
[7]   Enantioselective heterogeneous catalysis .2. Examination of the formation of the individual (R) and (S) lactates in the cinchonidine modified platinum hydrogenation of pyruvate [J].
Augustine, RL ;
Tanielyan, SK .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1996, 112 (01) :93-104
[8]   A total asymmetric synthesis of (-)-suaveoline [J].
Bailey, PD ;
Morgan, KM .
CHEMICAL COMMUNICATIONS, 1996, (12) :1479-1480
[9]  
Batista CVF, 1996, PHYTOCHEMISTRY, V41, P969, DOI 10.1016/0031-9422(95)00666-4
[10]  
Belle DD, 1996, TETRAHEDRON, V52, P11361
12345678910