The stereoselective synthesis of 4-formyltrinem, a key intermediate for novel trinems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. In vitro activity of the trinem sanfetrinem (GV104326) against gram-positive organisms
2. In vitro activity of the tricyclic beta-lactam GV104326
3. In vitro activity of the tribactam GV104326 against gram-positive, gram-negative, and anaerobic bacteria
4. Stereoselective Synthesis of a Key Intermediate of Sanfetrinem by Means of a Chelated Tin(IV) Enolate
5. The use of zinc enolates in the synthesis of a key intermediate for the preparation of trinem antibiotics
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1. Synthesis, spectroscopic investigation and theoretical studies of 2-((E)-(2-(2-cyanoacetyl)hydrazono)methyl)-4-((E)-phenyldiazenyl)phenyl methyl carbonate;Journal of Molecular Structure;2017-04
2. Synthesis, Spectroscopic Investigation and Computational Studies of 2-Formyl-4-(Phenyldiazenyl)Phenyl Methyl Carbonate and 4-((4-Chlorophenyl)Diazenyl)-2-Formylphenyl Methyl Carbonate;International Letters of Chemistry, Physics and Astronomy;2016-05-30
3. Synthesis, Spectroscopic Investigation and Computational Studies of 2-Formyl-4-(Phenyldiazenyl)Phenyl Methyl Carbonate and 4-((4-Chlorophenyl)Diazenyl)-2-Formylphenyl Methyl Carbonate;International Letters of Chemistry, Physics and Astronomy;2016-05
4. Synthesis of azo carbonate monomers and biocompatibility study of poly(azo-carbonate-urethane)s;RSC Advances;2016
5. Guanidines as Catalysts for Direct and Indirect CO2 Capture and Activation;Topics in Heterocyclic Chemistry;2015
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