Mixed aryl-alkyl organotin compounds, ArnMeSnCl3-n (Ar = RC6H4, R = H, ethyl, i-propyl, t-butyl; n-hexyl, n-octyl) and the effect of R upon antibiotic activity

Applied Organometallic Chemistry

Volumn 19, Issue 4, 2005, Pages 518-522

  Kapoor, Ramesh N ^a   Apodaca, Paula ^a   Montes, Miguel ^a   Gomez, Fabiola D ^a   Pannell, Keith H ^a  

^a UNIVERSITY OF TEXAS AT EL PASO   (United States)

Author keywords

Arylmethyltin chlorides; Biocide; Hydrophobicity; MIC; Organotin; Synthesis

Indexed keywords

ANTIBIOTICS; CHLORINE COMPOUNDS; COMPLEXATION; HYDROPHOBICITY; SYNTHESIS (CHEMICAL); TIN COMPOUNDS;

BIOLOGICAL ACTIVITY; CHLORIDES; ORGANOTIN COMPOUNDS; TRIARYLMETHYLTIN COMPOUNDS;

ORGANOMETALLICS;

ALKYL GROUP; ANTIBIOTIC AGENT; ETHER; HYDROCHLORIC ACID; METHYLTIN COMPOUND; ORGANOTIN COMPOUND; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG EFFICACY; DRUG STRUCTURE; DRUG SYNTHESIS; GRIGNARD REACTION; HUMAN; HUMAN CELL; HYDROPHOBICITY; MINIMUM INHIBITORY CONCENTRATION; NATURAL KILLER CELL; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STAPHYLOCOCCUS AUREUS; STRUCTURE ANALYSIS;

EID: 16344372674     PISSN: 02682605     EISSN: None     Source Type: Journal    
DOI: 10.1002/aoc.853     Document Type: Article

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