Highly Stereoselective Epoxidation of α-Methyl-γ-hydroxy-α,β-unsaturated Esters: Rationalization and Synthetic Applications
Author:
Affiliation:
1. Departament de Química Inorgànica i Orgànica Universitat Jaume I, 12080 Castelló, Spain %fgonzale@qio.uji.es
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0709955
Reference21 articles.
1. Regioselective openings of 2,3-epoxy acids with organocuprates
2. Ring-opening of β-F-alkyl α,β-epoxyesters with NaBH4 in alcoholic media
3. Stereoselective Preparation of Syn α-Hydroxy-β-amino Ester Units via Regioselective Opening of α,β-Epoxy Esters: Enantioselective Synthesis of Taxol C-13 Side Chain and Cyclohexylnorstatine
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