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DIELECTRIC STUDIES. XXXIII. ESTABLISHMENT OF ACETYL GROUP RELAXATION IN MONO- AND PARA-SUBSTITUTED BENZENE COMPOUNDSFARMER DB; MOUNTAIN PF; WALKER S et al.1973; J. PHYS. CHEM.; U.S.A.; DA. 1973; VOL. 77; NO 5; PP. 714-717; BIBL. 19 REF.Serial Issue

PROTON SHIFT ADDITIVITY AND SUBSTITUENT INTERACTION PARAMETERS.BEISTEL DW; CHAPPELL G; EDWARDS WD et al.1977; J. AMER. CHEM. SOC.; U.S.A.; DA. 1977; VOL. 99; NO 5; PP. 1309-1311; BIBL. 12 REF.Article

FORMATION OF DOUBLY CHARGED IONS IN FIELD IONIZATION MASS SPECTRA OF PARA SUBSTITUTED ACETOPHENONESHELAL AI; ZAHRAN NF.1979; ORG. MASS. SPECTROM.; GBR; DA. 1979; VOL. 14; NO 1; PP. 56-57; BIBL. 6 REF.Article

LIGHT-INDUCED KETALISATION OF PHENACYL HALIDES.DIRANIA MKM; IMSEEH HW.1976; CHEM. AND INDUSTRY; G.B.; DA. 1976; NO 18; PP. 788-789; BIBL. 4 REF.Article

ELECTRODIMERISATION. VI. HYDRODIMERISATION ET HYDROGENALYSE DANS LA REDUCTION ELECTROCHIMIQUE DE QUELQUES ACETOPHENONES ALPHA -SUBSTITUEESANDRIEUX CP; SAVEANT JM.1972; BULL. SOC. CHIM. FR.; FR.; DA. 1972; NO 8; PP. 3281-3290; ABS. ANGL.; BIBL. 24 REF.Serial Issue

PI *-PI SYSTEMS IN THE QUARTZ ULTRAVIOLET ELECTRONIC ABSORPTION SPECTRA OF SOME DI-& TRISUBSTITUTED ACETOPHENONESDEVINDER GUPTA; JAISWAL RMP.1980; INDIAN J. PURE APPL. PHYS.; ISSN 0019-5596; IND; DA. 1980; VOL. 18; NO 5; PP. 332-336; BIBL. 32 REF.Article

CHARGE-TRANSFER QUENCHING OF TRIPLET ALPHA -TRIFLUORO-ACETOPHENONESWAGNER PJ; LAM HMH.1980; J. AMER. CHEM. SOC.; USA; DA. 1980; VOL. 102; NO 12; PP. 4167-4172; BIBL. 34 REF.Article

THE EXCESS ACIDITY METHOD: THE BASICITIES AND RATES AND MECHANISMS OF ENOLIZATION, OF SOME ACETOPHENONES AND ACETONE, IN MODERATELY CONCENTRATED SULFURIC ACIDCOX RA; SMITH CR; YATES K et al.1979; CAN. J. CHEM.; ISSN 0008-4042; CAN; DA. 1979; VOL. 57; NO 22; PP. 2952-2959; ABS. FRE; BIBL. 37 REF.Article

KINETIC SHIFT IN SOME PARA-SUBSTITUTED ACETOPHENONESHELAL AI; ZAHRAN NF.1978; ORG. MASS SPECTROM.; GBR; DA. 1978; VOL. 13; NO 9; PP. 549-550; BIBL. 7 REF.Article

CINETIQUE DE CONDENSATION DU FORMALDEHYDE EN PRESENCE D'AROYLCARBINOLSMOROZOV AA; LEVANEVSKIJ OE.1978; KINET. I KATALIZ.; S.S.S.R.; DA. 1978; VOL. 19; NO 3; PP. 580-583; BIBL. 9 REF.Article

REDUCTION ELECTROCHIMIQUE DE DERIVES DU TYPE C6H5COCH(NHR)C6H5ARMAND J; BOULARES L; SOUCHAY P et al.1973; C.R. ACAD. SCI., C; FR.; DA. 1973; VOL. 276; NO 1; PP. 97-100; BIBL. 7 REF.Serial Issue

KINETICS OF THALLIUM(III) OXIDATION OF AROMATIC KETONESKHANDUAL NC; SATPATHY KK; NAYAK PL et al.1973; PROC. INDIAN ACAD. SCI., A; INDIA; DA. 1973; VOL. 77; NO 4; PP. 163-170; BIBL. 1 P.Serial Issue

