133377-94-3Relevant academic research and scientific papers
Highly stereoselective radical addition to 3-Hydroxy-1-(methylthio)-1-(p-tolylsulfonyl)-1-alkanes and its application to the preparation of optically active compounds
Kayano, Akio,Akazome, Motohiro,Fujita, Makoto,Ogura, Katsuyuki
, p. 12101 - 12114 (2007/10/03)
Efficient 1,2-asymmetric induction was realized in the addition of a 1-hydroxyalkyl radical (R2C-OH to 3-hydroxy-1-methylthio)-1-(p-tolylsulfonyl)-1-alkenes and their acetates (1): Irradiation of 1 and benzophenone in an alcohol (R2CHOH) gave a
Enantiospecific and diastereoselective synthesis of C11-C17 fragment of tylonolide from "asymmetrized tris (hydroxymethyl)methane"
Guanti, Giuseppe,Banfi, Luca,Ghiron, Chiara,Narisano, Enrica
, p. 267 - 270 (2007/10/02)
The fragment C11-C17 of tylonolide 2 was straightforwardly and stereoselectively synthesized starting from monoacetate 5, which is a synthetic equivalent of "asymmetrized tris (hydroxymethyl)methane" 3.
