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SYNTHETIC REACTIONS USING ISOXAZOLE COMPOUNDS

Author
KASHIMA C
UNIV. TSUKUBA, DEP. CHEM.,IBARAKI 300-31,JPN
Source
HETEROCYCLES; JPN; DA. 1979; VOL. 12; NO 10; PP. 1343-1368; BIBL. 66 REF.
Document type
Article
Language
English
Keyword (fr)
HETEROCYCLE OXYGENE AZOTE CYCLE 5 CHAINONS METHODE MINDO 2 HETEROCYCLE AZOTE CYCLE 6 CHAINONS ECHANGE ISOTOPIQUE SUBSTITUTION ELECTROPHILE MILIEU BASIQUE DECYCLISATION REGIOSELECTIVITE ACTIVATION REACTION CONDENSATION HYDROGENATION CARBONE DIOXYDE!ENT HYDROXYLAMINE!ENT ISOXAZOLE(DIMETHYL-3,5)!FIN ACETYLACETONE!ENT METHANE(IODO)!ENT ISOXAZOLE(ALKYL-5 METHYL-3)!ENT SODIUM AMIDURE!ENT ISOXAZOLEACETIQUE-5 ACIDE(METHYL-2)!FIN BENZOIQUE ACIDE,ESTER METHYLE!ENT ISOXAZOLE(METHYL-3 PHENACYL-5)!FIN BENZALDEHYDE,PHENYLIMINE!ENT ISOXAZOLE(METHYL-3 STYRYL-5)!ENT ISOXAZOLECARBALDEHYDE-5(METHYL-3) OXIME!FIN PENTENE-3ONE-2(AMINO-4)!FIN PYRIDINE(DIACETYL-3,5 DIHYDRO-1,4 DIMETHYL-2,6)!FIN REACTION CATALYTIQUE AMMONIAC!SUB ADDITION NUCLEOPHILE NITROSATION BASE SCHIFF REDUCTION BIRCH TAUTOMERIE CETOENOLIQUE AMINOCETONE ENONE PYRIMIDONE-2(DIHYDRO-1,2 METHYL-4)!FIN CHIMIE ORGANIQUE
Keyword (en)
OXYGEN NITROGEN HETEROCYCLE FIVE MEMBERED RING MINDO 2 METHOD NITROGEN HETEROCYCLE SIX MEMBERED RING ISOTOPE EXCHANGE ELECTROPHILIC SUBSTITUTION BASIC MEDIUM RING CLEAVAGE REGIOSELECTIVITY ACTIVATION HYDROGENATION CATALYTIC REACTION NUCLEOPHILIC ADDITION NITROSATION SCHIFF BASE BIRCH REDUCTION KETO ENOL TAUTOMERISM AMINOKETONE ENONE 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
PASCAL8060182609

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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