A new diastereoselective route to 5-substituted-8-methylindolizidines. Synthesis of indolizidine (-) 209B

DOI: 10.1016/S0040-4039(98)01040-5

Source and publish data:

Tetrahedron Letters p. 5189 - 5192 (1998)

Update date:2022-07-29

Topics:

Authors:

Bardou, Anita

Celerier, Jean-Pierre

Lhommet, Gerard

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Article abstract of DOI:10.1016/S0040-4039(98)01040-5

The highly diastereoselective synthesis of the indolizidine alkaloid (- ) 209B is described via the diastereoselective alkylation of a chiral cyclic β-amino ester prepared from (R)-methylbenzylamine.

Full text of DOI:10.1016/S0040-4039(98)01040-5

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