A facile synthesis of benzyl 2-amino-3-azido-4-O-p-methoxybenzyl-6-O-benzyl-2,3-dideoxy-α-D- glucopyranoside: A key intermediate in the formation of a didemnin B analog

Article abstract of DOI:10.1080/07328309608005660

Although the deprotection of amides by hydrazinolysis is a well established method in carbohydrate chemistry, this reaction is dependent upon the nearby substituents. In our facile synthesis of intermediate benzyl 2-amino-3-azido-4-O-p-methoxybenzyl-6-O-b

Full text of DOI:10.1080/07328309608005660

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A Facile Synthesis of Benzyl 2-Amino-3-
azido-4-O-p-methoxybenzyl-6-O-
benzyl-2,3-dideoxy-α-d-glucopyranoside:
A Key Intermediate in the Formation Of
A Didemnin B Analog
Joshi M. Ramanjulu a & Madeleine M. Joullié a
a Department of Chemistry , University of Pennsylvania ,
Philadelphia, Pennsylvania , 19104-6323
Published online: 22 Aug 2006.
To cite this article: Joshi M. Ramanjulu & Madeleine M. Joullié (1996) A Facile Synthesis of Benzyl 2-
Amino-3-azido-4-O-p-methoxybenzyl-6-O-benzyl-2,3-dideoxy-α-d-glucopyranoside: A Key Intermediate
in the Formation Of A Didemnin B Analog, Journal of Carbohydrate Chemistry, 15:3, 371-381, DOI:
10.1080/07328309608005660
To link to this article: http://dx.doi.org/10.1080/07328309608005660
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