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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/18292
Title: γ-Regioselectivity of lithiated 2-buten-4-olide towards aromatic aldehydes: A simple synthesis of γ-arylidenebutenolides
Authors: Manat Pohmakotr
Patoomratana Tuchinda
Pornchai Premkaisorn
Vichai Reutrakul
Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 10-Sep-1998
Citation: Tetrahedron. Vol.54, No.37 (1998), 11297-11304
Abstract: Lithiated 2-buten-4-olide was found to react with aromatic aldehydes regioselectively at γ-position to provide 4-(1-aryl-1-hydroxymethyl)-2- buten-4-olides which could be readily converted into the corresponding (Z)- γ-arylidenebutenolides.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032505193&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/18292
ISSN: 00404020
Appears in Collections:Scopus 1991-2000

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