A microwave assisted intramolecular-furan-Diels-Alder approach to 4-substituted indoles

Petronijevic, F and Timmons, C and Cuzzupe, A and Wipf, P (2009) A microwave assisted intramolecular-furan-Diels-Alder approach to 4-substituted indoles. Chemical Communications (1). 104 - 106. ISSN 1359-7345

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Abstract

The key steps of a versatile new protocol for the convergent synthesis of 3,4-disubstituted indoles are the addition of an α-lithiated alkylaminofuran to a carbonyl compound, a microwave-accelerated intramolecular Diels-Alder cycloaddition and an in situ double aromatization reaction. © The Royal Society of Chemistry.

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Details

Item Type:	Article
Status:	Published
Creators/Authors:	Creators Email Pitt Username ORCID Petronijevic, F Timmons, C Cuzzupe, A Wipf, P pwipf@pitt.edu PWIPF
Date:	1 January 2009
Date Type:	Publication
Journal or Publication Title:	Chemical Communications
Number:	1
Page Range:	104 - 106
DOI or Unique Handle:	10.1039/b816989f
Schools and Programs:	Dietrich School of Arts and Sciences > Chemistry
Refereed:	Yes
ISSN:	1359-7345
MeSH Headings:	Cyclization; Electrons; Furans--chemistry; Heterocyclic Compounds--chemistry; Indicators and Reagents; Indoles--chemical synthesis; Indoles--radiation effects; Lithium--chemistry; Microwaves
Other ID:	NLM NIHMS140546, NLM PMC2736609
PubMed Central ID:	PMC2736609
PubMed ID:	19082013
Date Deposited:	03 Jul 2013 14:56
Last Modified:	02 Feb 2019 15:57
URI:	http://d-scholarship-dev.library.pitt.edu/id/eprint/19219

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