77219-99-9

Upstream product

• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 
• 32704-22-6 2-allyl-phenylamine 
• 63499-45-6 2-(2'-Allylanilino)-2-phenylessigsaeure-ethylester 

Downstream Products

• 77226-67-6 2-oxo-3a-methyl-1-phenyl-1,5-methano-1,2,4,5,6,11-hexahydro<1.3>oxazolo<3,2-a>quinoline 
• 77220-00-9 3-oxo-1-methyl-3a-phenyl-1,5-methano-1,3,4,5,6,11-hexahydro<1.3>oxazolo<3,4-a>-quinoline 
• 77226-67-6 C₁₉H₁₇NO₂ 
• 77220-00-9 1,4-methano-1H-oxazolo<3,4-a>quinolinone 
• 63499-46-7 2-(2'-Allyl-N-nitrosoanilino)-2-phenylessigsaeure 
• 98052-00-7 3a,4-dihydro-1-phenyl-3a-(trifluoromethyl)-1,4-methano-5H-oxazolo<3,2-a>quinolin-2(1H)-one 
• 63499-48-9 2-Phenyl-3a,4-dihydro-3H-pyrazolo<2,3-a>indol 
• 63499-44-5 3-(2'-Allylphenyl)-4-phenylsydnon 
• 77220-02-1 C₂₄H₁₉NO₂ 
• 77220-01-0 C₂₄H₁₉NO₂ 
• 77220-02-1 3a,4-dihydro-1,3a-diphenyl-1,4-methano-5H-oxazolo<3,2-a>quinoline-2(1H)-one 
• 77220-01-0 4,5-dihydro-1,3a-diphenyl-1,4-methano-1H-oxazolo<3,4-a>quinolin-3(3aH)-one 

Relevant academic research and scientific papers

Intramolecular 1,3-Dipolar Cycloaddition Reactions of Alkenyl-substituted 3,4-Diarylsydnones

The 3,4-diarylsydnones 1 and 12a-e with an allyl or alkenyloxy substituent on the N(3)-phenyl group have been synthesized by classical methods starting from 2-allylaniline and the corresponding alkenyloxyanilines, respectively (Schemes 2 and 3).Whereas th

Regiochemistry of Intramolecular Munchnone Cycloadditions: Preparative and Mechanistic Implications

A series of munchnone derivatives containing an internal ? bond were generated in situ by treating several N-(o-allylphenyl)alanines with acetic anhydride.The major product obtained corresponded to intramolecular 1,3-dipolar cycloaddition of the mesoionic