A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A

Mandel, AL and Bellosta, V and Curran, DP and Cossy, J (2009) A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A. Organic Letters, 11 (15). 3282 - 3285. ISSN 1523-7060

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Abstract

A versatile synthetic approach to the tulearin class of macrolactones has been developed and deployed to make a stereoisomer of tulearin A. The knowledge gained about structure and synthesis will expedite the assignment of the stereostructure of this new anticancer agent. © 2009 American Chemical Society.

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Details

Item Type:	Article
Status:	Published
Creators/Authors:	Creators Email Pitt Username ORCID Mandel, AL Bellosta, V Curran, DP curran@pitt.edu CURRAN Cossy, J
Date:	6 August 2009
Date Type:	Publication
Journal or Publication Title:	Organic Letters
Volume:	11
Number:	15
Page Range:	3282 - 3285
DOI or Unique Handle:	10.1021/ol900936t
Schools and Programs:	Dietrich School of Arts and Sciences > Chemistry
Refereed:	Yes
ISSN:	1523-7060
MeSH Headings:	Anticarcinogenic Agents--chemical synthesis; Anticarcinogenic Agents--chemistry; Macrolides--chemical synthesis; Macrolides--chemistry; Stereoisomerism
Other ID:	NLM NIHMS128190, NLM PMC2736336
PubMed Central ID:	PMC2736336
PubMed ID:	19555117
Date Deposited:	21 Feb 2013 22:54
Last Modified:	02 Feb 2019 15:58
URI:	http://d-scholarship-dev.library.pitt.edu/id/eprint/17349

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