Literature DB >> 15582617

An efficient route to thioglycosides with the 2,3-anhydro-D-ribo stereochemistry.

Jayant N Tilekar1, Todd L Lowary.   

Abstract

An improved route for the synthesis of p-tolyl 2,3-anhydro-5-O-benzoyl-1-thio-beta-D-ribofuranoside and its alpha anomer, which are important intermediates in the synthesis of alpha- and beta-D-arabinofuranosides, has been developed. The products are obtained in six steps from D-xylose in 39% overall yield.

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Year:  2004        PMID: 15582617     DOI: 10.1016/j.carres.2004.10.009

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


  1 in total

1.  Stereocontrolled Synthesis of α-Xylofuranosides Using a Conformationally Restricted Donor.

Authors:  Li Zhang; Ke Shen; Hashem A Taha; Todd L Lowary
Journal:  J Org Chem       Date:  2018-06-26       Impact factor: 4.354

  1 in total

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