Results 61 to 70 of about 5,203 (175)

(S)-Methyl 2-[(3R,4R)-2-benzyl-3-(2-furyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamido]-3-(1H-indol-3-yl)propanoate

open access: yesActa Crystallographica Section E, 2009
The title compound, C33H29N3O5, was synthesized by the reaction of racemic trans-2-benzyl-3-(2-furyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid, l-tryptophan methyl ester and diisopropylcarbodiimide in dry dichloromethane.
Zeliha Baktır   +4 more
doaj   +1 more source

Studies on tetrahydroisoquinolines. XX. A novel synthesis of 8-aryl-1,2,3,4-tetrahydroisoquinolines.

open access: yesChemical and Pharmaceutical Bulletin, 1983
Treatment of a mixture of the p-quinol acetate (4) and aryl ethers with trifluoroacetic acid gave 8-aryl-1, 2, 3, 4-tetrahydroisoquinolines (1a-f) in good yields. Similar reaction of 4 and corypalline (3) afforded a corypalline dimer (5).
HARA, HIROSHI   +2 more
openaire   +2 more sources

Acid Catalyzed Formation of C–C and C–S Bonds via Excited State Proton Transfer

open access: yesMolecules, 2019
The behavior of 2-naphthol and 7-bromo-2-naphthol as organic photoacids are exploited in organic synthesis for the preparation of benzyl sulfides (using a trichloroacetimidate derivative as the starting substrate) and polycyclic amines via acid catalyzed
Alessandro Strada   +3 more
doaj   +1 more source

1,2,3,4-Tetrahydroisoquinoline-2-sulfonamide

open access: yesActa Crystallographica Section E, 2008
The title compound, C9H12N2O2S, is a useful precursor of a variety of modified sulfonamide molecules. Due to the importance of these molecules in biological systems (antibacterials, antidepressants and many other applications), there is a growing ...
Carole Barbey   +3 more
doaj   +1 more source

One-pot Ugi-azide and Heck reactions for the synthesis of heterocyclic systems containing tetrazole and 1,2,3,4-tetrahydroisoquinoline

open access: yesBeilstein Journal of Organic Chemistry
A new method for the synthesis of heterocyclic systems containing tetrazole and tetrahydroisoquinoline is developed via the performance of one-pot Ugi-azide and Heck cyclization reactions.
Jiawei Niu   +6 more
doaj   +1 more source

Asymmetric Synthesis of Tetrahydroisoquinoline Alkaloids Using Ellman's Chiral Auxiliary

open access: yesNatural Product Communications, 2017
Chiral t -butylsulfinamide has been successfully employed for the stereoselective synthesis of 1-benzyl tetrahydroisoquinoline alkaloids. This is the first report on the synthesis of chiral 1-benzyltetrahydroisoquinoline natural products using tert ...
Y. Vikram Reddy   +5 more
doaj   +1 more source

Synthesis of Some Novel 11b-Substituted Pyrimido[6,1-a]-isoquinoline Derivatives

open access: yesMolecules, 2004
A series of novel 11b-substituted 1,6,7,11b-tetrahydropyrimido[6,1-a]- isoquinoline-2,4-diones and 4-thioxo-1,3,4,6,7,11b-hexahydropyrimido[6,1-a]isoquinolin-2- ones were synthesized, utilizing two alternative strategies for ring closure of ...
Atanas P. Venkov   +2 more
doaj   +1 more source

(S)-4-tert-Butyl-2-(1,2,3,4-tetrahydroisoquinolin-3-yl)-1,3-thiazole

open access: yesActa Crystallographica Section E, 2012
In the title compound, C16H20N2S, a potential tetrahydroisoquinoline (TIQ) thiazole ligand, the N-containing six-membered ring of the TIQ unit adopts a half-chair conformation. There are four molecules in the asymmetric unit.
Sunayna Pawar   +3 more
doaj   +1 more source

Heterogeneous Catalysts in Pictet-Spengler-Type Reactions

open access: yesJournal of Chemistry, 2013
Several solid catalysts were evaluated as an alternative for 1,2,3,4-tetrahydroisoquinoline synthesis by means of the Pictet-Spengler reaction. The reaction catalysed by a mixed oxide (Mg and Al) led to the best yield and good regioselectivity; using an ...
Rodolfo Quevedo   +2 more
doaj   +1 more source

2-Phenylquinolines Exhibit Anti-Severe Acute Respiratory Syndrome Coronavirus-2 Activity Through the Nonstructural Protein 13 Helicase Inhibition. [PDF]

open access: yesChemMedChem
Cernicchi G   +24 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy