Literature DB >> 20441188

Amino-acid templated assembly of sucrose-derived macrocycles.

Bartosz Lewandowski1, Slawomir Jarosz.   

Abstract

C(2)-Symmetrical chiral macrocycles containing two sucrose units were prepared by an amino acid templated macrocyclization reaction between appropriate sucrose-based linear precursors and ethylenediamine.

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Year:  2010        PMID： 20441188     DOI： 10.1021/ol100749m

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


  3 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.  Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides.

Authors:  Perumal Prabhakaran; Perumal Rajakumar
Journal:  RSC Adv       Date:  2020-03-10       Impact factor: 4.036

3.  Synthesis of a sucrose dimer with enone tether; a study on its functionalization.

Authors:  Zbigniew Pakulski; Norbert Gajda; Magdalena Jawiczuk; Jadwiga Frelek; Piotr Cmoch; Sławomir Jarosz
Journal:  Beilstein J Org Chem       Date:  2014-05-28       Impact factor: 2.883
  3 in total

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