Literature DB >> 1797406

Hydrogen fluoride-mediated synthesis of 1-thiotrehaloses involving reaction of D-glucose with hydrogen sulfide.

J Defaye1, A Gadelle, C Pedersen.   

Abstract

Hydrogen sulfide reacted with D-glucose in hydrogen fluoride solution to yield preponderantly alpha,alpha-1-thiotrehalose, beta,beta-1-thiotrehalose, and the alpha,beta anomer. Conditions were found under which the thiotrehaloses were obtained in the respective proportions of 8:5:5.

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Year:  1991        PMID: 1797406     DOI: 10.1016/0008-6215(91)84116-v

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  2 in total

1.  Direct, stereoselective thioglycosylation enabled by an organophotoredox radical strategy.

Authors:  Peng Ji; Yueteng Zhang; Feng Gao; Fangchao Bi; Wei Wang
Journal:  Chem Sci       Date:  2020-10-19       Impact factor: 9.825

2.  Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols.

Authors:  Tamashree Ghosh; Abhishek Santra; Anup Kumar Misra
Journal:  Beilstein J Org Chem       Date:  2013-05-22       Impact factor: 2.883

  2 in total

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