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kw.\*:("ISOQUINOLEINE(TETRAHYDRO-1,2,3,4)")

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2.119.989 (B) (7145781). - 20DECEMBRE 1971. PROCEDE DE PREPARATION DE DERIVES DE 1, 2, 3, 4-TETRAHYDROISOQUINOLEINE ET NOUVEAUX PRODUITS AINSI OBTENUS A ACTIVITE DE RELAXATION SUR LES MUSCLES LISSESsdPatent

2.134.047 (B) (7214318). - 21AVRIL 1972. NOUVELLES 1,2,3,4-TETRAHYDROISOQUINOLEINES ET LEUR PROCEDE DE PREPARATIONsdPatent

SYNTHESIS AND HYPOTENSIVE PROPERTIES OF TETRAHYDROISOQUINOLINESMATHISON IW; FOWLER KC; MORGAN PH et al.1973; J. MEDICIN. CHEM.; U.S.A.; DA. 1973; VOL. 16; NO 4; PP. 332-336; BIBL. 6REF.Serial Issue

1,1-DISUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES FROM ISOQUINOLINESNATSUME M; KUMADAKI S; KIUCHI K et al.1972; CHEM. PHARM. BULL.; JAP.; DA. 1972; VOL. 20; NO 7; PP. 1592-1595; BIBL. 6 REF.Serial Issue

3,4-DIHYDROISOCARBOSTYRIL AND 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVE OF EPHEDRINETREPANIER DL; SUNDER S.1973; J. MEDICIN. CHEM.; U.S.A.; DA. 1973; VOL. 16; NO 4; PP. 342-347; BIBL. 10REF.Serial Issue

6,7-DIHYDROXYTETRAHYDROISOQUINOLINE: EVIDENCE FOR IN VIVO INHIBITION OF INTRANEURONAL MONOAMINE OXIDASE. = 6,7-DIHYDROXYTETRAHYDROISOQUINOLINE: PREUVE D'UNE INHIBITION IN VIVO DE LA MONOAMINE OXYDASE INTRANEURONALECOHEN G; KATZ S.1975; J. NEUROCHEM.; G.B.; DA. 1975; VOL. 25; NO 5; PP. 719-722; BIBL. 28 REF.Article

EFFECT OF TETRAHYDROISOQUINOLINE DERIVATIVES ON THE ADENYLATE CYCLASES OF THE CAUDATE NUCLEUS (DOPAMINE TYPE) AND ERYTHROCYTE (BETA -TYPE) OF THE RAT = EFFET DE DERIVES DE LA TETRAHYDROISOQUINOLEINE SUR L'ADENYLATE-CYCLASE DU NOYAU CAUDE (TYPE DOPAMINIQUE) ET DES ERYTHROCYTES (TYPE BETA ) DU RATSHEPPARD H; BURGHARDT CR.1974; RES. COMMUNIC. CHEM. PATHOL. PHARMACOL.; U.S.A.; DA. 1974; VOL. 8; NO 3; PP. 527-534; BIBL. 1P.Article

Tetrahydroisoquinolines and β-carbolines: specific binding to human platelet α2-receptors in vitroGIVEN, M. B; LONGENECKER, G. L.Research communications in chemical pathology and pharmacology. 1983, Vol 41, Num 2, pp 349-352, issn 0034-5164Article

POLYMETHOXYLATED ISOQUINOLINES AS POTENTIAL ANTIMITOTIC AGENTS.IORIO M; BROSSIS A; CHIGNELL CE et al.1978; HETEROCYCLES; JAP.; DA. 1978; VOL. 9; NO 1; PP. 1-6; BIBL. 10 REF.Article

MASS SPECTRAL STUDIES OF AZA- AND DIAZABENZOBICYCLOALKANES. II. SOME ASPECTS OF MASS SPECTROMETRY OF 1,3-BRIDGED 1,2,3,4-TETRAHYDRONAPHTHALENES, 2,4-BRIDGED 1,2,3,4-TETRAHYDROISOQUINOLINES AND 1,3-BRIDGED 1,2,3,4-TETRAHYDROQUINOLINESSHIOTANI S; MITSUHASHI K.1972; CHEM. PHARM. BULL.; JAP.; DA. 1972; VOL. 20; NO 9; PP. 1980-1987; BIBL. 5 REF.Serial Issue

PHYSIKOCHEMISCHE EIGENSCHAFTEN UND MEMBRANWIRKUNG SPASMOLYTISCH WIRKSAMER ISOCHINOLIN-BZW. 1.2.3.4. TETRAHYDROISOCHINOLIN DERIVATE. = PROPRIETES PHYSICOCHIMIQUES ET ACTIVITE SUR LES MEMBRANES DES DENUES DE L'ISOQUINOLEINE OU DE LA TETRAHYDROISOQUINOLEINE AVEC UNE ACTIVITE SPASMOLYTIQUESIMON L; PORSZASZ J; GIBISZERKATALIN P et al.1977; PHARMAZIE; DTSCH.; DA. 1977; VOL. 32; NO 4; PP. 235-239; BIBL. 17 REF.Article

