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Updated: Jul 11, 2026

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

Reacciones acil-pictet-spengler catalíticas muy enantioselectivas y altamente enantioselectivas

Mark S Taylor1, Eric N Jacobsen

  • 1Harvard University, Department of Chemistry and Chemical Biology, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.

Journal of the American Chemical Society
|August 26, 2004
PubMed
Resumen

Un nuevo catalizador quiral de tiurea permite una alta enantioselectividad en la reacción de Pictet-Spengler a través de la ciclización de iones de N-acilíminio. Este avance marca la primera catálisis asimétrica exitosa para esta importante reacción.

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