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Synthesis and Reactions of a 2H-Azirine Unsubstituted on C–3

Bauer, W. ; Hafner, Klaus (1969)
Synthesis and Reactions of a 2H-Azirine Unsubstituted on C–3.
In: Angewandte Chemie International Edition, 8 (10)
doi: 10.1002/anie.196907721
Article, Bibliographie

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Abstract

Thermolysis [¹] or photolysis [²] of 1-alkyl or 1-aryl-vinyl azides (1) (R¹ = R² = H, aryl, alkyl; R³= aryl, alkyl)[³] leads to the formation of 2H-azirines with a substituent at C-3 (2) and to ketenimines (3). However, the decomposition of “terminal” vinyl azides (1) (R¹ = R² == H, aryl, alkyl; R³ = H) gives only the nitriles (4) [⁴] and none of the expected, and formerly unknown, 2H-azirines which lack a substituent at the 3-position.

Item Type: Article
Erschienen: 1969
Creators: Bauer, W. ; Hafner, Klaus
Type of entry: Bibliographie
Title: Synthesis and Reactions of a 2H-Azirine Unsubstituted on C–3
Language: English
Date: 1969
Place of Publication: Darmstadt
Publisher: Wiley
Journal or Publication Title: Angewandte Chemie International Edition
Volume of the journal: 8
Issue Number: 10
DOI: 10.1002/anie.196907721
Corresponding Links:
Abstract:

Thermolysis [¹] or photolysis [²] of 1-alkyl or 1-aryl-vinyl azides (1) (R¹ = R² = H, aryl, alkyl; R³= aryl, alkyl)[³] leads to the formation of 2H-azirines with a substituent at C-3 (2) and to ketenimines (3). However, the decomposition of “terminal” vinyl azides (1) (R¹ = R² == H, aryl, alkyl; R³ = H) gives only the nitriles (4) [⁴] and none of the expected, and formerly unknown, 2H-azirines which lack a substituent at the 3-position.

Classification DDC: 500 Science and mathematics > 540 Chemistry
Divisions: 07 Department of Chemistry
07 Department of Chemistry > Clemens-Schöpf-Institut
07 Department of Chemistry > Clemens-Schöpf-Institut > Organ Chemistry
Date Deposited: 02 Aug 2024 12:45
Last Modified: 02 Aug 2024 12:45
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