150176-19-5Relevant academic research and scientific papers
Carbon based nucleophilic ring opening of activated monocyclic β-lactams; synthesis and stereochemical assignment of the ACE inhibitor WF-10129
Baldwin, Jack E.,Adlington, Robert M.,Russell, Andrew T.,Smith, Marie L.
, p. 4733 - 4762 (1995)
The preparation of γ-keto α-amino acids via carbon based nucleophilic ring opening of activated monocyclic β-lactams was examined and applied to the synthesis and stereochemical assignment of the dipeptide angiotensin convering enzyme (ACE) inhibitor, WF-
Preparation of lactones with several ring sizes via the same intermediate
Robin,Huet
, p. 2945 - 2948 (2007/10/02)
Several lactones were prepared from (S)-1-(phenylsufonyl)-3-butanol 2 by cyclization of alkylation products of its silyl derivative 3 with electrophilic reagents bearing a functional group.
