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- W2000302590 abstract "Hydrazine hydrate, morpholine and benzylamine react with 3-aryl-5-arylmethylene-2,4-dioxothiazolidines 1a–d to give mixtures of thiolopropenamides 2, ethylideneamino-biuret 3 and/or 4-arylaminocarboxamides 4 in varying proportions. However, 3-benzyl-5-arylmethylene 2,4-dioxothiazolidines 1e–f afford mixtures of pyrazolinones 5 and 4-benzyl-hydrazinocarboxamide 6 upon treatment with hydrazine hydrate. The formation of these products is rationalized and discussed on the basis of the role of the substituent at the 3-position. Structures 2–6 have been established." @default.
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- W2000302590 date "1989-01-01" @default.
- W2000302590 modified "2023-09-26" @default.
- W2000302590 title "Studies on 4-thiazolidinones. VIII. The role of substituents at position-3 on the mode of cleavage of 5-Arylmethylene-2,4-dioxothiazolidines" @default.
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- W2000302590 doi "https://doi.org/10.1002/prac.19893310306" @default.
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