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A NOVEL METHOD FOR THE SYNTHESIS OF 2,2,2-TRIBROMOETHANOLS FROM ALDEHYDES AND CARBONATETRABROMIDE IN THE PRESENCE OF STANNOUS FLUORIDE. A SYNTHESIS OF DIACETYL-D-ERYTHRONOLACTONE

Author
MUKAIYAMA T; YAMAGUCHI M; KATO JI
UNIV. TOKYO, FAC. SCI., DEP. CHEM./BUNKYO-KU TOKYO 113/JPN
Source
CHEM. LETT.; ISSN 0366-7022; JPN; DA. 1981; NO 10; PP. 1505-1508; BIBL. 13 REF.
Document type
Article
Language
English
Keyword (fr)
ETAIN II FLUORURE!ACT ALDEHYDE STEREOSELECTIVITE STEREOISOMERE D REACTION CHIMIQUE ALCOOL SECONDAIRE COMPOSE BENZENIQUE HETEROCYCLE OXYGENE CYCLE 5 CHAINONS COMPOSE ALIPHATIQUE COMPOSE SATURE COMPOSE ALLYLIQUE CETOL HALOGENOCETONE COMPOSE VINYLIQUE CETOALDEHYDE ACIDE ALDONIQUE BENZALDEHYDE!ENT FURFURAL!ENT ETHANOL(PHENYL-1 TRIBROMO-2,2,2)!FIN FURYLIQUE ALCOOL(ALPHA -TRIBROMOMETHYL)!FIN BUTANOL-2(PHENYL-4 TRIBROMO-1,1,1)!FIN BUTENE-3OL-2(PHENYL-4 TRIBROMO-1,1,1)!FIN PROPIOPHENONE(HYDROXY-2 TRIBROMO-3,3,3)!FIN CINNAMALDEHYDE!ENT PHENYLGLYOXAL!ENT ERYTHRONIQUE ACIDE(DI-O-ACETYL) LACTONE-1(4)!FIN DIOXOLANNE-1,3CARBALDEHYDE-4(DIMETHYL-2,2)!ENT METHANE(TETRABROMO)!ENT DMSO!SUB SPECTRE IR SPECTRE RMN BENZENE ACETIQUE ACIDE(ALPHA -ACETOXY)!FIN HYDROXYACIDE MANDELIQUE ACIDE DERIVE HALOGENOALCOOL HYDROGENE 1 CARBONE 13 CHIMIE ORGANIQUE
Keyword (en)
TIN II FLUORIDES!ACT ALDEHYDE STEREOSELECTIVITY D STEREOISOMER CHEMICAL REACTION SECONDARY ALCOHOL BENZENIC COMPOUND OXYGEN HETEROCYCLE FIVE MEMBERED RING ALIPHATIC COMPOUND SATURATED COMPOUND ALLYLIC COMPOUND KETOL HALOKETONE VINYLIC COMPOUND KETOALDEHYDE ALDONIC ACID BENZALDEHYDE!ENT 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
PASCAL82X0056231

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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