SORPTION OF ACETOPHENONE BY SEDIMENTS AND SOILSKHAN A; HASSETT JJ; BANWART WL et al.1979; SOIL SCI.; USA; DA. 1979; VOL. 128; NO 5; PP. 297-302; BIBL. 26 REF.Article

THE TORSIONAL BARRIER IN AROMATIC CARBONYL COMPOUNDS. VI: CARBON-12 AND 1H DNMR STUDY OF PROTONATED ALKYL AND HALOALKYL P-TOLYL KETONES.BARTHELEMY JF; JOST R; SOMMER J et al.1978; ORG. MAGNET. RESON.; GBR; DA. 1978; VOL. 11; NO 9; PP. 443-448; BIBL. 24 REF.Article

ASYMMETRIC REDUCTIONS WITH CHIRAL REAGENTS FROM LITHIUM ALUMINIUM HYDRIDE AND (+)-(2S,3R)-4-DIMETHYLAMINO-3-METHYL-1,2-DIPHENYL-2-BUTANOLYAMAGUCHI S; MOSHER HS.1973; J. ORG. CHEM.; U.S.A.; DA. 1973; VOL. 38; NO 10; PP. 1870-1877; BIBL. 27 REF.Serial Issue

BREVET 2.305.422 (A1) (76 08847). - 26 MARS 1976. PROCEDE DE CARBOXYLATION DE SUBSTRATS ORGANIQUES AVEC DE L'ANHYDRIDE CARBONIQUE.sdPatent

ZWITTERIONISCHE ZWISCHENSTUFEN AUS DER CHINOXALIN-REIHE = INTERMEDIAIRES ZWITTERIONIQUES EN SERIE QUINOXALINEUNGUREANU M; DRUTA I; PETROVANU M et al.1972; AN. STI. UNIV. "AL. I. CUZA", IASI, 1 C; ROMAN.; DA. 1972; VOL. 18; NO 1; PP. 49-55; ABS. ROUM.; BIBL. 6 REF.Serial Issue

STERIC EFFECTS ON ACETYL GROUP RELAXATION.MOUNTAIN PF; WALKER S.1975; ADV. MOLEC. RELAX. PROCESSES; NETHERL.; DA. 1975; VOL. 7; NO 2; PP. 105-111; BIBL. 16 REF.Article

MOLECULES ETHYLENIQUES ET ACETYLENIQUES CONJUGUEES. I. ETUDE POLAROGRAPHIQUE DE CETONES ALPHA ,BETA -ACETYLENIQUES DERIVEES DU BENZOYLACETYLENE ET DU PHENYL-BENZOYLACETYLENEDEGRAND C; GROSJEAN B; COMPAGNON PL et al.1973; BULL. SOC. CHIM. FR.; FR.; DA. 1973; NO PART 2; PP. 281-288; BIBL. 14 REF.Serial Issue

FRIEDEL-CRAFTS ISOMERIZATION OF TETRAMETHYLACETOPHENONESSCHLOSBERG RH; WOODBURY RP.1972; J. ORG. CHEM.; U.S.A.; DA. 1972; VOL. 37; NO 16; PP. 2627-2629; BIBL. 9 REF.Serial Issue

BREVET 2.357.516 (A1) (77 05909). - 1ER MARS 1977. PROCEDE DE PREPARATION DE CETONES HALOGENEES EN ALPHA .sdPatent

STRUCTURE SPATIALE DE CERTAINES ACETOPHENONES OMEGA -SUBSTITUEESARBUZOV BA; LAPKIN II; KHAMATULLINA IM et al.1978; IZVEST. AKAD. NAUK S.S.S.R., SER. KHIM.; S.S.S.R.; DA. 1978; NO 1; PP. 80-84; BIBL. 19 REF.Article

CONDENSATION DU PHENYLGLYOXAL AVEC LE METHYLURETHANNEDRACH BS; DOLGUSHINA I YU; KIRSANOV AV et al.1972; ZH. ORG. KHIM.; S.S.S.R.; DA. 1972; VOL. 8; NO 6; PP. 1224-1227; BIBL. 8 REF.Serial Issue

SPECTRES PHOTOELECTRONIQUES, STRUCTURE ELECTRONIQUE ET GEOMETRIQUE DES PHENYLHYDRAZONESVILESOV FI; VOVNA VI; LOPATIN SN et al.1976; TEOR. EKSPER. KHIM., U.S.S.R.; S.S.S.R.; DA. 1976; VOL. 12; NO 2; PP. 237-241; BIBL. 3 REF.Article

Acetanisole: How this ingredient's hawthorn character helps create interesting, commercial-quality flavorsWRIGHT, John.Perfumer & flavorist. 2012, Vol 37, Num 12, pp 20-21, issn 0272-2666, 2 p.Article

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