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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:
CreatorsEmailPitt UsernameORCID
Mandel, AL
Bellosta, V
Curran, DPcurran@pitt.eduCURRAN
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.pitt.edu/id/eprint/17349

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