High pressure induced Diels-Alder cycloadditions of butenolides to electron-rich dienes

Rosa M. Ortuño; André Guingant; Jean d'Angelo

doi:10.1016/S0040-4039(00)88496-8

High pressure induced Diels-Alder cycloadditions of butenolides to electron-rich dienes

Rosa M. Ortuño, André Guingant, Jean d'Angelo

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

13 Citations (Scopus)

Abstract

β-Angelica lactone, a model of chiral butenolides, has been efficiently reacted with electron-rich dienes under high pressure conditions, with an excellent diastereofacial, regio- and endo-selectivity, giving the expected adducts in good yields. Some derivatives have been prepared. © 1988.

Original language	English
Pages (from-to)	6989-6992
Journal	Tetrahedron Letters
Volume	29
Issue number	52
DOIs	https://doi.org/10.1016/S0040-4039(00)88496-8
Publication status	Published - 1 Jan 1988

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title = "High pressure induced Diels-Alder cycloadditions of butenolides to electron-rich dienes",

abstract = "β-Angelica lactone, a model of chiral butenolides, has been efficiently reacted with electron-rich dienes under high pressure conditions, with an excellent diastereofacial, regio- and endo-selectivity, giving the expected adducts in good yields. Some derivatives have been prepared. {\textcopyright} 1988.",

author = "Ortu{\~n}o, {Rosa M.} and Andr{\'e} Guingant and Jean d'Angelo",

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T1 - High pressure induced Diels-Alder cycloadditions of butenolides to electron-rich dienes

AU - Ortuño, Rosa M.

AU - Guingant, André

AU - d'Angelo, Jean

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Y1 - 1988/1/1

N2 - β-Angelica lactone, a model of chiral butenolides, has been efficiently reacted with electron-rich dienes under high pressure conditions, with an excellent diastereofacial, regio- and endo-selectivity, giving the expected adducts in good yields. Some derivatives have been prepared. © 1988.

AB - β-Angelica lactone, a model of chiral butenolides, has been efficiently reacted with electron-rich dienes under high pressure conditions, with an excellent diastereofacial, regio- and endo-selectivity, giving the expected adducts in good yields. Some derivatives have been prepared. © 1988.

U2 - 10.1016/S0040-4039(00)88496-8

DO - 10.1016/S0040-4039(00)88496-8

M3 - Article

VL - 29

SP - 6989

EP - 6992

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 52

ER -

High pressure induced Diels-Alder cycloadditions of butenolides to electron-rich dienes

Abstract

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