Talk:Cefaclor
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reactions of cefachlor with amino acid derivatives such as phthalyl-, tosyl and 1,2,4-triazolyl amino acids using active ester, phosphorous oxy chloride and acid chloride methods to prepare some derivatives with higher antibacterial activities.
Structure image and Name
The structure lacks stereochemistry. The systematic name for this drug is
(6R,7R)-7-{[(2R)-2-amino-2-phenylacetyl]amino}-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid--ChemSpiderMan (talk) 01:26, 19 May 2008 (UTC)
- It also has methyl groups where there should be hydrogens :) I'll let the creator know and replace it with a correct version. Fvasconcellos (t·c) 18:49, 23 August 2008 (UTC)
A Commons file used on this page has been nominated for deletion
The following Wikimedia Commons file used on this page has been nominated for deletion:
Participate in the deletion discussion at the nomination page. —Community Tech bot (talk) 02:01, 3 November 2018 (UTC)