Literature DB >> 21773608

Photodimerisation of glycothymidines in solution and in micelles.

Kirsten Schwekendiek1, Hauke Kobarg, Lena Daumlechner, Frank D Sönnichsen, Thisbe K Lindhorst.   

Abstract

Glycothymidines were designed and synthesized as a new class of functional glycomimetics in which a photochemical [2+2] cycloaddition of the thymine moiety induces structural changes of carbohydrate presentation. To test if photodimerisation of these glycothymidines is feasible within an array of molecules, the photochemical reaction was investigated using NMR and NMR diffusion experiments in solution as well as in the supramolecular context of detergent micelles that mimic cellular membranes. This journal is © The Royal Society of Chemistry 2011

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Year:  2011        PMID: 21773608     DOI: 10.1039/c1cc13246f

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


  2 in total

1.  Synthesis of carbohydrate-scaffolded thymine glycoconjugates to organize multivalency.

Authors:  Anna K Ciuk; Thisbe K Lindhorst
Journal:  Beilstein J Org Chem       Date:  2015-05-07       Impact factor: 2.883

2.  Postsynthetic functionalization of glycodendrons at the focal point.

Authors:  Thisbe K Lindhorst; Katharina Elsner
Journal:  Beilstein J Org Chem       Date:  2014-07-01       Impact factor: 2.883

  2 in total

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