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THE EFFECT OF MOLECULAR STRUCTURE ON OPTICAL PROPERTIES OF SYSTEMS CONTAINING CARBON CHIRALITY CENTERS. XIX: SYNTHESIS, SPATIAL CONFIGURATION AND OPTICAL PROPERTIES OF ALPHA -(7,1-BROMONAPHTHYL)-PROPIONIC ACIDS

Author
JANCZEWSKI M; JABLONSKA PIKUS T
M. CURIE-SKLODOWSKA UNIV., INST. CHEM./LUBLIN 20614/POL
Source
POLISH J. CHEM.; POL; DA. 1980; VOL. 54; NO 6; PP. 1155-1169; ABS. POL; BIBL. 12 REF.
Document type
Article
Language
English
Keyword (fr)
RACEMIQUE COMPOSE BICYCLIQUE COMPOSE AROMATIQUE CONDENSE DEDOUBLEMENT OPTIQUE ENANTIOMERE PROPRIETE OPTIQUE DISPERSION ROTATOIRE OPTIQUE EFFET STRUCTURE CONFIGURATION COMPOSE AROMATIQUE COMPOSE ALIPHATIQUE COMPOSE SATURE HALOGENOCETONE ACIDE CARBOXYLIQUE REACTION REFORMATSKY NAPHTALENONE-1(BROMO-7 TETRAHYDRO-1,2,3,4)!ENT PROPIONIQUE ACIDE((BROMO-7 NAPHTYL-1)-2)!FIN PROPIONIQUE ACIDE(BROMO-2) ESTER METHYLE!ENT PROPIONIQUE ACIDE((BROMO-7 NAPHTYL-1)-2) AMIDE!FIN PROPIONIQUE ACIDE((BROMO-7 NAPHTYL-1)-2) ESTER NITRO-4 BENZYLE!FIN PROPIONIQUE ACIDE((BROMO-7 NAPHTYL-1)-2) ESTER BROMO-4 PHENACYLE!FIN CARBOXAMIDE COMPOSE BENZENIQUE CHIRALITE CHIMIE ORGANIQUE
Keyword (en)
RACEMATE BICYCLIC COMPOUND OPTICAL RESOLUTION ENANTIOMER OPTICAL PROPERTIES OPTICAL ROTATORY DISPERSION STRUCTURE EFFECT CONFIGURATION AROMATIC COMPOUND ALIPHATIC COMPOUND SATURATED COMPOUND HALOKETONE CARBOXYLIC ACID REFORMATSKY REACTION CARBOXAMIDE BENZENIC COMPOUND CHIRALITY ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL8130096265

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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