Results 181 to 190 of about 34,528 (221)
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Allylboration of Functionalized Isoquinolines.
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Fedor V. Pastukhov +3 more
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Enantioselective Hydrogenation of Isoquinolines
Angewandte Chemie International Edition, 2013AbstractReview: [11 refs.]
Dongbing Zhao, Frank Glorius
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1971
1. ISOQUINOLINE ALKALOIDS - ORIGINS AND DEGREDATION 2. ss-PHENYLETHYLAMINES AND SIMPLE ISOQUINOLINES 2.1 Structures 2.2 Syntheses 2.3 Chemical Properties 2.4 Polymeric Isoquinolines 2.5 N-Benzylisoquinolines 2.6 1-Phenylisoquinolines 2.7 4-Phenylisoquinolines 2.8 Biogenesis 2.9 Pharmacology References 3.
J. E. Saxton, K. W. Bentley
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1. ISOQUINOLINE ALKALOIDS - ORIGINS AND DEGREDATION 2. ss-PHENYLETHYLAMINES AND SIMPLE ISOQUINOLINES 2.1 Structures 2.2 Syntheses 2.3 Chemical Properties 2.4 Polymeric Isoquinolines 2.5 N-Benzylisoquinolines 2.6 1-Phenylisoquinolines 2.7 4-Phenylisoquinolines 2.8 Biogenesis 2.9 Pharmacology References 3.
J. E. Saxton, K. W. Bentley
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ChemInform Abstract: CONDENSED ISOQUINOLINES. XI. IMIDAZO(5,1‐A)ISOQUINOLINES
Chemischer Informationsdienst, 1976AbstractDas aus (I) zugängliche Carbonitril (II) wird katalytisch zu dem Amin (III) hydriert, dessen Acetylierung die Produkte (IV), (Va), (Vb) sowie das bekannte Imidazoisochinolin (Xd) gibt; demnach unterliegt (Vb) unter den vorhandenen Bedingungen bereits der Cyclokondensation zu (Xd).
Willy R. F. Lingier +3 more
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1978
The chemistry, synthesis, and biogenesis of peyote, Lophophora williamsii (Lemaire) Coult., and other cactus alkaloids have been thoroughly reviewed.1 ...
Maurice Shamma, Jerome L. Moniot
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The chemistry, synthesis, and biogenesis of peyote, Lophophora williamsii (Lemaire) Coult., and other cactus alkaloids have been thoroughly reviewed.1 ...
Maurice Shamma, Jerome L. Moniot
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3,4-Dihydrobenz[f]isoquinoline and 3,4-dihydrobenz[g]isoquinoline
The Journal of Organic Chemistry, 1988AbstractThe isoquinolines (II) and (IX) mentioned in the title are prepared by cyclization of the N‐naphthylethyl formamide (I) or by cyclocondensation of the diacid monoester (V) with urea (VI) and subsequent reduction and dehydrogenation.
Steven D. Young +2 more
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1988
Publisher Summary Isoquinoline-type alkaloids show biological activities similar to those of morphinane-, protoberberine-, and benzophenanthridine-type alkaloids. The benzophenanthridine alkaloids found in callus cells of poppy are not present in the original plants.
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Publisher Summary Isoquinoline-type alkaloids show biological activities similar to those of morphinane-, protoberberine-, and benzophenanthridine-type alkaloids. The benzophenanthridine alkaloids found in callus cells of poppy are not present in the original plants.
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Asymmetric Synthesis of Isoquinoline Alkaloids
Chemical Reviews, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
Maria Chrzanowska, Maria D. Rozwadowska
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Cyanochlorination and cyanogenation of isoquinoline
Journal of the Chemical Society D: Chemical Communications, 1969Isoquinoline reacts with potassium cyanide and sulphuryl chloride to give, depending upon the reaction conditions, 4-chloro-1-cyano-, 1,3-dicyano-, 1-aminocarbonyl-3-cyano-, 3-cyano-, and 1-cyano-isoquinoline, thus illustrating a simple method for the direct introduction of chloro- and cyano-substituents into nitrogen heterocycles.
S. L. Tan, B. C. Uff, G. W. Kirby
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Isoquinolines as receptors for resorcinol
Tetrahedron Letters, 1994Abstract Multiple condensation reactions based on the Pictet-Gams isoquinoline synthesis lead to receptors for resorcinol. The host-guest interaction is confirmed by anisotropic highfield shifts and by NOE enhancement between aryl protons.
Gerald Dyker +3 more
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