A HIGHLY STEREOSELECTIVE ROUTE TO 1-C-(2-HYDROXYARYL)-ALDITOL DERIVATIVES

DOI: 10.1016/0008-6215(89)84035-2

Source and publish data:

Carbohydrate Research p. 207 - 216 (1989)

Update date:2022-07-29

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Authors:

Casiraghi, Giovanni

Cornia, Mara

Fava, Giovanna Gasparri

Belicchi, Marisa Ferrari

Zetta, Lucia

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Article abstract of DOI:10.1016/0008-6215(89)84035-2

Arylation at C-1 of 2,3:4,5-di-O-isopropylidene-D-arabinose and 4-O-benzyl-2,3-O-isopropylidene-D-threose variously using titanium or magnesium salts of 4-tert-butylphenol, 2-naphthol, and 5-pentylresorcinol gave the epimeric 1-C-arylalditol derivatives.O

Full text of DOI:10.1016/0008-6215(89)84035-2

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Product name:1-C-(3-tert-butyl-6-hydroxyphenyl)-2,3:4,5-di-O-isopropylidene-D-gluco-pentitol

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