1312002-41-7

Upstream product

• 91107-10-7 4,6-dimethoxy-2,3-diphenyl-1H-indole 
• 76-02-8 trifluoroacetyl chloride 

Downstream Products

• 1312002-50-8 allyl 1-allyl-4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carboxylate 
• 1312002-67-7 (1-allyl-4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)(2H-pyrrol-1-yl)methanone 
• 1312002-66-6 C₃₂H₃₂N₂O₃ 
• 1312002-43-9 allyl 4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carboxylate 
• 1312002-65-5 N-allyl-4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carboxamide 
• 1569643-08-8 5,5'-bis(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-2,2'-bi-(1,3,4-oxadiazole) 
• 1569642-86-9 N,N′-bis(4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carbonyl)oxalohydrazide 
• 1569642-67-6 4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carbohydrazide 
• 1569642-50-7 2,5-di(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-1,3,4-oxadiazole 
• 1569642-33-6 N,N'-bis(4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carbonyl) hydrazide 
• 1422975-95-8 N-(2-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-2-oxoethyl)-4,6-dimethoxy-2,3-diphenyl-1H-indole-7-carboxamide 

Relevant academic research and scientific papers

Synthesis and biological evaluation of 2,5-di(7-indolyl)-1,3,4-oxadiazoles, and 2- and 7-indolyl 2-(1,3,4-thiadiazolyl)ketones as antimicrobials

A range of novel hydrazine bridged bis-indoles was prepared from readily available indole-7-glyoxyloylchlorides and 7-trichloroacetylindoles and underwent cyclodehydration to produce 2,5-di(7-indolyl)-1,3,4-oxadiazoles and a 2,2′-bi-1,3,4-oxadiazolyl with

Ring closing metathesis strategies towards functionalised 1,7-annulated 4,6-dimethoxyindoles

A ring closing metathesis approach has been used to prepare a novel range of indoles 1,7-annulated with nitromethyl and lactone functionalised medium-sized rings. Initial studies into the preparation of lactam functionalised rings are also discussed.