From plant to probe: semi-synthesis of labelled undecaprenol analogues allows rapid access to probes for antibiotic targets-Reference-Cited by-同舟云学术

From plant to probe: semi-synthesis of labelled undecaprenol analogues allows rapid access to probes for antibiotic targets

Published:2020 Issue:61 Volume:56 Page:8603-8606
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Cochrane Rachel V. K.¹²³⁴^ORCID,Alexander Francesca M.¹²³⁴,Boland Coilín⁵⁶⁷⁸⁹,Fetics Susan K.⁵⁶⁷⁸⁹,Caffrey Martin⁵⁶⁷⁸⁹^ORCID,Cochrane Stephen A.¹²³⁴^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Queen's University Belfast

3. Belfast

4. UK

5. School of Medicine and School of Biochemistry and Immunology

6. Trinity Biomedical Sciences Institute

7. Trinity College Dublin

8. Dublin 2

9. Ireland

Abstract

Extraction of undecaprenol from bay leaves followed by synthetic modification is a convenient method to obtain novel chemical probes.

Funder

Engineering and Physical Sciences Research Council

Science Foundation Ireland

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/D0CC03388J

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4. The Sweet Tooth of Bacteria: Common Themes in Bacterial Glycoconjugates

5. Protein glycosylation in bacteria: sweeter than ever

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