TY - JOUR
T1 - Glycosylation with 2′-carboxybenzyl glycosides as glycosyl donors
T2 - Scope and application to the synthesis of a tetrasaccharide
AU - Kim, Kwan Soo
AU - Kang, Sung Soo
AU - Seo, Yong Sung
AU - Kim, Hyo Jin
AU - Lee, Yong Joo
AU - Jeong, Kyu Sung
PY - 2003
Y1 - 2003
N2 - Glycosylation of 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside (3), CB 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside (4), and CB 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside (5) as glycosyl donors with various glycosyl acceptors provided corresponding disaccharides in high yields. The present CB glycoside methodology was successfully applied to the efficient construction of the tetrasaccharide 41.
AB - Glycosylation of 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside (3), CB 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside (4), and CB 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside (5) as glycosyl donors with various glycosyl acceptors provided corresponding disaccharides in high yields. The present CB glycoside methodology was successfully applied to the efficient construction of the tetrasaccharide 41.
UR - http://www.scopus.com/inward/record.url?scp=0038442297&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0038442297&partnerID=8YFLogxK
U2 - 10.1055/s-2003-40348
DO - 10.1055/s-2003-40348
M3 - Article
AN - SCOPUS:0038442297
SN - 0936-5214
SP - 1311
EP - 1314
JO - Synlett
JF - Synlett
IS - 9 SPEC. ISS.
ER -