A new metal mediated stereocontrolled synthesis of allylic fluorides

被引:21
作者
Madiot, V [1 ]
Grée, D [1 ]
Grée, R [1 ]
机构
[1] Ecole Natl Super Chim Rennes, CNRS, Lab Synth & Activat Biomol, F-35700 Rennes, France
关键词
D O I
10.1016/S0040-4039(99)01330-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Propargylic fluorides are converted in a short sequence involving hydrostannylation, iodination and Pd catalysis into new stereodefined polyunsaturated systems with a fluorine atom in the allylic position. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:6403 / 6406
页数:4
相关论文
共 23 条
[21]   CONVENIENT SYNTHESIS OF ACETYLENES - CATALYTIC SUBSTITUTIONS OF ACETYLENIC HYDROGEN WITH BROMOALKENES, IODOARENES, AND BROMOPYRIDINES [J].
SONOGASHIRA, K ;
TOHDA, Y ;
HAGIHARA, N .
TETRAHEDRON LETTERS, 1975, (50) :4467-4470
[22]   ADVANCES IN THE PREPARATION OF BIOLOGICALLY-ACTIVE ORGANOFLUORINE COMPOUNDS [J].
WELCH, JT .
TETRAHEDRON, 1987, 43 (14) :3123-3197
[23]  
ENANTIOCONTROLLED SY