Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis

Wipf, P and Methot, JL (2001) Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis. Organic Letters, 3 (9). 1261 - 1263. ISSN 1523-7060

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Abstract

(equation presented) The indole-bisoxazole fragment of diazonamide A was prepared by a Chan-type rearrangement of a tertiary amide. This approach represents a remarkably direct strategy for polyoxazole synthesis.

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Details

Item Type:	Article
Status:	Published
Creators/Authors:	Creators Email Pitt Username ORCID Wipf, P pwipf@pitt.edu PWIPF Methot, JL
Date:	3 May 2001
Date Type:	Publication
Journal or Publication Title:	Organic Letters
Volume:	3
Number:	9
Page Range:	1261 - 1263
DOI or Unique Handle:	10.1021/ol0157196
Schools and Programs:	Dietrich School of Arts and Sciences > Chemistry
Refereed:	Yes
ISSN:	1523-7060
MeSH Headings:	Amides--chemistry; Animals; Biological Products--chemistry; Heterocyclic Compounds with 4 or More Rings--chemistry; Molecular Structure; Oxazoles--chemical synthesis; Oxazoles--chemistry; Polymers--chemical synthesis; Polymers--chemistry; Structure-Activity Relationship; Urochordata
Other ID:	10.1021/ol0157196
PubMed ID:	11348209
Date Deposited:	13 Feb 2014 20:07
Last Modified:	02 Feb 2019 15:56
URI:	http://d-scholarship.pitt.edu/id/eprint/20484

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