Synthesis of azetidine-type taxanes

被引:28
作者
Fenoglio, I [1 ]
Nano, GM [1 ]
VanderVelde, DG [1 ]
Appendino, G [1 ]
机构
[1] UNIV KANSAS,DEPT MED CHEM,LAWRENCE,KS 66045
关键词
D O I
10.1016/0040-4039(96)00495-9
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Starting from the alkaloid 2'-deacetoxyaustrospicatine (2) azetidine isosteres of the oxetane-type taxane I 1-deoxy-2-debenzoyloxy-4-deacetylbaccatin VI were synthesised. Copyright (C) 1996 Elsevier Science Ltd
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页码:3203 / 3206
页数:4
相关论文
共 19 条
[1]   THE PHYTOCHEMISTRY OF THE YEW TREE [J].
APPENDINO, G .
NATURAL PRODUCT REPORTS, 1995, 12 (04) :349-360
[2]  
APPENDINO G, 1996, IN PRESS ALKALOIDS C
[3]  
APPENDINO G, 1996, TETRAHEDRON LETT, P727
[4]   SYNTHETIC STUDIES TOWARDS TAXOL ANALOGS - CHEMOSELECTIVE CLEAVAGE OF C-5 CINNAMOYL GROUP IN TAXANE GROUP OF DITERPENOIDS WITH HYDROXYLAMINE [J].
BATHINI, Y ;
MICETICH, RG ;
DANESHTALAB, M .
SYNTHETIC COMMUNICATIONS, 1994, 24 (11) :1513-1517
[5]   THE CHEMISTRY OF TAXANES - REACTION OF TAXOL AND BACCATIN DERIVATIVES WITH LEWIS-ACIDS IN APROTIC AND PROTIC MEDIA [J].
CHEN, SH ;
HUANG, S ;
WEI, JM ;
FARINA, V .
TETRAHEDRON, 1993, 49 (14) :2805-2828
[6]  
CHEN SH, 1995, CHEM PHARM TAXOL R I, V5, P165
[7]   THE TAXOL SUPPLY CRISIS - NEW NCI POLICIES FOR HANDLING THE LARGE-SCALE PRODUCTION OF NOVEL NATURAL PRODUCT ANTICANCER AND ANTI-HIV AGENTS [J].
CRAGG, GM ;
SCHEPARTZ, SA ;
SUFFNESS, M ;
GREVER, MR .
JOURNAL OF NATURAL PRODUCTS, 1993, 56 (10) :1657-1668
[8]   ROOM TEMPERATURE WOLFF-KISHNER REDUCTION AND COPE ELIMINATION REACTIONS [J].
CRAM, DJ ;
SAHYUN, MRV ;
KNOX, GR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1962, 84 (09) :1734-&
[9]  
ETTOUATI L, 1988, B SOC CHIM FR, P749
[10]   1ST HEMISYNTHESIS OF A TAXANE COMPOUND WITH AN OXETANE GROUP IN POSITION 4 (20), 5 [J].
ETTOUATI, L ;
AHOND, A ;
POUPAT, C ;
POTIER, P .
TETRAHEDRON, 1991, 47 (47) :9823-9838