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SYNTHETIC STUDIES ON 8-DEOXYSERRATININE TYPE ALKALOIDS. SELECTIVE CYCLIZATION OF THE 1,2-CYCLOHEXANEDIACETALDEHYDE DERIVATIVE BY INTRAMOLECULAR ALDOL CONDENSATION

Author
HARAYAMA T; TAKATANI M; INUBUSHI Y
KYOTO UNIV., FAC. PHARM. SCI./SAKYO-KU KYOTO/JPN
Source
CHEM. PHARM. BULL.; JPN; DA. 1980; VOL. 28; NO 4; PP. 1276-1286; BIBL. 15 REF.
Document type
Article
Language
English
Keyword (fr)
CYCLISATION REGIOSELECTIVITE PREPARATION REACTION INTRAMOLECULAIRE ALDOLISATION ALCALOIDE SPIRANE ACETAL COMPOSE CHIRAL ETHER EFFET SOLVANT HETEROCYCLE OXYGENE CYCLE 5 CHAINONS ADDITION DIELS ALDER ACETALISATION NAPHTALENONE-1(BENZYLOXY-3P PROPYL-8A METHYL-3 OCTAHYDRO-1,2,3,4,4A,5,8,8A) DIMETHYLENEACETAL!FIN!ENT DIOXA-1,4SPIRO (4.5) DECANEDIACETALDEHYDE-6,7(BENZYLOXY-3P PROPYL-6)!FIN!ENT CYCLOHEXENE-2ONE(ALLYL-2 METHYL-5)!ENT SPIRO (DIOXOLANNE-1,3-2:4P-INDENEACRYLONITRILE-3P)(BENZYLOXY-3S PROPYL-3A' HEXAHYDRO-3A',4P,5P,6P,7P,7A' METHYL-6P)!FIN SPIRO (DIOXOLANNE-1,3-2:7P-INDENEACRYLONITRILE-3P)(BENZYLOXY-3S PROPYL-7A' HEXAHYDRO-3A',4P,5P,6P,7P,7A' METHYL-5P)!FIN ACETONITRILE(DIETHOXYPHOSPHORYL)!ENT DIALDEHYDE PYRROLIDINE PIPERIDINE MORPHOLINE HMPT ETHYLE ETHER PHOSPHONATE ORGANIQUE PHOSPHORE COMPOSE ORGANIQUE CHIMIE ORGANIQUE
Keyword (en)
CYCLIZATION REGIOSELECTIVITY PREPARATION INTRAMOLECULAR REACTION ALDOL CONDENSATION ALKALOID SPIRAN ACETAL CHIRAL COMPOUND ETHER SOLVENT EFFECT OXYGEN HETEROCYCLE FIVE MEMBERED RING DIELS ALDER REACTION ACETALIZATION DIALDEHYDE ORGANIC PHOSPHONATE 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
PASCAL8130107771

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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