Stereoselective synthesis of a building block corresponding to the C(1)-to-C(7) moiety of 14-membered macrolide antibiotics

DOI: 10.1055/s-1991-26485

Source and publish data:

Synthesis p. 435 - 438 (1991)

Update date:2022-08-06

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Born Born

Tamm Tamm

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Article abstract of DOI:10.1055/s-1991-26485

The synthesis of 2',6'-dimethylphenyl (2R,3R,4R,5R,6S)-3-hydroxy-5,7-isopropylidenedioxy-2,4,6-trimethylhepta noate (13) a synthon for the C(1)-to-C(7) segment of a number of 14-membered macrolide antibiotics is described, starting from the meso-diester 3

Full text of DOI:10.1055/s-1991-26485

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Product name:(2S,3R,4R)-5-(tert-butyldiphenylsiloxy)-2,4-dimethylpentane-1,3-diol

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