The Mechanism of Cyclization of 1,4-Diaryl-1-azido-2,3-diazabuta-1,3-dienes to Tetrazoles. Imidoyl Azides stabilized by Slow Nitrogen Inversion

DOI: 10.1039/P29800000535

Source and publish data:

Journal of the Chemical Society. Perkin transactions II p. 535 - 540 (1980)

Update date:2022-08-05

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Authors:

Hegarty, Anthony F.

Brady, Kieran

Mullane, Maria

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Article abstract of DOI:10.1039/P29800000535

The imidoyl azides (9) are stabilized in the open chain azido form because of their configuration (which is Z about the C=N bond) and slow ZE isomerization.The rates of conversion of the azides (9) into the isomeric tetrazoles (12) have been measused and

Full text of DOI:10.1039/P29800000535

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