DIASTEREOSELECTIVE SYNTHESIS OF OPTICALLY ACTIVE PYRROLIZIDINE AND INDOLIZIDINE RING SYSTEMS THROUGH INTRAMOLECULAR ENE REACTION

DOI: 10.1016/S0040-4039(00)97696-2

Source and publish data:

Tetrahedron Letters p. 4641 - 4644 (1990)

Update date:2022-07-29

Topics:

Authors:

Dike, Suneel Y.

Mahalingam, Murli

Kumar, Ashok

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Article abstract of DOI:10.1016/S0040-4039(00)97696-2

Lewis acid catalyzed diastereoselective intramolecular ene cyclization of optically pure L-proline derived substrates provides asymmetric synthesis of Pyrrolizidine and Indolizidine ring systems.

Full text of DOI:10.1016/S0040-4039(00)97696-2

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Product name:2-Pyrrolidinecarboxaldehyde, 1-(2-methyl-2-propenyl)-, (S)- (9CI)

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