Synthesis and evaluation of C-seco paclitaxel analogs

被引:39
作者
Appendino, G
Danieli, B
Jakupovic, J
Belloro, E
Scambia, G
Bombardelli, E
机构
[1] CNR, DIPARTIMENTO CHIM ORGAN & IND, I-20133 MILAN, ITALY
[2] CNR, CTR STUDIO SOSTANZE ORGAN NAT, I-20133 MILAN, ITALY
[3] TECH UNIV BERLIN, INST ORGAN CHEM, D-10623 BERLIN, GERMANY
[4] UNIV CATTOLICA SACRO CUORE, IST CLIN OSTETR & GINECOL, I-00168 ROME, ITALY
[5] INDENA SPA, I-20141 MILAN, ITALY
关键词
D O I
10.1016/S0040-4039(97)00877-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Starting from 7,9-diTes-10-dehydro C-secobaccatin III (4a), C-seco analogues of paclitaxel retaining biological activity were synthesised. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:4273 / 4276
页数:4
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