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Reactions of 2-Monosubstituted 3-Amino-2H-azirines with NH-Acidic Heterocycles

Villalgordo, Jose M; Linden, Anthony; Heimgartner, Heinz (1992). Reactions of 2-Monosubstituted 3-Amino-2H-azirines with NH-Acidic Heterocycles. Helvetica Chimica Acta, 75:2270-2282.

Abstract

2-Monosubstituted 3-amino-2H-azirines 2 react with several heterocycles containing acidic NH groups via ring expansions, leading to benzo[g][1,2,5]thiadiazocin 1,1-dioxide derivatives 6 and imidazoles 9, 10, and 13, respectively.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
Dewey Decimal Classification:540 Chemistry
Scopus Subject Areas:Physical Sciences > Catalysis
Life Sciences > Biochemistry
Life Sciences > Drug Discovery
Physical Sciences > Physical and Theoretical Chemistry
Physical Sciences > Organic Chemistry
Physical Sciences > Inorganic Chemistry
Uncontrolled Keywords:Physical and Theoretical Chemistry, Inorganic Chemistry, Organic Chemistry, Biochemistry, Drug Discovery, Catalysis
Language:English
Date:1992
Deposited On:03 Jan 2014 07:06
Last Modified:10 Mar 2025 02:39
Publisher:Wiley-Blackwell
ISSN:0018-019X
Funders:Swiss National Science Foundation, F. Hoffmann-La Roche AG, Basel
OA Status:Closed
Publisher DOI:https://doi.org/10.1002/hlca.19920750713
Project Information:
  • Funder: SNSF
  • Grant ID:
  • Project Title: Swiss National Science Foundation
  • Funder:
  • Grant ID:
  • Project Title: F. Hoffmann-La Roche AG, Basel

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