65748-25-6

Upstream product

• 25939-01-9 p-toluoyl chloride phenylhydrazone 
• 70702-63-5 3-phenyl-4-p-tolyl-1,2,3-oxadiazol-3-ium-5-olate 
• 25939-01-9 4-methyl-N'-phenylbenzenecarbohydrazonoyl chloride 
• 20433-11-8 5-(4-methylphenyl)-2-phenyl-2H-tetrazole 

Downstream Products

• 104860-97-1 (3aS,4S,9bS)-4-Methyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104860-99-3 (3aS,4S,9bS)-4-Ethyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 129623-46-7 C₃₃H₃₀N₂O 
• 104861-04-3 (3aS,4S,5R,9bS)-4,5-Dimethyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104889-70-5 (3aS,4S,5R,9bS)-4-Ethyl-5-methyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104861-09-8 (3aS,4S,5R,9bS)-5-Ethyl-4-methyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104861-10-1 (3aS,4S,5R,9bS)-4,5-Diethyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104889-73-8 5-tert-Butyl-4-methyl-3-phenyl-1-p-tolyl-4,5-dihydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104861-14-5 (3aS,4S,5R,9bS)-4-Ethyl-5-isopropyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 104861-12-3 (3aR,4R,5S,9bR)-5-Isopropyl-4-methyl-3-phenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 110071-83-5 1,3,4-Triphenyl-6-p-tolyl-3b,4,6a,9b-tetrahydro-1H-9-thia-1,2,3a,4,5-pentaaza-trindene 
• 110071-85-7 3-(4-Methoxy-phenyl)-1,4-diphenyl-6-p-tolyl-3b,4,6a,9b-tetrahydro-1H-9-thia-1,2,3a,4,5-pentaaza-trindene 
• 123648-16-8 (3aR,9bR)-4-Methyl-3,5-diphenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 123648-17-9 (3aS,9bS)-4-Ethyl-3,5-diphenyl-1-p-tolyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 

Relevant academic research and scientific papers

Regioselective 1,3-dipolar cycloaddition of nitrilimines to 2-methyl-2-vinyl oxirane

1,3-Dipolar cycloaddition of in situ generated C,N-diaryl nitrilimines to 2-methyl-2-vinyl oxirane gives rise to the regioselective formation of novel 5-(2-methyloxiranyl)-4,5-dihydropyrazole derivatives in moderate to good yields. The structures and ster

Synthesis of 1,3,4-thiadiazolines from 1,2-dithiole-3-thiones

The thiocarbonyl group of 4,5-dichloro-1,2-dithiole-3-thione reacts as a 1,3-dipolarophile towards diaryl nitrile imines by 1,3-dipolar cycloaddition followed by opening of the dithiole ring with loss of sulfur to give 5-methylene-1,3,4-thiadiazolines; th

REACTION DE DIARYLNITRILIMINES SUR DES 2-ARYLIDENE-TETRALIN-1-ONES SUBSTITUEES. INFLUENCE DES FACTEURS CONFORMATIONNELS SUR LA DIASTEREOCHIMIE DE LA REACTION

Spiropyrazolines have been synthetized by 1,3-dipolar cycloaddition of some 2-arylidene-1-tetralones with diarylnitrilimines.It is shown that ring-closure reaction is regiospecific.The diastereoselectivity of the reaction is strongly dependent on the conf

The 1,3-dipolar cycloadditions of nitrile oxides and nitrile imines to alkyl dicyanoacetates

The readily available alkyl dicyanoacetates 1 reacted with the 1,3-dipolar reagents arenecarbonitrile oxides 2′ and arenecarbonitrile imines 5′ to afford 1,2,4-oxadiazol and 1,2,4-triazol derivatives. The arenecarbonitrile oxides 2′ with electron-donating

Photochemistry of Diarylsubstituted 2H-Tetrazoles, XI and Sydnones. V. Flashphotolytic Investigations with 2,5-Diaryl-2H-tetrazoles and 3,4-Diarylsydnones. Absolute Rate Constants of Cycloadditionreactions of Diarylnitrile Imines to Dipolarophils

The flash photolysis of 2,5-Diaryl-2H-tetrazoles 1 and 3,4-Diarylsydnones 2 was investigated.The nitrile imines were detected spectroscopically as short living intermediates.Rate constants of the cycloaddition reaction of nitrile imines and dipolarophiles

Photochemistry of Diarylsubstituted 2H-Tetrazoles. II. The Influence of the Substituents on the Absorption Properties of Diarylsubstituted Nitrilimines

Irradation of 2,5-diaryl-2H-tetrazoles in an EPA-glass (ether: i-pentan: ethanol = 5:5:2) or in an i-pentan glass at 77-80 K with UV-light of wavelength 290 nm yields diarylnitrilimines by the extrusion of nitrogen.The photoreactions investigated show spe