June 24, 2004Organic Letters

Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones

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Authors

SCSylvain CoutyInstitute of Cancer Research BLBenoît LiégaultÉcole Nationale Supérieure de Chimie de Montpellier CMChristophe MeyerCentre National de la Recherche Scientifique

Abstract

[reaction: see text] Substituted 3-(arylmethylene)isoindolin-1-ones can be efficiently synthesized in a stereoselective manner from various ynamides and boronic acids by palladium-catalyzed Heck-Suzuki-Miyaura domino reactions.

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Couty et al. (2004) studied this question.

synapsesocial.com/papers/6a94c9e89c58c85b0bdbd279 https://doi.org/10.1021/ol049302m

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Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones

Abstract

Discussion

Cite This Study

Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones

Abstract

Discussion

Cite This Study

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