Reactions of cyclic nitrones with (E)‐γ‐hydroxy‐ and (E)‐γ‐alkoxy‐α,β‐unsaturated esters

P. de March, M. Figueredo, J. Font, M. Monsalvatje

Research output: Contribution to journalArticleResearchpeer-review

14 Citations (Scopus)

Abstract

The 1,3‐dipolar cycloadditions of 2,3,4,5‐tetrahydropyridine 1‐oxide (1) and 3,4‐dihydro‐2H‐pyrrole 1‐oxide (2) to methyl (E)‐6‐(benzyloxy)‐4‐hydroxy‐2‐hexenoate (3) and methyl (S)‐(E)‐3‐(2,2‐dimethyl‐1,3‐dioxolan‐4‐yl)propenoate (4) yield predominantly the adducts derived from endo transition states with antifacial approaches. Copyright © 1995 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
Original languageEnglish
Pages (from-to)357-360
JournalRecueil des Travaux Chimiques des Pays‐Bas
Volume114
Issue number8
DOIs
Publication statusPublished - 1 Jan 1995

Fingerprint Dive into the research topics of 'Reactions of cyclic nitrones with (E)‐γ‐hydroxy‐ and (E)‐γ‐alkoxy‐α,β‐unsaturated esters'. Together they form a unique fingerprint.

Cite this