Diels-Alder reactions of protoanemonin with heterosubstituted dienes. Synthesis of polyfunctional oxaspiro[4.5]decanes.

Daniel Alonso; Josep Font; Rosa M. Ortuño; Jean d'Angelo; André Guingant; Claudette Bois

doi:10.1016/S0040-4020(01)86540-6

Diels-Alder reactions of protoanemonin with heterosubstituted dienes. Synthesis of polyfunctional oxaspiro[4.5]decanes.

Daniel Alonso, Josep Font, Rosa M. Ortuño, Jean d'Angelo, André Guingant, Claudette Bois

Department of Chemistry

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

14 Citations (Scopus)

Abstract

Cycloadditions of protoanemonin (1) with different kinds of heterosubstituted dienes have been tried under several reaction conditions; 1 has revealed to be a good dienophile towards electron-rich dienes giving adducts that can be easily transformed into useful synthetic building blocks. © 1991.

Original language	English
Pages (from-to)	5895-5900
Journal	Tetrahedron
Volume	47
Issue number	30
DOIs	https://doi.org/10.1016/S0040-4020(01)86540-6
Publication status	Published - 22 Jul 1991

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title = "Diels-Alder reactions of protoanemonin with heterosubstituted dienes. Synthesis of polyfunctional oxaspiro[4.5]decanes.",

abstract = "Cycloadditions of protoanemonin (1) with different kinds of heterosubstituted dienes have been tried under several reaction conditions; 1 has revealed to be a good dienophile towards electron-rich dienes giving adducts that can be easily transformed into useful synthetic building blocks. {\textcopyright} 1991.",

author = "Daniel Alonso and Josep Font and Ortu{\~n}o, {Rosa M.} and Jean d'Angelo and Andr{\'e} Guingant and Claudette Bois",

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AU - Alonso, Daniel

AU - Font, Josep

AU - Ortuño, Rosa M.

AU - d'Angelo, Jean

AU - Guingant, André

AU - Bois, Claudette

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N2 - Cycloadditions of protoanemonin (1) with different kinds of heterosubstituted dienes have been tried under several reaction conditions; 1 has revealed to be a good dienophile towards electron-rich dienes giving adducts that can be easily transformed into useful synthetic building blocks. © 1991.

AB - Cycloadditions of protoanemonin (1) with different kinds of heterosubstituted dienes have been tried under several reaction conditions; 1 has revealed to be a good dienophile towards electron-rich dienes giving adducts that can be easily transformed into useful synthetic building blocks. © 1991.

U2 - 10.1016/S0040-4020(01)86540-6

DO - 10.1016/S0040-4020(01)86540-6

M3 - Article

VL - 47

SP - 5895

EP - 5900

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

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