Literature DB >> 9061202

Convenient chemoenzymatic synthesis of beta-purine-diphosphate sugars (GDP-fucose-analogues).

G Baisch1, R Ohrlein.   

Abstract

A series of peracetylated beta-sugar-1-phosphates with L-fuco configuration are efficiently prepared chemically and coupled in high yields to purine monophosphate bases via imidazolide activation. The resulting purine diphosphate sugars are deacetylated completely by a mild treatment with commercial acetylesterase (EC 3.1.1.6) to give donor-substrates for fucosyl-transferases.

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Year:  1997        PMID: 9061202     DOI: 10.1016/s0968-0896(96)00258-1

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

Review 1.  Substrate and donor specificity of glycosyl transferases.

Authors:  B Ernst; R Oehrlein
Journal:  Glycoconj J       Date:  1999-02       Impact factor: 2.916

2.  Analysis of UDP-D-apiose/UDP-D-xylose synthase-catalyzed conversion of UDP-D-apiose phosphonate to UDP-D-xylose phosphonate: implications for a retroaldol-aldol mechanism.

Authors:  Sei-hyun Choi; Steven O Mansoorabadi; Yung-nan Liu; Tun-Cheng Chien; Hung-wen Liu
Journal:  J Am Chem Soc       Date:  2012-08-15       Impact factor: 15.419

3.  Synthesis of L-ascorbic acid in the phloem.

Authors:  Robert D Hancock; Diane McRae; Sophie Haupt; Roberto Viola
Journal:  BMC Plant Biol       Date:  2003-11-24       Impact factor: 4.215

  3 in total

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