Antarafacial mediation of oxygen delivery by a phenylsulfinyl group in the epoxidation of proximal double bonds: Intramolecular trapping of an early Pummerer intermediate with stereoelectronic control Journal Article


Authors: Zhang, Y.; Lee, J. H.; Danishefsky, S. J.
Article Title: Antarafacial mediation of oxygen delivery by a phenylsulfinyl group in the epoxidation of proximal double bonds: Intramolecular trapping of an early Pummerer intermediate with stereoelectronic control
Abstract: Stereospecific intramolecular antarafacial epoxidation of a double bond via an early Pummerer reaction intermediate has been demonstrated. The intermediate is presumably generated via trifluoroacetylation of a sulfoxide precursor. Ionization of trifluoroacetate would formally generate a dipositive "sulfenium" equivalent. This species attacks an otherwise unactivated, proximal olefinic linkage in an antiperiplanar fashion, with trifluoroacetate serving as the nucleophile. Proposed mechanistic intermediates were characterized structurally (in several cases by crystallographic means) and shown to serve as precursors en route to the final antarafacial epoxides. The sense of the cyclization seems to be driven by principles inherent in Markovnikov's rule. © 2010 American Chemical Society.
Journal Title: Journal of the American Chemical Society
Volume: 133
Issue: 4
ISSN: 0002-7863
Publisher: American Chemical Society  
Date Published: 2011-02-02
Start Page: 752
End Page: 755
Language: English
DOI: 10.1021/ja1107707
PROVIDER: scopus
PMCID: PMC3030660
PUBMED: 21182300
DOI/URL:
Notes: --- - "Export Date: 4 March 2011" - "CODEN: JACSA" - "Source: Scopus"
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