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A THEORETICAL INVESTIGATION OF THE STRUCTURE AND ROTATIONAL BARRIERS OF PEROXYFORMIMIDIC ACID. THE MECHANISM OF STEREOMUTATION AT THE CARBON-NITROGEN DOUBLE BOND

Author
LANG TJ; WOLBER GJ; BACH RD
WAYNE STATE UNIV., DEP. CHEM./DETROIT MI 48202/USA
Source
J. AM. CHEM. SOC.; ISSN 0002-7863; USA; DA. 1981; VOL. 103; NO 12; PP. 3275-3282; BIBL. 22 REF.
Document type
Article
Language
English
Keyword (fr)
BARRIERE ROTATION CONFORMATION ANGLE LIAISON ETUDE THEORIQUE METHODE MO METHODE AB INITIO BARRIERE INVERSION EPOXYDATION ALCENE REACTION CHIMIQUE ISOMERISATION CIS-TRANS INVERSION AZOTE ROTATION INTERNE PERACIDE CARBOXYLIQUE PERFORMIMIDIQUE ACIDE!ENT ORBITALE GAUSSIENNE ACIDE CARBOXIMIDIQUE COMPOSE ORGANIQUE DIMENSION BASE CHIMIE ORGANIQUE PHYSIQUE MOLECULAIRE PHYSIQUE ATOMIQUE
Keyword (en)
ROTATION BARRIER CONFORMATION BOND ANGLE THEORETICAL STUDY MO METHOD AB INITIO METHOD INVERSION BARRIER EPOXIDATION ALKENE CHEMICAL REACTION CIS TRANS ISOMERIZATION NITROGEN INVERSION INTERNAL ROTATION PERCARBOXYLIC ACID ORGANIC CHEMISTRY MOLECULAR PHYSICS ATOMIC PHYSICS
Keyword (es)
QUIMICA ORGANICA FISICA MOLECULAR FISICA ATOMICA
Classification
Pascal
001 Exact sciences and technology / 001B Physics / 001B30 Atomic and molecular physics

Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry

Discipline
Atomic and molecular physics Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL82X0062540

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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