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Transition-Metal Catalysis of the Michael Reaction of 1,3-Dicarbonyl Compounds and Acceptor-Activated Alkenes

✍ Scribed by Jens Christoffers


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
310 KB
Volume
1998
Category
Article
ISSN
1434-193X

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From the standpoint of atom efficiency, [1] nucleophilic additions to alkenes or alcohols instead of alkyl halides are attractive salt-free methods (Scheme 1). Simple alkenes are readily accessible and abundant carbon-atom sources, but intermolecular additions of 1,3-dicarbonyl compounds to simple a