Results 91 to 100 of about 4,486 (199)
Treatment with acetic anhydride-conc. sulufuric acid of o-quinol acetates (7, 11, 18, 19, 20, 28 and 34), which were derived from the corresponding 6-hydroxy-7-methoxytetrahydroisoquinolines (6, 12, 15, 16, 17, 27 and 31), gave the 5, 6-diacetates (8, 13, 21, 22, 23, 29 and 33, respectively). The diacetates were transformed into the corresponding 5, 6,
HIROSHI HARA +5 more
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Background The dopamine-derived tetrahydroisoquinolines (TIQ) synthesized endogeneously from aldehydes and catecholamines have shown to modulate neurotransmission, central metabolism and motor activity. Converging evidence has implicated abnormalities of
Rothenberger Aribert +6 more
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Mechanochemistry has emerged as a potential alternative for organic transformations, leveraging substrate availability, stability, and reduced solvent use.
Stanimir Manolov +3 more
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Tetrahydroisoquinolines (THIQs) are a significant class of nitrogen-containing heterocyclic compounds often occurring in natural products and pharmaceuticals, exhibiting excellent biological activities and chemical properties, and also having a wide ...
Kai Yang +5 more
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Chiral N-acyliminium ions as new tools in the asymmetric synthesis of CNS-active compounds [PDF]
Beutler +9 more
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Enantiopure 3-methyl-3,4-dihydroisocoumarins and 3-methyl-1,2,3,4-tetrahydroisoquinolines via chemoenzymatic asymmetric transformations [PDF]
Busto García, Benjamín Eduardo +3 more
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Dicentrine: The Major Alkaloid of Cyclea laxiflara Miers [PDF]
The major alkaloid of Cyclea laxiflora Miers.
Ismail, Norhayati +2 more
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In this study, new tetrahydroisoquinoline compounds were synthesized by reaction of 7-Acetyl-4-cyano-1,6-dimethyl-6-hydroxy-8- (3-nitrophenyl or 4-nitrophenyl)-5,6,7,8-tetrahydrosoquinoline-3(2H)-thiones with methyl iodide, chloro acetonitrile, ethyl ...
Etify A. Bakhite +4 more
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Enantioselective palladium(0)-catalyzed C-H arylation strategy for chiral heterocycles [PDF]
Transition-metal-catalyzed C-H functionalizations have emerged as complementary and powerful tools to access molecular complexity from widely available starting materials.
Cramer, Nicolai, Saget, Tanguy
core
HARMACOLOGY OF 1,2,3,4-TETRAHYDROISOQUINOLINES
Tursunkhodzhaeva F.M, Azamatov A.A.
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