Nitrosation of Methyl 2-Cinnamoylamino-3-dimethylamino-propenoates. Alkyl N-Cinnamoyloxalic Acid Hydroxyimidic Amides, Intermediates in the Synthesis of Alkyl 5-Styryl-1,2,4-oxadiazole-3-carboxylates

DOI: 10.1002/jhet.5570340610

Source and publish data:

Journal of Heterocyclic Chemistry p. 1705 - 1708 (1997)

Update date:2022-08-05

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Authors:

Kmetic, Matej

Stanovnik, Branko

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Article abstract of DOI:10.1002/jhet.5570340610

Alkyl 2-(substituted cinnamoylamino)-3-dimethylaminopropenoates 5, prepared either from glycine (1) and substituted cinnamoyl chlorides 2 via oxazol-5(4H)-ones 4, or from cinnamoylglycinate with t-butoxy-bisdimethylaminomethane, were transformed by nitros

Full text of DOI:10.1002/jhet.5570340610

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