Publication:
Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Issued Date

2001-07-30

Resource Type

Article

ISSN

09574166

DOI

10.1016/S0957-4166(01)00345-7

Other identifier(s)

2-s2.0-0035973760

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Asymmetry. Vol.12, No.13 (2001), 1913-1922

Suggested Citation

Palangpon Kongsaeree, Puttinan Meepowpan, Yodhathai Thebtaranonth Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions. Tetrahedron Asymmetry. Vol.12, No.13 (2001), 1913-1922. doi:10.1016/S0957-4166(01)00345-7 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/26492

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Title

Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Author(s)

Palangpon Kongsaeree
 Puttinan Meepowpan
 Yodhathai Thebtaranonth

Other Contributor(s)

Mahidol University
 Thailand National Center for Genetic Engineering and Biotechnology

Abstract

Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts. © 2001 Elsevier Science Ltd. All rights reserved.

Keyword(s)

Chemical Engineering
 Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/26492

Collections

Scopus 2001-2005