Highly stereoselective synthesis of the 1-O-acylglycosyl ester of diclofenac via glycosyl phosphorothioates, -selenoates and -dithioates as glycosyl donors

DOI: 10.1002/jlac.199719971017

Source and publish data:

Liebigs Annalen p. 2147 - 2150 (1997)

Update date:2022-08-03

Topics:: Authors:

Borowiecka, Joanna

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Article abstract of DOI:10.1002/jlac.199719971017

Stereoselective glycosylation of o-(2,6-dichloroanilino)phenylacetic acid (Diclofenac, 1), as a free carboxylic acid with glycosylthio (2a-c), -dithio (3a-e) and -selenophosphates (4a-c) as glycosyl donors is reported. The reactions were carried out in ap

Full text of DOI:10.1002/jlac.199719971017

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Highly stereoselective synthesis of the 1-O-acylglycosyl ester of diclofenac via glycosyl phosphorothioates, -selenoates and -dithioates as glycosyl donors

DOI: 10.1002/jlac.199719971017

Source and publish data:

Authors:

Article abstract of DOI:10.1002/jlac.199719971017

Full text of DOI:10.1002/jlac.199719971017

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