Asymmetric synthesis of orsellinic acid type macrolides: The example of lasiodiplodin

DOI: 10.1016/0957-4166(90)90013-Z

Source and publish data:

Tetrahedron Asymmetry p. 187 - 198 (1990)

Update date:2022-08-04

Topics: Asymmetric synthesis Experimental terms Macrolides Lasiodiplodin

Authors:

Solladie

Rubio Rubio

Carreno Carreno

Ruano Ruano

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Article abstract of DOI:10.1016/0957-4166(90)90013-Z

The asymmetric synthesis of both enantiomers of methyl lasiodiplodin is described. The chiral centers were created in the very last steps of the synthesis by asymmetric induction of a chiral sulfoxide group.

Full text of DOI:10.1016/0957-4166(90)90013-Z

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