Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59353
Title: Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
Authors: Rattana Jongkol
Ruangrat Choommongkol
Bongkoch Tarnchompoo
Piyarat Nimmanpipug
Puttinan Meepowpan
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 8-Aug-2009
Abstract: The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/59353
ISSN: 00404020
Appears in Collections:CMUL: Journal Articles

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