807626-27-3Relevant academic research and scientific papers
Chiral 3-hydroxypyrrolidin-2-ones. Part 2: Stereodivergent synthesis of conformationally restricted analogues of β-homoserine
Galeazzi, Roberta,Martelli, Gianluca,Natali, Desire,Orena, Mario,Rinaldi, Samuele
, p. 1779 - 1787 (2007/10/03)
Starting from the homochiral 3-t-butyldimethylsilyloxypyrrolidin-2-one 2, a stereodivergent synthetic route was developed leading to both 3,4-trans- and 3,4-cis-3-amino-4-hydroxymethyl pyrrolidin-2-ones, 19 and 28, that are conformationally restricted ana
Chiral 3-hydroxypyrrolidin-2-ones from a Baylis-Hillman adduct: Convergent, stereoselective synthesis of a glycosidase inhibitor
Galeazzi, Roberta,Martelli, Gianluca,Mobbili, Giovanna,Orena, Mario,Rinaldi, Samuele
, p. 3249 - 3256 (2007/10/03)
The O-silyl derivative 4b, prepared starting from the Baylis-Hillman adduct 4a, underwent cyclization on treatment with (S)-phenylethylamine, to give to an equimolar mixture of the 4,5-cis-disubstituted pyrrolidin-2-ones 9 and 10, exclusively, which after
