New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process

Philippe Diaz; Fabrice Gendre; Lucien Stella; Bruno Charpentier

doi:10.1016/S0040-4020(98)00169-0

New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process

Philippe Diaz, Fabrice Gendre, Lucien Stella, Bruno Charpentier

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69 Scopus citations

Abstract

A new series of conformationally restricted retinoids (3-aryl-3-methyl- 2,3-dihydrobenzofurans) have been prepared through a palladium-catalyzed tandem cyclisation-hydride capture. The use of enantiopure BINAP-Pd catalyst allowed asymmetric synthesis of bioactive molecules.

Original language	English
Pages (from-to)	4579-4590
Number of pages	12
Journal	Tetrahedron
Volume	54
Issue number	18
DOIs	https://doi.org/10.1016/S0040-4020(98)00169-0
State	Published - Apr 30 1998

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title = "New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process",

abstract = "A new series of conformationally restricted retinoids (3-aryl-3-methyl- 2,3-dihydrobenzofurans) have been prepared through a palladium-catalyzed tandem cyclisation-hydride capture. The use of enantiopure BINAP-Pd catalyst allowed asymmetric synthesis of bioactive molecules.",

author = "Philippe Diaz and Fabrice Gendre and Lucien Stella and Bruno Charpentier",

year = "1998",

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T1 - New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process

AU - Diaz, Philippe

AU - Gendre, Fabrice

AU - Stella, Lucien

AU - Charpentier, Bruno

PY - 1998/4/30

Y1 - 1998/4/30

N2 - A new series of conformationally restricted retinoids (3-aryl-3-methyl- 2,3-dihydrobenzofurans) have been prepared through a palladium-catalyzed tandem cyclisation-hydride capture. The use of enantiopure BINAP-Pd catalyst allowed asymmetric synthesis of bioactive molecules.

AB - A new series of conformationally restricted retinoids (3-aryl-3-methyl- 2,3-dihydrobenzofurans) have been prepared through a palladium-catalyzed tandem cyclisation-hydride capture. The use of enantiopure BINAP-Pd catalyst allowed asymmetric synthesis of bioactive molecules.

UR - https://www.scopus.com/pages/publications/0032580391

U2 - 10.1016/S0040-4020(98)00169-0

DO - 10.1016/S0040-4020(98)00169-0

M3 - Article

AN - SCOPUS:0032580391

SN - 0040-4020

VL - 54

SP - 4579

EP - 4590

JO - Tetrahedron

JF - Tetrahedron

IS - 18

ER -

New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process

Abstract

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