Synthetic methods and reactions 104. Silylations with in situ generated trimethylsilyl triflate reagent systems
…, BGB Gupta, GF Salem, SC Narang
Index: Olah, George A.; Narang, Subhash C.; Salem, George F.; Gupta, B. G. Balaram Synthesis, 1981 , # 2 p. 142 - 143
Full Text: HTML
Citation Number: 86
Abstract
The trimethylsilyl group is a widely used protecting group for carboxylic acids, alcohols, mercaptans, carbonyl, and nitro compunds.2 Recently, ita usefulness was also demonstrated as an activating group, for example, for carboxylic acids, in the transesterification of carboxylic esters under essentially neutral condition^.^ Although there are numerous reports on different silylation methods, most of them involve basic condition^.^.^ Recently, sily- lations under ...
Related Articles:
Zinc promoted mild and efficient method for the esterification of acid chlorides with alcohols
[Yadav; Reddy, Gondi Sudershan; Srinivas, Dale; Himabindu, Konuru Synthetic Communications, 1998 , vol. 28, # 13 p. 2337 - 2342]
[Aston; Greenburg Journal of the American Chemical Society, 1940 , vol. 62, p. 2593]
[Aimo,G. et al. Synthesis, 1979 , p. 223 - 227]
4-Dialkylaminopyridines as Acylation Catalysts; III1. Acylation of Sterically Hindered Alcohols
[Hoefle,G.; Steglich,W. Synthesis, 1972 , p. 619 - 621]
[Jenkins, Jerry A.; Mendenhall, G. David Journal of Organic Chemistry, 1981 , vol. 46, # 20 p. 3997 - 4000]