The title compound 5 was prepared from the I-P-D-azido-glucose I via four steps. Alternatively, 5 was synthesized from 1, via acetalation, cycloaddition with acetylene derivative, reduction, then carbamoylation followed by an acid hydrolysis. (C) 2002 Elsevier Science Ltd. All rights reserved.
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MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467
LALEZARI, I
GOMEZ, LA
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GOMEZ, LA
KHORSHIDI, M
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MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467
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MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467
LALEZARI, I
GOMEZ, LA
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MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467
GOMEZ, LA
KHORSHIDI, M
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MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT MED,DIV IMMUNOHEMATOL,BRONX,NY 10467