| Literature DB >> 16719448 |
Brian G Pujanauski1, B A Bhanu Prasad, Richmond Sarpong.
Abstract
A Pt-catalyzed pentannulation of propargylic esters containing an epoxide moiety has been developed. The present transformation achieves the formation of cyclopentenone products as single diastereomers in good yields. The observed products likely form from pyran intermediates that undergo an oxa-6pi electrocyclic ring opening to a functionalized dienone, followed by ring closure with an accompanying acyl shift.Entities:
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Year: 2006 PMID: 16719448 DOI: 10.1021/ja061549m
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419