63499-48-9

Upstream product

• 130420-55-2 (2SR,3aSR)-2-hydroxymethyl-2-phenyl-2,3,3a,4-tetrahydro-1H-pyrazolo<1.5-a>indole 
• 130420-65-4 (2SR,3aSR)-2-phenyl-2,3,3a,4-tetrahydro-1H-pyrazolo<1.5-a>indole 
• 130420-72-3 (2SR,3aSR)-2-carbomethoxy-2-phenyl-2,3,3a,4-tetrahydro-1H-pyrazolo<1.5-a>indole 
• 130420-61-0 methyl benzoylformate (Z)-2-allylphenylhydrazone 
• 130420-64-3 methyl benzoylformate (E)-2-allylphenylhydrazone 
• 130420-48-3 N-(2-allylphenyl)hydrazine 
• 130420-73-4 2-carboxymethyl-2-phenyl-2,3-dihydro-1H-pyrazolo<1.5-a>indole 
• 63499-46-7 2-(2'-Allyl-N-nitrosoanilino)-2-phenylessigsaeure 
• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 
• 77219-99-9 2-(2'-Allylanilino)-2-phenylessigsaeure 
• 63499-45-6 2-(2'-Allylanilino)-2-phenylessigsaeure-ethylester 
• 32704-22-6 2-allyl-phenylamine 
• 157403-17-3 tert-butyl 2-phenyl-3a,4-dihydro-1H-pyrazolo<1,5-a>indole-1-carboxylate 
• 63499-44-5 3-(2'-Allylphenyl)-4-phenylsydnon 

Relevant academic research and scientific papers

Preparation and Reaction of 1H-Pyrazoloindoles as Isoelectronic Analogues of Azulene (Pseudoazulene)

We have prepared 1H-pyrazoloindoles for the first time and have found that they have the chemical behaviour of isoelectronic analogues of azulene (pseudoazulene).

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