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ALPHA -AMINOSAEUREN ALS NUCLEOPHILE ACYLAEQUIVALENTE. IV: SYNTHESE SYMMETRISCHER KETONE UNTER VERWENDUNG VON 2-PHENYL-2-OXAZOLIN-5-ON

Other title
ALPHA -AMINOACIDES COMME EQUIVALENT ACYLE NUCLEOPHILE. IV. SYNTHESE DE CETONES SYMMETRIQUES A PARTIR DE PHENYL-2 OXAZOLINE-2ONE-5 (fr)
Author
LOHMAR R; STEGLICH W
UNIV. BONN, INST. ORGAN. CHEM. BIOCHEM./BONN 5300/DEU
Source
CHEM. BER.; ISSN 0009-2940; DEU; DA. 1980; VOL. 113; NO 12; PP. 3706-3715; ABS. ENG; BIBL. 11 REF.
Document type
Article
Language
German
Keyword (fr)
ALPHA -AMINOACIDE COMPOSE ALIPHATIQUE COMPOSE ALLYLIQUE COMPOSE MONOCYCLIQUE CETOETHER ENOL ETHER OXYDATION MONOTERPENE ANHYDRIDE ORGANIQUE HETEROCYCLE OXYGENE AZOTE CYCLE 5 CHAINONS ALKYLATION HETEROCYCLE OXYGENE HYDROLYSE NONADIENE-2,7ONE-5(DIMETHYL-2,8)!FIN HEPTADIENE-2,5ONE-4(DIMETHYL-2,6)!FIN HEPTADIENE-2,5ONE-4(DIPHENYL-1,7)!FIN INDANONE-2!FIN NONADIENE-2,7DIOIQUE ACIDE DIETHOXY-3,7 OXO-5) ESTER DIETHYLE!FIN CETONE(DI-(CYCLOHEPTATRIENE-2,4,6 YL))!FIN HIPPURIQUE ACIDE!ENT OXAZOLINE-2ONE-5(PHENYL-2)!FIN!ENT HIPPURIQUE ACIDE(DIALKYL-2,2)!FIN!ENT ACETONE(DI-(FURYL-2)-1,3)!FIN PLUMBANE(TETRAACETOXY)!ENT DMF!SUB AMINE(DIETHYL ISOPROPYL)!ACT ALCENE-2(HALOGENO-1)!ENT CHIMIE ORGANIQUE
Keyword (en)
ALIPHATIC COMPOUND ALLYLIC COMPOUND MONOCYCLIC COMPOUND KETOETHER ENOL ETHER OXIDATION MONOTERPENE ORGANIC ANHYDRIDE OXYGEN NITROGEN HETEROCYCLE FIVE MEMBERED RING ALKYLATION OXYGEN HETEROCYCLE HYDROLYSIS 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
PASCAL8130211765

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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