PYRROLIDINES BY INTRAMOLECULAR ADDITION OF KOLBE RADICALS GENERATED FROM β-ALLYLAMINOALKANOATES

DOI: 10.1016/0040-4039(88)85212-2

Source and publish data:

Tetrahedron Letters p. 2797 - 2800 (1988)

Update date:2022-08-04

Topics:

Authors:

Becking, L.

Schaefer, H. J.

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Article abstract of DOI:10.1016/0040-4039(88)85212-2

3-Alkyl-substituted pyrrolidines 7 are obtained by Kolbe electrolysis of β-llylaminoalkanoates 5, intramolecular addition of the radical nd mixed coupling with the radical of a coacid.

Full text of DOI:10.1016/0040-4039(88)85212-2

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