| Literature DB >> 26818590 |
William Doherty1, Paul Evans1.
Abstract
An operationally simple protocol for the synthesis of γ-hydroxy vinyl sulfones has been developed using a proline-based aldehyde aminooxylation, followed by a vinyl sulfone forming Horner-Wadsworth-Emmons olefination. The adducts, formed in high enantiopurity, were subsequently converted to γ-azido vinyl sulfones, and azide-alkyne click chemistry enabled the synthesis of vinyl sulfone-based triazoles as potential nonpeptidic cysteine protease inhibitors.Entities:
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Year: 2016 PMID: 26818590 DOI: 10.1021/acs.joc.5b02556
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354