Tandem Palladium‐Catalyzed Cyclocarbonylation of Isolimonene: A Mechanistic Investigation and Theoretical Calculations on the Fully Diastereoselective Step-Reference-Cited by-同舟云学术

Tandem Palladium‐Catalyzed Cyclocarbonylation of Isolimonene: A Mechanistic Investigation and Theoretical Calculations on the Fully Diastereoselective Step

Published:2004-02 Issue:4 Volume:2004 Page:791-797
ISSN:1434-1948
Container-title:European Journal of Inorganic Chemistry
language:en
Short-container-title:Eur. J. Inorg. Chem.

Author:

Lenoble Géraldine¹,Lacaze‐Dufaure Corinne²,Urrutigoïty Martine¹,Mijoule Claude²,Kalck Philippe¹

Affiliation:

1. Laboratoire de Catalyse, Chimie Fine et Polymères, Ecole Nationale Supérieure des Ingénieurs en Arts Chimiques et Technologiques 118 route de Narbonne, 31077 Toulouse Cedex 4, France, Fax: (internat.) + 33‐5‐62885600

2. CIRIMAT, Laboratoire des Interfaces et Matériaux, Ecole Nationale Supérieure des Ingénieurs en Arts Chimiques et Technologiques 118 route de Narbonne, 31077 Toulouse Cedex 4, France

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.200300540

Reference40 articles.

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5. Carbon monoxide as a building block in organic synthesis. Part V. Involvement of palladium-hydride species in carbonylation reactions of monoterpenes. X-ray crystal structure of [Ph3PCH2CHCHPh]4[PdCl6][SnCl6]

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