Publication:
Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Issued Date

1999-01-01

Resource Type

Article

ISSN

09365214

DOI

10.1055/s-1999-2825

Other identifier(s)

2-s2.0-0032806759

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Synlett. No.8 (1999), 1307-1309

Suggested Citation

Roderick W. Bates, Palangpon Kongsaeree Diastereoselectivity in Michael additions to a pyrrolidinyl enone. Synlett. No.8 (1999), 1307-1309. doi:10.1055/s-1999-2825 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/25387

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Title

Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Author(s)

Roderick W. Bates
 Palangpon Kongsaeree

Other Contributor(s)

Chulalongkorn University
 Chulabhorn Research Institute
 Mahidol University

Abstract

Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.

Keyword(s)

Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/123456789/25387

Collections

Scopus 1991-2000