82672-31-9

Upstream product

• 82672-21-7 C₃₂H₂₆N₄S₂ 
• 75-11-6 diiodomethane 
• 1826-17-1 4-methyl-2-phenyl-thiazole 
• 82672-17-1 4-methyl-2-phenylthiazole 3-oxide 
• 14465-74-8 N-phenyl-N-prop-2-ynylamine 
• 100-47-0 benzonitrile 
• 62-53-3 aniline 
• 40366-99-2 N-allyl-N-phenyl-phenylamidine 
• 142-71-2 copper diacetate 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 589-09-3 N-allyl-N-phenylamine 
• 350-46-9 4-Fluoronitrobenzene 
• 827-43-0 4-methyl-2-phenyl-1H-imidazole 
• 850338-83-9 4-methyl-1-(4-nitrophenyl)-2-phenyl-1H-imidazole 

Relevant academic research and scientific papers

Ln[N(SiMe3)2]3-Catalyzed Cross-Diinsertion of C≡N/C≡C into an N-H Bond: Facile Synthesis of 1,2,4-Trisubstituted Imidazoles from Propargylamines and Nitriles

A lanthanide-catalyzed sequential insertion of C≡N and C≡C into an N-H bond is presented. The convenient reaction, which proceeds under mild conditions, is an efficient method for preparing 1,2,4-trisubstituted imidazoles directly from readily available propargylamines and nitriles.

Unusual 1,4-methylene transfer from a Simmons-Smith reagent to 1,3- diazabuta-1,3-dienes

Novel 1,4 methylene transfer from a Simmons-Smith reagent to 1-aryl-4- secondary amino-4-methylthio or methyl-2-phenyl-1,3-diazabuta-1,3-dienes leading to 1-aryl-2-phenyl-4-secondary amino or methyl-imidazoles are described.

Cu(II)-mediated aminooxygenation of alkenylimines and alkenylamidines with TEMPO

A method for the synthesis of oxymethyl dihydropyrroles (pyrrolines) and dihydroimidazoles has been developed via Cu(II)-mediated intramolecular aminooxygenation of alkenylimines and alkenylamidines, respectively, with 2,2,6,6-tetramethyl-1-piperidinyloxy radical (TEMPO). Georg Thieme Verlag Stuttgart · New York.

Synthesis, structure-activity relationships at the GABAA receptor in rat brain, and differential electrophysiological profile at the recombinant human GABAA receptor of a series of substituted 1,2-diphenylimidazoles

A series of new 1,2-diphenylimidazole derivatives (1a-x) were synthesized and evaluated for their ability to potentiate γ-aminobutyric acid (GABA)-evoked currents in Xenopus laevis oocytes expressing recombinant human GABAA receptors. Many of t

Studies on Azole Compounds. VI. Reactions of 2,4- and 2,5-Disubstituted Thiazole N-Oxides with Aryl Isocyanates

The reactions of 2,4- (Ia-d) and 2,5-disubstituted thiazole 3-oxides (Ie-f) with aryl isocyanates (II) were studied.While the reactions of Ia-d with II proceeded smoothly to give bis(5-imidazolyl) disulfides (IV), those of Ie-f with II did not take place.