SYNTHETIC STUDIES IN THE ALKALOID FIELD. X. PREPARATION AND STEREOSTRUCTURE DETERMINATION OF SEVERAL INDOLO (2,3-A) QUINOLIZINE DERIVATIVES
- Author
- LOUNASMAA M; MERIKALLIO H; PUHAKKA M
LAB. CHEM. NATURAL PRODUCTS, ESPOO 02150, FIN - Source
- TETRAHEDRON; GBR; DA. 1978; VOL. 34; NO 19; PP. 2995-2999; BIBL. 17 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- HETEROCYCLE AZOTE HETEROCYCLE AZOTE ANGULAIRE COMPOSE TETRACYCLIQUE STEREOISOMERE REDUCTION REACTION CHIMIQUE SODIUM TETRAHYDROBORATE!ENT ACETIQUE ACIDE!SUB INDOLO (2,3-A) QUINOLIZINEDICARBOXYLIQUE-1,3 ACIDE(OCTAHYDRO-1,2,3,4,6,7,12,12B) ESTER DIMETHYLE!FIN INDOLO (2,3-A) QUINOLIZINEDICARBOXYLIQUE-1,3 ACIDE(HEXAHYDRO-1,2,6,7,12,12B) ESTER DIMETHYLE!FIN!ENT INDOLO (2,3-A) QUINOLIZINEDICARBOXYLIQUE-1,3 ACIDE(OCTAHYDRO-1,2,3,4,6,7,12,12B) ESTER DIMETHYLE,MARQUE D!FIN INDOLO (2,3-A) QUINOLIZINEDICARBOXYLIQUE-1,3 ACIDE (1,2,6,7,12,12B) ESTER DIMETHYLE,MARQUE D!FIN!ENT ALCALOIDE HETEROCYCLE INSATURE CYCLE 2 HETEROATOMES ESTER ESPECE ISOTOPIQUE STRUCTURE MOLECULAIRE DEPLACEMENT CHIMIQUE SOLUTION CHIMIQUE SPECTROMETRIE RMN CARBONE 13 COMPOSE ORGANIQUE CHLOROFORME CHIMIE ORGANIQUE PHYSIQUE MOLECULAIRE PHYSIQUE ATOMIQUE
- Keyword (en)
- NITROGEN HETEROCYCLE ANGULAR NITROGEN HETEROCYCLE TETRACYCLIC COMPOUND STEREOISOMER REDUCTION CHEMICAL REACTION ALKALOID UNSATURATED HETEROCYCLE ESTER ISOTOPIC SPECIES MOLECULAR STRUCTURE CHEMICAL SHIFT CHEMICAL SOLUTION NMR SPECTROMETRY ORGANIC COMPOUNDS ORGANIC CHEMISTRY MOLECULAR PHYSICS ATOMIC PHYSICS
- Keyword (es)
- QUIMICA ORGANICA FISICA MOLECULAR FISICA ATOMICA
- Classification
- Discipline
- Atomic and molecular physics General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL7960194209
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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