INTRAMOLECULAR CYCLIZATIONS OF α-KETOIMIDOYL HALIDES DERIVED FROM ORGANIC ISONITRILES. AN EXPEDIENT APPROACH TO THE SYNTHESIS OF 1-ACYL-3,4-DIHYDROISOQUINOLINES

DOI: 10.1016/S0040-4039(00)98215-7

Source and publish data:

Tetrahedron Letters p. 5389 - 5392 (1985)

Update date:2022-09-26

Topics:

Authors:

Westling, Mark

Livinghouse, Tom

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Article abstract of DOI:10.1016/S0040-4039(00)98215-7

Dihydroisoquinolines are formed in high yield via the cyclization of α-ketoimidoyl halides prepared by the reaction of phenethyl isocyanides with acyl halides.

Full text of DOI:10.1016/S0040-4039(00)98215-7

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