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
[edit]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
[edit]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)
