1361316-77-9

Upstream product

• 603-35-0 triphenylphosphine 
• 26087-01-4 (Z)-2-azido-1,3-diphenylprop-2-en-1-one 
• 26086-60-2 2-azido-4'-chloroacetophenone 
• 100-52-7 benzaldehyde 
• 26087-01-4 2-azido-1,3-diphenylpropen-1-one 
• 1816-88-2 2-azido-1-phenylethan-1-one 

Downstream Products

• 1360554-91-1 2-benzyl-3-phenyl-1,2,4-triazino[2,3-b]indazole 
• 1360555-01-6 3-benzylidene-2-phenyl-3H-1,4-benzodiazepine 
• 1360554-81-9 2-(azidobenzylideneamino)-1,3-diphenylprop-2-en-1-one 
• 1361316-74-6 (2-methyl-5-phenyloxazol-4-yl)(phenyl)methanol 
• 1361316-76-8 (phenyl)(5-phenyl-2-propyloxazol-4-yl)methanol 
• 1361316-62-2 [2-(4-fluorophenyl)-5-phenyloxazol-4-yl](phenyl)methanol 
• 1361316-66-6 [2-(3-chlorophenyl)-5-phenyloxazol-4-yl](phenyl)methanol 
• 1361316-64-4 [2-(2-chlorophenyl)-5-phenyloxazol-4-yl](phenyl)methanol 
• 24806-70-0 N-[(Z)-1-oxo-1,3-diphenylprop-2-en-2-yl]benzamide 
• 133229-66-0 (2,5-diphenyloxazol-4-yl)(phenyl)methanol 
• 1361316-63-3 [2-(4-methylphenyl)-5-phenyloxazol-4-yl](phenyl)methanol 
• 1361316-61-1 [2-(4-chlorophenyl)-5-phenyloxazol-4-yl](phenyl)methanol 

Relevant academic research and scientific papers

Unexpected synthesis of 2,4,5-trisubstituted oxazoles via a tandem aza-wittig/michael/isomerization reaction of vinyliminophosphorane

2,4,5-Trisubstituted oxazoles 6 were unexpectedly prepared from a tandem reaction of vinyliminophosphorane 3 with various acyl chlorides in a one-pot fashion.

Temperature-dependent regioselective synthesis of 1,2,4-triazino[2,3-b] indazoles and 3H-1,4-benzodiazepines by domino-Staudinger/aza-Wittig/ isomerization reaction

o-Azidobenzaldimine 8 reacted with triphenylphosphane at 0 °C with warming to room temperature to give 1,2,4-triazino[2,3-b]indazoles 12 by a domino-Staudinger/aza-Wittig/isomerization reaction. However, when heated to 80 °C the same reaction mixture affo