A convenient procedure for the direct conversion of terminal alkenes into carboxylic acids
摘要:
Alkylboronic acids, readily synthesized from a variety of representative terminal alkenes via hydroboration with dibromoborane-methyl sulfide, undergo a facile oxidation with chromium trioxide in 90% aqueous acetic acid to provide carboxylic acids in 80-97% isolated yields, without rearrangement or loss of carbon.
Fisher, Gary B.; Juarez-Brambila, Jesus J.; Gorakki, Christian T., Journal of the American Chemical Society, 1993, vol. 115, # 2, p. 440 - 444
作者:Fisher, Gary B.、Juarez-Brambila, Jesus J.、Gorakki, Christian T.、Wipke, W. Todd、Singaram, Bakthan
DOI:——
日期:——
A convenient procedure for the direct conversion of terminal alkenes into carboxylic acids
作者:Uday S. Racherla、Vijay V. Khanna、Herbert C. Brown
DOI:10.1016/s0040-4039(00)91853-7
日期:1992.2
Alkylboronic acids, readily synthesized from a variety of representative terminal alkenes via hydroboration with dibromoborane-methyl sulfide, undergo a facile oxidation with chromium trioxide in 90% aqueous acetic acid to provide carboxylic acids in 80-97% isolated yields, without rearrangement or loss of carbon.
207. Peroxides of elements other than carbon. Part IX. The course of the autoxidation of tris-2-methylpentylboron and tri-n-butylboron