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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/20107
Title: The application of the Baker-Venkataraman rearrangement to the synthesis of benz[b]indeno[2,1-e]pyran-10,11-dione
Authors: Nopporn Thasana
Somsak Ruchirawat
Chulabhorn Research Institute
Mahidol University
The Institute of Science and Technology for Research and Development, Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Jan-2002
Citation: Tetrahedron Letters. Vol.43, No.25 (2002), 4515-4517
Abstract: A tetracyclic benzocyclopentabenzopyran-4-one was synthesized via a domino reaction involving an initial aroyl transfer as in the Baker-Venkataraman rearrangement. The derived 1,3 diketone underwent the intramolecular acylation followed by cyclization to give the product. © 2002 Elsevier Science Ltd. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037124408&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/20107
ISSN: 00404039
Appears in Collections:Scopus 2001-2005

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