Mechanism of Amine and Amide Ion Substitution Reactions at the Carbon-Nitrogen Double Bond.

DOI: 10.1021/jo00218a021

Source and publish data:

Journal of Organic Chemistry p. 3348 - 3355 (1985)

Update date:2022-08-03

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Authors:

Johnson, James Elver

Ghafouripour, Abdolkarim

Arfan, Mohammad

Todd, Susan L.

Sitz, Deborah A.

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Article abstract of DOI:10.1021/jo00218a021

Reactions of the (Z)-hydroximoyl chlorides 3a-e with secondary amines without solvent at 32 deg C for 24 h give high yields of (Z)-benzamidoximes 7a-f.Although the amidoximes 7a-f do not isomerize under the reaction conditions, they isomerize to the E iso

Full text of DOI:10.1021/jo00218a021

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Article Doi

Mechanism of Amine and Amide Ion Substitution Reactions at the Carbon-Nitrogen Double Bond.

DOI: 10.1021/jo00218a021

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00218a021

Full text of DOI:10.1021/jo00218a021

Products guided by the article

R&D Labs maybe for 97315-85-0

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Benzimidazole condensed ring systems. 2 [1]. New synthesis of substituted 1-oxo-1H,5-H-pyrido[1,2-a]benzimidazole-4-carbonitriles and related derivatives

Ferrocenyl and pyridyl methylenepyrans as potential precursors of organometallic electron-rich extended bipyrans: Synthesis, characterization and crystal structure

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