199850-05-0Relevant articles and documents
Modified Yamaguchi reagent: Convenient and efficient esterification
Okuno, Yoshinori,Isomura, Shigeki,Nishibayashi, Akihiro,Hosoi, Aiko,Fukuyama, Kei,Ohba, Masashi,Takeda, Kazuyoshi
supporting information, p. 2854 - 2860 (2014/10/15)
A convenient and efficient esterification method that used a modified Yamaguchi reagent (2,4,6-trichlorobenzoyl chloride-4-dimethylaminopyridine) and avoided use not only of intractable acid chloride but also of acid anhydrides was proposed. The reaction mechanism was described by Fourier transform infrared spectroscopy and supported by a density functional theory calculation.
Kinetic resolution of secondary alcohols by NHC-catalyzed oxidative esterification
Desarkar, Suman,Biswas, Anup,Song, Chie Hoon,Studer, Armido
experimental part, p. 1974 - 1983 (2011/07/07)
Kinetic resolution of racemic secondary alcohols by oxidative esterification using carbene catalysis is described. Good to moderate selectivity has been achieved. N-Heterocyclic carbenes (NHCs) were systematically varied and several aldehydes were included in this study as acyl donors. As an oxidant, a readily available bisquinone-type system was used. Georg Thieme Verlag Stuttgart - New York.