Publication:
Stereospecific triple Michael addition

Issued Date

1986-01-01

Resource Type

Article

ISSN

00404039

DOI

10.1016/S0040-4039(00)84512-8

Other identifier(s)

2-s2.0-0344389224

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Letters. Vol.27, No.20 (1986), 2295-2298

Suggested Citation

Chatchai Thanupran, Chachanat Thebtaranonth, Yodhathai Thebtaranonth Stereospecific triple Michael addition. Tetrahedron Letters. Vol.27, No.20 (1986), 2295-2298. doi:10.1016/S0040-4039(00)84512-8 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/9674

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Title

Stereospecific triple Michael addition

Author(s)

Chatchai Thanupran
 Chachanat Thebtaranonth
 Yodhathai Thebtaranonth

Other Contributor(s)

Mahidol University

Abstract

The consecutive Michael addition of a nucleophile to an α -methylene cyclopentenone, thence to methyl acrylate, occurs readily and stereospecifically, yielding bicyclo-[2,2,1]-heptanone. The reaction represents the first example of a three-component triple conjugate addition process. © 1986.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Chemistry
 Pharmacology, Toxicology and Pharmaceutics

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/9674

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Scopus 1969-1990