Literature DB >> 21853169

De novo synthesis of deoxy sugar via a Wharton rearrangement.

Hua-Yu Leo Wang1, George A O'Doherty.   

Abstract

A highly divergent synthesis of α-fuco-, α-6-deoxy-allo-, α-6-deoxy-altro-pyranosides has been achieved. This route utilizes a Wharton rearrangement as part of a new post-glycosylation transformation strategy. This journal is © The Royal Society of Chemistry 2011

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Year:  2011        PMID： 21853169     DOI： 10.1039/c1cc13837e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  4 in total

1.  Rapid de Novo Preparation of 2,6-Dideoxy Sugar Libraries through Gold-Catalyzed Homopropargyl Orthoester Cyclization.

Authors:  Subbarao Yalamanchili; William Miller; Xizhao Chen; Clay S Bennett
Journal:  Org Lett       Date:  2019-11-22       Impact factor: 6.005

2.  From d- to l-Monosaccharide Derivatives via Photodecarboxylation-Alkylation.

Authors:  I C Steven Wan; Martin D Witte; Adriaan J Minnaard
Journal:  Org Lett       Date:  2019-09-12       Impact factor: 6.005

3.  An efficient and scalable synthesis of 2,4-di-N-acetyl-l-altrose (l-2,4-Alt-diNAc).

Authors:  Anna Niedzwiecka; Carita Sequeira; Ping Zhang; Chang-Chun Ling
Journal:  RSC Adv       Date:  2021-03-19       Impact factor: 3.361

4.  Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans.

Authors:  Olena P Ishchuk; Olov Sterner; Ulf Ellervik; Sophie Manner
Journal:  Antibiotics (Basel)       Date:  2019-12-30
  4 in total

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