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

doi:10.1002/recl.19951140803

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

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-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 language	English
Pages (from-to)	357-360
Journal	Recueil des Travaux Chimiques des Pays‐Bas
Volume	114
Issue number	8
DOIs	https://doi.org/10.1002/recl.19951140803
Publication status	Published - 1 Jan 1995

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

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 {\textcopyright} 1995 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim",

author = "{de March}, P. and M. Figueredo and J. Font and M. Monsalvatje",

year = "1995",

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doi = "10.1002/recl.19951140803",

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T1 - Reactions of cyclic nitrones with (E)‐γ‐hydroxy‐ and (E)‐γ‐alkoxy‐α,β‐unsaturated esters

AU - de March, P.

AU - Figueredo, M.

AU - Font, J.

AU - Monsalvatje, M.

PY - 1995/1/1

Y1 - 1995/1/1

N2 - 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

AB - 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

U2 - 10.1002/recl.19951140803

DO - 10.1002/recl.19951140803

M3 - Article

VL - 114

SP - 357

EP - 360

IS - 8

ER -

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

Abstract

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