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Stereoselective Synthesis of a Tetrasaccharide Phosphate in the Linkage Region of the Arabinogalactan-Peptidoglycan Complex in Mycobacterial Cell Wall

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영어

Synthesis of dibenzyl (6-O-naphtylmethyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl)- (1→5)-(2,3-di-O-benzoyl-6-O-benzyl-β-D-galactofuranosyl)-(1→4)-(3-O-benzyl-2- O-pivaloyl-α-L-rhamnopyranosyl)-(1→3)-2-acetamido-2-deoxy-4,6-di-O-benzoyl-α -D-glucopyranosyl phosphate (A), a protected form of the tetrasaccharide phosphate of the linkage region of the arabinogalactan-peptidoglycan complex in mycobacterial cell wall, has been accomplished. Key steps include the coupling of four monosaccharide building blocks with complete stereoselectivity by glycosylations employing thioglycosides, 2'–carboxybenzyl glycosides, and glycosyl fluorides as glycosyl donors. The α-glycosyl phosphate linkage was also stereoselectively elaborated by reaction of a tetrasaccharide hemiacetal with tetrabenzyl pyrophosphate in the presence of a base.

저자정보

  • Dinanath B.Fulse Center for Bioactive Molecular Hybrids, Department of Chemistry, Yonsei University
  • Ju Yuel Baek Center for Bioactive Molecular Hybrids, Department of Chemistry, Yonsei University
  • Kwan Soo Kim Center for Bioactive Molecular Hybrids, Department of Chemistry, Yonsei University

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