A MILD PROCEDURE FOR THE GENERATION OF AZOMETHINE IMINES. STEREOCHEMICAL FACTORS IN THE INTRAMOLECULAR 1,3-DIPOLAR ADDITION OF AZOMETHINE IMINES AND A SYNTHETIC APPROACH TO SAXITOXIN
- Author
- JACOBI PA; BROWNSTEIN A; MARTINELLI M; GROZINGER K
WESLEYAN UNIV., HALL-ATWATER LAB./MIDDLETOWN CT 06457/USA - Source
- J. AM. CHEM. SOC.; ISSN 0002-7863; USA; DA. 1981; VOL. 103; NO 1; PP. 239-241; BIBL. 16 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- REACTION INTRAMOLECULAIRE CYCLOADDITION DIPOLAIRE 1,3 AZOMETHINE IMINE HETEROCYCLE AZOTE ANGULAIRE COMPOSE TRICYCLIQUE HETEROCYCLE SOUFRE DITHIOACETAL CYCLE 5 CHAINONS UREES CYCLE 6 CHAINONS SAXITOXINE DITHIANNE-1,3ACETIQUE-2 ACIDE((OXO-2 IMIDAZOLINE-4YL-4)-2) BENZYL-2P HYDRAZIDE!ENT BENZALDEHYDE,DIETHYLACETAL!ENT PYRROLO IMIDAZO PYRAZOLE DERIVE CHIMIE ORGANIQUE
- Keyword (en)
- INTRAMOLECULAR REACTION 1,3-DIPOLAR CYCLOADDITION AZOMETHINE IMINE ANGULAR NITROGEN HETEROCYCLE TRICYCLIC COMPOUND SULFUR HETEROCYCLE DITHIOACETAL FIVE MEMBERED RING UREAS SIX MEMBERED RING ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL8130375497
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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