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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/18335

Title: New routes towards reutericyclin analogues
Authors: Jones, Raymond C.F.
Bullous, James P.
Law, Carole C.M.
Elsegood, Mark R.J.
Issue Date: 2014
Publisher: © Royal Society of Chemistry
Citation: JONES, R.C.F. ... et al, 2014. New routes towards reutericyclin analogues. Chemical Communications, 50 (13), pp.1588-1590
Abstract: A range of N-acylpyrrolo[3,4-c]isoxazoles and derived N-5 acyltetramides has been prepared via a nitrile oxide dipolar cycloaddition approach, as analogues of the acyltetramic acid metabolite reutericyclin, of interest for their antibiotic potential against Gram-positive bacteria including hospital-acquired infections of resistant Clostridium difficile.
Description: This paper was submitted for publication in the journal Chemical Communications. The definitive version can be found at: http://dx.doi.org/10.1039/c3cc47867j
Version: Submitted for publication
DOI: 10.1039/c3cc47867j
URI: https://dspace.lboro.ac.uk/2134/18335
Publisher Link: http://dx.doi.org/10.1039/c3cc47867j
ISSN: 1359-7345
Appears in Collections:Published Articles (Chemistry)

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