Literature DB >> 15979053

Synthesis of 2,3:4,6-di-O-isopropylidene-D-allopyranose from D-glucose.

Ana M Gómez1, María D Company, Attila Agocs, Clara Uriel, Serafín Valverde, J Cristóbal López.   

Abstract

2,3:4,6-Di-O-isopropylidene-d-allopyranose can be conveniently prepared from d-glucose via a synthetic sequence, which includes Mitsunobu inversion at O-3, di-O-isopropylidenation of phenyl-1-thio-d-alloside and anomeric deprotection on treatment with NBS/CaCO3.

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Year:  2005        PMID： 15979053     DOI： 10.1016/j.carres.2005.05.011

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


  2 in total

1.  Facile Synthesis of Sugar Lactols via Bromine-Mediated Oxidation of Thioglycosides.

Authors:  Shuai Meng; Bishwa Raj Bhetuwal; Padam P Acharya; Jianglong Zhu
Journal:  J Carbohydr Chem       Date:  2019-03-20       Impact factor: 1.667

2.  Stereoselective Synthesis of 2-Azido-2-deoxy-β-d-mannosides via Cs2CO3-Mediated Anomeric O-Alkylation with Primary Triflates: Synthesis of a Tetrasaccharide Fragment of Micrococcus luteus Teichuronic Acid.

Authors:  Bishwa Raj Bhetuwal; Fenglang Wu; Shuai Meng; Jianglong Zhu
Journal:  J Org Chem       Date:  2020-11-17       Impact factor: 4.354
  2 in total

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