The total synthesis of (±)-11-O-debenzoyltashironin Journal Article


Authors: Cook, S. P.; Polara, A.; Danishefsky, S. J.
Article Title: The total synthesis of (±)-11-O-debenzoyltashironin
Abstract: The total synthesis of the putative non-peptidyl neurotrophic factor 11-O-debenzoyltashironin has been accomplished. The key transformation involves a biomimetic oxidative dearomatization/transannular Diels-Alder sequence that closes the tetracyclic carbon skeleton present in the natural product. Copyright © 2006 American Chemical Society.
Keywords: unclassified drug; drug activity; drug synthesis; chemistry; chemical structure; molecular structure; cyclization; natural product; oxidation; diels alder reaction; oxidation reduction reaction; oxidation-reduction; synthesis; stereoisomerism; carbon; bridged compounds; annulation reaction; aromatization; 11 o debenzoyltashironin; nerve cell growth; illicium; 11-o-debenzoyltashironin; bridged compound
Journal Title: Journal of the American Chemical Society
Volume: 128
Issue: 51
ISSN: 0002-7863
Publisher: American Chemical Society  
Date Published: 2006-12-27
Start Page: 16440
End Page: 16441
Language: English
DOI: 10.1021/ja0670254
PUBMED: 17177359
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 30" - "Export Date: 4 June 2012" - "CODEN: JACSA" - "Source: Scopus"
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