Enantioselective synthesis of (-)-indolizidine 239AB [(3R,5S,8aR)-3-butyl-5-(3-hydroxypropyl-octahydroindolizine]

DOI: 10.1016/0957-4166(96)00273-X

Source and publish data:

Tetrahedron Asymmetry p. 2211 - 2212 (1996)

Update date:2022-08-02

Topics:

Authors:

Vo Thanh, Giang

Celerier, Jean-Pierre

Lhommet, Gerard

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Article abstract of DOI:10.1016/0957-4166(96)00273-X

A highly enantioselective synthesis of the indolizidine alkaloid 239AB is described via the diastereoselective reduction of a chiral cyclic β-enamino ester prepared from (S)-pyroglutamic acid.

Full text of DOI:10.1016/0957-4166(96)00273-X

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