A direct and useful route to difluoroacylsilanes and difluoroacylstannanes and their potential for the generation of structurally diverse difluoroketones

被引:27
作者
Garayt, MR [1 ]
Percy, JM [1 ]
机构
[1] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1016/S0040-4039(01)01220-5
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Allyl trifluoroethyl ethers 2a-2d were prepared; each underwent efficient dehydrofluorination/metallation and trapping to afford a range of difluoroenol silanes and stannanes which rearranged easily and efficiently to the acyl metals. Fluoride-mediated benzylation and allylation of an acylsilane, and Stille coupling of the vinyl- and acyl-stannane were achieved in moderate to good yield. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:6377 / 6380
页数:4
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