FUNCTIONALIZED CHLOROENAMINES IN AMINOCYCLOPROPANE SYNTHESIS-II. TRICYCLIC AMIDINES FROM CARBAMOYLATED CHLOROENAMINES

DOI: 10.1016/0040-4020(89)80040-7

Source and publish data:

Tetrahedron p. 131 - 140 (1989)

Update date:2022-08-05

Topics:

Authors:

Vilsmaier, Elmar

Adam, Rainer

Altmeier, Peter

Cronauer, Regina

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Article abstract of DOI:10.1016/0040-4020(89)80040-7

Tricyclic amidines 9a-d were obtained from the reaction of cyanide with carbamoylated chloroenamines 2a-d at room temperature.At elevated temperatures the rearranged amidine 10a was the reaction product from 2a and cyanide.Rearranged amidines 10a-c also w

Full text of DOI:10.1016/0040-4020(89)80040-7

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