877170-84-8

Upstream product

• 877170-77-9 tert-butyl 4-acetoxy-6,7-dihydro-1H-indole-1-carboxylate 
• 272456-69-6 (E)-methyl 2-diazo-4-(4-bromophenyl)but-3-enoate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 877170-76-8 4-oxo-4,5,6,7-tetrahydro-indole-1-carboxylic acid tert-butyl ester 

Downstream Products

• 877171-02-3 tert-butyl (S)-4-(1-(4-bromophenyl)-4-methoxy-4-oxobutyl)-1H-indole-1-carboxylate 

Relevant academic research and scientific papers

C-H activation as a strategic reaction: Enantioselective synthesis of 4-substituted indoles

A method is described for the asymmetric synthesis of 4-substituted indoles from the Rh2(S-DOSP)4-catalyzed decomposition of vinyldiazoacetates in the presence of N-Boc-4-acetoxy-6,7-dihydroindole. The reaction proceeds via a combine

4-Substituted and 7-substituted indoles, benzofurans, benzothiophenes, benzimidazoles, benzoxazoles, and benzothiazoles and methods for making same

Disclosed are 4-substituted and 7-substituted indoles, benzofurans, benzothiophenes, benzimidazoles, benzoxazoles, and benzothiazoles. Also disclosed are methods for making 4-substituted and 7-substituted indoles, benzofurans, benzothiophenes, benzimidazo