Synthesis of erythronolide A via a very efficient macrolactonization under usual acylation conditions with the Yamaguchi reagent

DOI: 10.1016/S0040-4039(00)97066-7

Source and publish data:

Tetrahedron Letters p. 6367 - 6370 (1990)

Update date:2022-08-04

Topics:

Authors:

Hikota Hikota

Sakurai Sakurai

Horita Horita

Yonemitsu

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Article abstract of DOI:10.1016/S0040-4039(00)97066-7

Macrolactonization of 3,5-O-(3,4-dimethoxybenzylidene)-9,11-O-(2,4,6-trimethylbenzylidene)- (9S)-9-dihydroerythronolide A seco-acid (4) was reexamined under various conditions and found to proceed rapidly only by treatment of 4 with Yamaguchi's reagent, 2

Full text of DOI:10.1016/S0040-4039(00)97066-7

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