| Literature DB >> 27603590 |
Kevin X Rodriguez1, Justin D Vail1, Brandon L Ashfeld1.
Abstract
A phosphorus(III)-mediated formal [4+1]-cycloaddition of 1,2-dicarbonyls and o-quinone methides to provide 2,3-dihydrobenzofurans is described. By exploiting the carbene-like nature of dioxyphospholenes, dihydrobenzofurans bearing a quaternary center at C2 are obtained in 30-92% yield with diastereoselectivities up to ≥20:1. This study highlights the subtle steric interactions involved in the [4+1]-cycloannulation and the impact they have on yield and stereoselectivity in dihydrobenzofuran formation.Entities:
Year: 2016 PMID: 27603590 DOI: 10.1021/acs.orglett.6b02122
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005