A concise route to benzofused macrolactones via ynolides: Cycloproparadicicol Journal Article


Authors: Yang, Z. Q.; Danishefsky, S. J.
Article Title: A concise route to benzofused macrolactones via ynolides: Cycloproparadicicol
Abstract: A new facile synthesis has been developed for nanomolar Hsp90 inhibitor, cycloproparadicicol (2). Our approach relied on cobalt-complexation promoted RCM, in combination with tandem Diels-Alder/retro-Diels-Alder reactions to assemble the resorcycinylic macrolactone. Copyright © 2003 American Chemical Society.
Keywords: unclassified drug; drug activity; antineoplastic agent; drug synthesis; cyclopropanes; cyclization; macrolide; technique; chemical reaction; ring closing metathesis; cycloproparadicicol; lactone derivative; cycloaddition; lactones; macrolides; resorcinols; article
Journal Title: Journal of the American Chemical Society
Volume: 125
Issue: 32
ISSN: 0002-7863
Publisher: American Chemical Society  
Date Published: 2003-08-13
Start Page: 9602
End Page: 9603
Language: English
DOI: 10.1021/ja036192q
PUBMED: 12904022
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
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  1. Zhi-Qiang Yang
    5 Yang