Publication:
The application of the Baker-Venkataraman rearrangement to the synthesis of benz[b]indeno[2,1-e]pyran-10,11-dione

Issued Date

2002-01-01

Resource Type

Article

ISSN

00404039

DOI

10.1016/S0040-4039(02)00818-3

Other identifier(s)

2-s2.0-0037124408

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Letters. Vol.43, No.25 (2002), 4515-4517

Suggested Citation

Nopporn Thasana, Somsak Ruchirawat The application of the Baker-Venkataraman rearrangement to the synthesis of benz[b]indeno[2,1-e]pyran-10,11-dione. Tetrahedron Letters. Vol.43, No.25 (2002), 4515-4517. doi:10.1016/S0040-4039(02)00818-3 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/20107

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Title

The application of the Baker-Venkataraman rearrangement to the synthesis of benz[b]indeno[2,1-e]pyran-10,11-dione

Author(s)

Nopporn Thasana
 Somsak Ruchirawat

Other Contributor(s)

Chulabhorn Research Institute
 Mahidol University
 The Institute of Science and Technology for Research and Development, Mahidol University

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.

Keyword(s)

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

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URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/20107

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Scopus 2001-2005