Glycosylation with 2′-carboxybenzyl glycosides as glycosyl donors: Scope and application to the synthesis of a tetrasaccharide

Kwan Soo Kim, Sung Soo Kang, Yong Sung Seo, Hyo Jin Kim, Yong Joo Lee, Kyu Sung Jeong

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)1311-1314
Number of pages4
JournalSynlett
Issue number9 SPEC. ISS.
Publication statusPublished - 2003 Jul 28

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Glycosylation
Disaccharides
Mannose
Glycosides
benzyl glucopyranoside

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Kim, Kwan Soo ; Kang, Sung Soo ; Seo, Yong Sung ; Kim, Hyo Jin ; Lee, Yong Joo ; Jeong, Kyu Sung. / Glycosylation with 2′-carboxybenzyl glycosides as glycosyl donors : Scope and application to the synthesis of a tetrasaccharide. In: Synlett. 2003 ; No. 9 SPEC. ISS. pp. 1311-1314.
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Glycosylation with 2′-carboxybenzyl glycosides as glycosyl donors : Scope and application to the synthesis of a tetrasaccharide. / Kim, Kwan Soo; Kang, Sung Soo; Seo, Yong Sung; Kim, Hyo Jin; Lee, Yong Joo; Jeong, Kyu Sung.

In: Synlett, No. 9 SPEC. ISS., 28.07.2003, p. 1311-1314.

Research output: Contribution to journalArticle

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AU - Jeong, Kyu Sung

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