4- AND 5-HYDROXYLAMINOTHIAZOLIDINE-2-THIONES. REACTION WITH 4-NITROBENZALDEHYDE

DOI: 10.1007/BF00480846

Source and publish data:

Chemistry of Heterocyclic Compounds p. 433 - 437 (1991)

Update date:2022-09-26

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Authors:

Orlova, T. I.

Epshtein, S. P.

Tashchi, V. P.

Putsykin, Yu. G.

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Article abstract of DOI:10.1007/BF00480846

Stable nitrones are formed in the condensation of 5-hydroxylaminothiazolidine-2-thiones with 4-nitrobenzaldehyde.At the same time, nitrones obtained from the isomeric 4-hydroxylaminothiazolidine-2-thiones, as well as 4-hydroxylaminoimidazolidin-2-one, can undergo rearrengement to E- or Z-O-substituted 4-nitrobenzaldoximes, depending on the structure and the reaction conditions.

Full text of DOI:10.1007/BF00480846

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