A novel utilization of trifluoromethanide as a base: a convenient synthesis of trimethylsilylacetylene
M Yoshimatsu, M Kuribayashi
Index: Yoshimatsu, Mitsuhiro; Kuribayashi, Masako Journal of the Chemical Society. Perkin Transactions 1, 2001 , # 11 p. 1256 - 1257
Full Text: HTML
Citation Number: 0
Abstract
Trifluoromethyltrimethylsilane (Ruppert's reagent, CF 3 SiMe 3 ) has recently attracted attention as a source of the trifluoromethyl functional group, and has been widely used for the conversions of aldehydes and ketones to trifluoromethyl alcohols, 1 of esters to trifluoromethyl ketones 2 and of azirines to trifluoromethylaziridines. 3 In particular, the reactions of acylsilanes with CF 3 SiMe 3 have produced the versatile intermediate, difluoroenoxysilane, which is readily ...
Related Articles:
[Sugiyama, Jiro; Tomita, Ikuyoshi European Journal of Organic Chemistry, 2007 , # 28 p. 4651 - 4653]
[Semba, Kazuhiko; Fujihara, Tetsuaki; Xu, Tinghua; Terao, Jun; Tsuji, Yasushi Advanced Synthesis and Catalysis, 2012 , vol. 354, # 8 p. 1542 - 1550]
[Gung, Benjamin W.; Kumi, Godwin Journal of Organic Chemistry, 2004 , vol. 69, # 10 p. 3488 - 3492]
[Graham, Erin R.; Tykwinski, Rik R. Journal of Organic Chemistry, 2011 , vol. 76, # 16 p. 6574 - 6583]
[Negishi, Ei-ichi; Okukado, Nobuhisa; Lovich, Stephen F.; Luo, Fen-Tair Journal of Organic Chemistry, 1984 , vol. 49, # 14 p. 2629 - 2632]