Synthesis, Functionalization, and Reactivity of Vinyl Sulfondiimidamides
Combining unsymmetrical sulfurdiimide reagents (R‐NSN‐R1) and Grignard reagents, followed by oxidative amination, delivers a series of vinyl sulfondiimidamides. Reactivity with cysteine and lysine derivatives is shown, and the cysteine reactivity is mapped in detail. Variation of the two imidic N‐substituents can be used to tune reactivity of these new
Katherine G. Rodden +4 more
wiley +2 more sources
The Pictet-Spengler Reaction Updates Its Habits
The Pictet-Spengler reaction (P-S) is one of the most direct, efficient, and variable synthetic method for the construction of privileged pharmacophores such as tetrahydro-isoquinolines (THIQs), tetrahydro-β-carbolines (THBCs), and polyheterocyclic ...
Andrea Calcaterra +9 more
doaj +1 more source
N-benzotriazol-1-yl-methyl-1,2,3,4-tetrahydroisoquinoline [PDF]
Benzotriazole-mediated heteroalkylations have been explored for many synthetic pathways.[...
Baldey, Sara +2 more
core +1 more source
Visible-light promoted atom transfer radical addition-elimination (ATRE) reaction for the synthesis of fluoroalkylated alkenes using DMA as electron-donor [PDF]
Here, we describe a mild, catalyst-free and operationally-simple strategy for the direct fluoroalkylation of olefins driven by the photochemical activity of an electron donor-acceptor (EDA) complex between DMA and fluoroalkyl iodides.
Gu, Jiwei +5 more
core +2 more sources
2-[(1R,3S)-6,7-Dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-3-yl]-4-phenyl-1,3-thiazole
In the title compound, C26H24N2O2S, the dihedral angle between the thiazole ring and the adjacent phenyl ring is 3.02 (15)°. The N-containing six-membered ring of the tetrahydroisoquinoline unit adopts a half-chair conformation.
Glenn E. M. Maguire +4 more
doaj +1 more source
Microwave-assisted synthesis of 1,2,3,4-tetrahydroisoquinoline sulfonamide derivatives and their biological evaluation [PDF]
Herein we report an alternative eco-friendly method for the synthesis of 1,2,3,4-tetrahydroisoquinoline sulfonamide derivatives. All obtained compounds were screened for their in vitro inhibition of albumin denaturation, antioxidant, antitryptic and ...
Manolov Stanimir P. +2 more
doaj +1 more source
Synthesis and Neurotropic Activity of Novel Quinoline Derivatives
Hydroxyalkyl and carboxyalkyl derivatives of silatetrahydroisoquinoline, tetrahydroisoquinoline and tetrahydroquinoline have been synthesized. Their neurotropic activity has been investigated.
Skaidrite Germane +3 more
doaj +1 more source
In the title molecule, C25H28N2O5S, (alternative name ethyl 2-{[7-acetyl-4-cyano-6-hydroxy-8-(4-methoxyphenyl)-1,6-dimethyl-5,6,7,8-tetrahydroisoquinolin-3-yl]sulfanyl}acetate) the 4-methoxyphenyl group is disposed on one side of the bicyclic core and ...
Elham A. Al-Taifi +6 more
doaj +1 more source
Structure–activity study of N-((trans)-4-(2-(7-cyano-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)cyclohexyl)-1H-indole-2-carboxamide (SB269652), a bitopic ligand that acts as a negative allosteric modulator of the dopamine D2 receptor [PDF]
We recently demonstrated that SB269652 (1) engages one protomer of a dopamine D2 receptor (D2R) dimer in a bitopic mode to allosterically inhibit the binding of dopamine at the other protomer.
Ananthan S. +61 more
core +2 more sources
4-[(2,4-Dimethyl-1,3-oxazol-5-yl)methyl]-4-hydroxy-2-methylisoquinoline-1,3(2H,4H)-dione
In the title isoquinolinedione derivative, C16H16N2O4, the piperidine ring in the tetrahydroisoquinoline unit adopts a half-boat conformation. The essentially planar oxazole ring [maximum deviation = 0.004 (2) Å] is inclined ...
Hoong-Kun Fun +3 more
doaj +1 more source

