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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|
Chulabhorn Research Institute
The Institute of Science and Technology for Research and Development, Mahidol University
|Keywords:||Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics|
|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.|
|Appears in Collections:||Scopus 2001-2005|
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