An efficient route to regio- and stereoselective synthesis of 3-amino-3-deoxy sugars

DOI: 10.1016/0040-4020(95)00087-O

Source and publish data:

Tetrahedron p. 3141 - 3148 (1995)

Update date:2022-08-05

Topics:

Authors:

Al-Tel, Taleb H.

Al-Qawasmeh, Raed A.

Schroeder, Christoph

Voelter, Wolfgang

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Article abstract of DOI:10.1016/0040-4020(95)00087-O

Starting from the trans-oriented hydroxy-epoxy pentoses (1,8 and 15) and benzoylisocyanate a regio-and stereoselective route via the benzoylcarbamate intermediates 2, 9 and 16 to the 3-amino-3-deoxy sugars 7, 14 and 18 is described.

Full text of DOI:10.1016/0040-4020(95)00087-O

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Product name:Benzoyl-carbamic acid (1S,2S,5R,6S)-2-benzyloxy-3,7-dioxa-bicyclo[4.1.0]hept-5-yl ester

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