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Improved synthesis of structural analogues of (−)-epicatechin gallate for modulation of staphylococcal β-lactam resistance()

The high-yielding synthesis of enantiomerically pure epicatechin gallate analogues where the A and/or B-ring hydroxylation is reduced or altered has been achieved by optimising routes to the catechin stereochemistry. The B-ring analogues were synthesised by using an electrophilic ring closure onto a...

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Bibliografske podrobnosti
Main Authors: Anderson, James C., Grounds, Helen, Reeves, Suzanna, Taylor, Peter W.
Format: Artigo
Jezik:Inglês
Izdano: Pergamon Press 2014
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4006114/
https://ncbi.nlm.nih.gov/pubmed/24876661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2014.03.052
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