Literature DB >> 22853688

Short synthesis of diamide-linked sucrose macrocycles.

Mykhaylo A Potopnyk1, Piotr Cmoch, Sławomir Jarosz.   

Abstract

A convenient route to macrocyclic diamide-linked macrocyclic derivatives with a sucrose scaffold is presented. Reaction of sucrose based amines (o- and m-) with acid dichlorides afforded the monomeric macrocycles in excellent yields, while reaction of the p-amines also provided dimeric products.

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Year:  2012        PMID: 22853688     DOI: 10.1021/ol301993d

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  An efficient synthesis of novel sucrose-containing dilactams.

Authors:  Mykhaylo A Potopnyk; Sławomir Jarosz
Journal:  Monatsh Chem       Date:  2013-01-17       Impact factor: 1.451

2.  Synthesis of a sucrose-based macrocycle with unsymmetrical monosaccharides "arms".

Authors:  Karolina Tiara; Mykhaylo A Potopnyk; Sławomir Jarosz
Journal:  Beilstein J Org Chem       Date:  2018-03-15       Impact factor: 2.883

3.  De novo macrolide-glycolipid macrolactone hybrids: Synthesis, structure and antibiotic activity of carbohydrate-fused macrocycles.

Authors:  Richard T Desmond; Anniefer N Magpusao; Chris Lorenc; Jeremy B Alverson; Nigel Priestley; Mark W Peczuh
Journal:  Beilstein J Org Chem       Date:  2014-09-17       Impact factor: 2.883

4.  An efficient synthesis of a C12-higher sugar aminoalditol.

Authors:  Łukasz Szyszka; Anna Osuch-Kwiatkowska; Mykhaylo A Potopnyk; Sławomir Jarosz
Journal:  Beilstein J Org Chem       Date:  2017-10-16       Impact factor: 2.883

  4 in total

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