Iminium Ion Route to Azomethine Ylides from Primary and Secondary Amines

DOI: 10.1039/c39860000602

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 602 - 604 (1986)

Update date:2022-08-04

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Authors:

Ardill, Harriet

Grigg, Ronald

Sridharan, Visuvanathar

Surendrakumar, Sivaguanasundram

Thianpatanagul, Sunit

Kanajun, Saratoon

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Article abstract of DOI:10.1039/c39860000602

Iminium ion formation between primary or secondary amines and carbonyl compounds containing the moiety O=C-C=X results in a facile and stereospecific generation of azomethine ylides which can be trapped in 1,3-dipolar cycloaddition reactions.

Full text of DOI:10.1039/c39860000602

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