Related Experiment Video
Updated: May 4, 2026
Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Autotandem catalysis with ruthenium: remote hydroesterification of allylic amides
Nicolas Armanino1, Marc Lafrance, Erick M Carreira
1Laboratorium für Organische Chemie, ETH Zürich , CH-8093 Zürich, Switzerland.
Abstract:
A one-pot tandem sequence involving olefin isomerization and hydroesterification has been developed that enables the incorporation of a C1-unit at the remote terminal position of allylic amides. Key observations suggest that generation of an active ruthenium hydride, formed by addition of acetic acid, allows both processes to take place under mild conditions in an autotandem catalytic, cascading fashion, which is characterized by the use of a single catalytic entity capable of promoting multiple distinct steps without operator intervention.
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