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.
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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.
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.
Item Type: | Journal Article, refereed, original work |
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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: |
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