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Palladium-Catalyzed Diastereoselective Synthesis of Isoindolinones

Palladium-Catalyzed Diastereoselective Synthesis of Isoindolinones Abstract: 2-Bromobenzaldehyde reacts diastereoselectively with chiral alkanolamines under carbon monoxide in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride to afford the corresponding tricyclic isoindolinones in moderate to good yields. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Synthetic Communications Taylor & Francis

Palladium-Catalyzed Diastereoselective Synthesis of Isoindolinones

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References (13)

Publisher
Taylor & Francis
Copyright
Copyright Taylor & Francis Group, LLC
ISSN
1532-2432
eISSN
0039-7911
DOI
10.1080/00397919708005462
Publisher site
See Article on Publisher Site

Abstract

Abstract: 2-Bromobenzaldehyde reacts diastereoselectively with chiral alkanolamines under carbon monoxide in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride to afford the corresponding tricyclic isoindolinones in moderate to good yields.

Journal

Synthetic CommunicationsTaylor & Francis

Published: Dec 1, 1997

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