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AKTIVIERTE CHINONE: SUBSTITUTION VON AZULENEN, BENZOFURAN UND INDOLEN DURCH 2-METHOXYCARBONYL-1,4-BENZOCHINON. REGIOSPEZIFISCHE SYNTHESEN VON POLYMETHOXY-FLUORENONEN UND EINE NEUE SYNTHESE DES 2,6-DIHYDRONAPHTHO (1,2,3-CD) INDOL-6-ON-SYSTEMS.

Other title
QUINONES ACTIVEES: SUBSTITUTION D'AZULENES, BENZOFURANNES ET INDOLES PAR LA METHOXYCARBONYL-2 BENZOQUINONE-1,4. SYNTHESES REGIOSPECIFIQUES DE POLYMETHOXY FLUORENONES ET NOUVELLE SYNTHESE DU SYSTEME DIHYDRO-2,6 NAPHTO (1,2,3-CD) INDOLONE-6 (fr)
Author
TSAKLIDIS JN; HOFER A; EUGSTER CH
ORG.-CHEM. INST., UNIV. ZUERICH, CH-8001 ZUERICH
Source
HELV. CHIM. ACTA; SUISSE; DA. 1977; VOL. 60; NO 3; PP. 1033-1060; ABS. ANGL.; BIBL. 1 P. 1/2
Document type
Article
Language
German
Keyword (fr)
COMPOSE AROMATIQUE CONDENSE COMPOSE BICYCLIQUE COMPOSE TRICYCLIQUE HETEROCYCLE OXYGENE HETEROCYCLE AZOTE REACTION CHIMIQUE SUBSTITUTION ELECTROPHILE PREPARATION REGIOSPECIFICITE SPECTRE UV SPECTRE VISIBLE SPECTRE RMN AZULENE BENZOFURANNE INDOLE BENZOQUINONE-1,4CARBOXYLIQUE-2 ACIDE,ESTER METHYLE FLUORENONE(POLYMETHOXY) NAPHTOINDOLE(DIHYDRO METHOXY OXO) CHIMIE ORGANIQUE
Keyword (en)
BICYCLIC COMPOUND TRICYCLIC COMPOUND OXYGEN HETEROCYCLE NITROGEN HETEROCYCLE CHEMICAL REACTION ELECTROPHILIC SUBSTITUTION PREPARATION REGIOSPECIFICITY ULTRAVIOLET SPECTRA VISIBLE SPECTRUM NMR SPECTRA AZULENE BENZOFURAN INDOLE ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL7760334151

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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