FUNCTIONALIZED 2-AZABICYCLONONANES. X. α,α'-ANNELATION OF 1-BENZYL-2,5-PIPERIDINE-DIONE AND ISOLATION OF AN AZABICYCLIC ADDUCT AS STABLE HYDRATE

DOI: 10.1016/S0040-4039(00)99599-6

Source and publish data:

Tetrahedron Letters p. 1861 - 1862 (1989)

Update date:2022-07-30

Topics:

Authors:

Bonjoch, Josep

Quirante, Josefina

Serret, Isabel

Bosch, Joan

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Article abstract of DOI:10.1016/S0040-4039(00)99599-6

The reaction of the pyrrolidine enamine derived from 1-benzyl-2,5-piperidinedione with acrolein afforded a 3,6,9-trifunctionalized 2-azabicyclo<3.3.1>nonane system, which could be isolated as a stable ketone hydrate.

Full text of DOI:10.1016/S0040-4039(00)99599-6

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