EFFECT OF HYDROGEN BONDING ON THE PI -ELECTRONIC ABSORPTION SPECTRA OF SOME BICYCLIC SECONDARY AMINESGANGULY T; BANERJEE SB.1982; CAN. J. CHEM.; ISSN 0008-4042; CAN; DA. 1982; VOL. 60; NO 6; PP. 741-746; ABS. FRE; BIBL. 19 REF.Article

KINETICS OF N-FORMYLATION OF 1,2,3,4-TETRAHYDROISOQUINOLINE WITH CHLORAL HYDRATEPEEREBOOM M; VAN DE LINDE A; MAAT L et al.1980; DELFT PROG. REP.; ISSN 501115; NLD; DA. 1980; VOL. 5; NO 2; PP. 126-130; BIBL. 13 REF.Article

ZUR REAKTIVITAET VON C=N-DOPPELBILDUNGSSYSTEMEN. XIV. UEBER DAS 3.4-DIHYDROISOCHINOLIN. = REACTIVITE DES DOUBLES LIAISONS C=N. XIV. DIHYDRO-3,4 ISOQUINOLEINEZIEGLER E; LEITNER W; STERK H et al.1978; Z. NATURFORSCH., B; DTSCH.; DA. 1978; VOL. 33; NO 6; PP. 640-645; ABS. ANGL.; BIBL. 9 REF.Article

POTENTIATION OF L-DOPA INDUCED MOTOR ACTIVITY BY AN INHIBITOR OF PHENYLETHANOLAMINE-N-METHYLTRANSFERASEKATZ RJ; GELBART J; CARROLL BJ et al.1980; PROGR. IN NEURO-PSYCHOPHARMACOL.; GBR; DA. 1980; VOL. 4; NO 1; PP. 101-105; BIBL. 17 REF.Article

CARBON-13 NUCLEAR MAGNETIC RESONANCE SPECTRA OF ISOQUINOLINE ALKALOIDS.SINGH SP; PARMAR SS; STENBERG VI et al.1978; J. HETEROCYCL. CHEM.; USA; DA. 1978; VOL. 15; NO 4; PP. 541-544; BIBL. 14 REF.Article

SYNTHESIS AND BIOLOGICAL ACTIVITY OF 2- AND 4-SUBSTITUTED 6,7-DIHYDROXY-1,2,3,4-TETRAHYDROISOQUINOLINESSMISSMAN EE; REID JR; WALSH DA et al.1976; J. MEDICIN. CHEM.; U.S.A.; DA. 1976; VOL. 19; NO 1; PP. 127-131; BIBL. 36 REF.Article

THE MASS SPECTRAL RETRO-DIELS-ALDER REACTION OF 1,2,3,4-TETRAHYDRONAPHTHALENE, ITS DERIVATIVES AND RELATED HETEROCYCLIC COMPOUNDSKUEHNE H; HESSE M.1982; MASS SPECTROMETRY REVIEWS; ISSN 513768; USA; DA. 1982; VOL. 1; NO 1; PP. 15-28; BIBL. 46 REF.Article

DRUG-INDUCED MODIFICATIONS OF THE IMMUNE RESPONSE. I. SUBSTITUTED 1-PHENYLISOQUINOLINESGEORGIEV VS; CARLSON RP; VAN INWEGEN RG et al.1979; J. MEDICIN. CHEM.; USA; DA. 1979; VOL. 22; NO 4; PP. 348-352; BIBL. 26 REF.Article

Selective inhibition of complex I of the brain electron transport system by tetrahydroisoquinolineSUZUKI, K; MIZUNO, Y; YOSHIDA, M et al.Biochemical and biophysical research communications (Print). 1989, Vol 162, Num 3, pp 1541-1545, issn 0006-291XArticle

Presence of tetrahydroisoquinoline and 1-methyl-tetrahydro-isoquinoline in foods: compounds related to Parkinson's diseaseMAKINO, Y; OHTA, S; TACHIKAWA, O et al.Life sciences (1973). 1988, Vol 43, Num 4, pp 373-378, issn 0024-3205Article

The preparation and oxidative dimerisation of 2-acetyl-7-hydroxy-1,2,3,4-tetrahydroisoquinoline. A new approach to tetrahydroisoquinoline synthesisAJAO, J. F; BIRD, C. W.Journal of heterocyclic chemistry. 1985, Vol 22, Num 2, pp 329-331, issn 0022-152XArticle

Enantioselective alkylation of α-amino carbanions. The synthesis of (S)-1-alkyl-1,2,3,4 tetrahydroisoquinolinesMEYERS, A. I; FUENTES, L. M; KUBOTA, Y et al.Tetrahedron (Oxford. Print). 1984, Vol 40, Num 8, pp 1361-1370, issn 0040-4020Article

A mechanistic model for asymmetric alkylation of chiral dipole stabilized anionsLOEWE, M. F; BOES, M; MEYERS, A. I et al.Tetrahedron letters. 1985, Vol 26, Num 28, pp 3295-3298, issn 0040-4039Article

Studies on the chemical constituents of rutaceous plants. LVI: The development of a versatile method for the synthesis of antitumor-active benzo[c]phenanthridine alkaloids. VI: Limitation of the Dyke synthetic pathway for benzo[c]phenanthridine alkaloidsISHII, H; ISHIDA, T.Chemical and pharmaceutical bulletin. 1984, Vol 32, Num 8, pp 3248-3251, issn 0009-2363Article

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