FORMATION OF 4,5-DIHYDRO-1,2,4-TRIAZOLES DURING REARRANGEMENT OF O-ACETYL DERIVATIVES OF 1,2-HYDROXYLAMINOHYDRAZONES AND THIOSEMICARBAZONES

DOI: 10.1007/BF00514996

Source and publish data:

Chemistry of Heterocyclic Compounds p. 287 - 291 (1986)

Update date:2022-07-29

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Authors:

Belova, N. V.

Volodarskii, L. B.

Tikhonov, A. Ya.

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Article abstract of DOI:10.1007/BF00514996

Acylation of phenylhydrazone, semicarbazone, and thiosemicarbazones of 1,2-hydroxylamino-ketones containing a hydroxylamine group at the tertiary carbon atom, by acetic anhydride, leads to products of O-acylation at the hydroxylamine group, which in alkal

Full text of DOI:10.1007/BF00514996

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