Tautomerism and acidic properties of N-unsubstituted benzohydroxamic acids: Semiempirical quantum chemical estimation

Journal of Structural Chemistry

Volumn 44, Issue 2, 2003, Pages 297-300

  Surova, T V ^a   Enyashin, A N ^a  

^a URAL FEDERAL UNIVERSITY   (Russian Federation)

Author keywords

Acid base properties; AM1 method; N unsubstituted benzohydroxamic acids; Tautomerism

Indexed keywords

BENZOHYDROXAMIC ACID; PHENOL DERIVATIVE;

ACIDITY; AQUEOUS SOLUTION; ARTICLE; COMPUTER PROGRAM; CONFIDENCE INTERVAL; CORRELATION ANALYSIS; DISSOCIATION CONSTANT; EMPIRICISM; GAS; GEOMETRY; ISOMERISM; MATHEMATICAL COMPUTING; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; MOLECULAR MECHANICS; PARAMETER; PHASE TRANSITION; PROBABILITY; QUANTUM CHEMISTRY; REACTION ANALYSIS; REACTION OPTIMIZATION; RING OPENING; STANDARD; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; TECHNIQUE;

EID: 0042377237     PISSN: 00224766     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1025515227844     Document Type: Article

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