55077-51-5

Upstream product

• 55578-83-1 2-(2-azidophenyl)furan 
• 3302-39-4 1-azido-2-bromobenzene 
• 615-36-1 2-bromoaniline 
• 55578-79-5 2-(2-aminophenyl)furan 

Downstream Products

• 66424-75-7 4-benzoyl-4H-furo[3,2-b]indole 
• 65172-82-9 4-(4-ethyl-4H-furo[3,2-b]indol-2-ylmethyleneamino)-1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one 
• 61341-53-5 4-(4-ethyl-4H-furo[3,2-b]indol-2-ylmethyleneamino)-benzoic acid ethyl ester 
• 61082-88-0 2-(4-nitro-styryl)-4H-furo[3,2-b]indole 
• 61082-85-7 2-styryl-4H-furo[3,2-b]indole 
• 66424-77-9 2,4-dibenzoyl-4H-furo[3,2-b]indole 
• 66424-78-0 2-acetyl-4-benzoyl-4H-furo[3,2-b]indole 
• 66424-76-8 4-benzoyl-2-bromo-4H-furo[3,2-b]indole 
• 61082-86-8 4-[2-(4H-furo[3,2-b]indol-2-yl)-vinyl]-benzonitrile 
• 55578-78-4 (4H-furo[3,2-b]indol-2-yl)-phenyl-methanone 

Relevant academic research and scientific papers

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

Disclosed are a fused compound having excellent emission wavelength control and luminous efficiency, a method for manufacturing the same, and an organic electronic device including the fused compound. Symmetric, asymmetric, and planar structures of the pr

Compound taking quinolinone derivative as core and application of compound in organic electroluminescent device

The invention discloses a compound taking a quinolinone derivative as a core and an application of the compound in an organic electroluminescent device. The compound structurally contains the quinolinone derivative as an electron acceptor, so that transmi

Gold-Catalyzed Cascade Reactions of 4 H-Furo[3,2-b]indoles with Allenamides: Synthesis of Indolin-3-one Derivatives

Merging the ability of cationic gold(I) catalysts to activate unsaturated π-systems with the electrophiles-driven ring-opening reactions of furans, we describe a new approach to synthesize 2-spiroindolin-3-ones from 4H-furo[3,2-b]indoles. The reaction occ

First Suzuki-Miyaura type cross-coupling of ortho-azidobromobenzene with arylboronic acids and its application to the synthesis of fused aromatic indole-heterocycles

A short synthesis of some fused indole-heterocycles has been achieved via Pd-catalyzed cross-coupling reactions between azido-2-bromobenzene and arylboronic acids and subsequent thermally induced nitrene insertion. Additionally, 4-amino-α-carboline, a versatile intermediate toward grossularine analogs has also been prepared by Suzuki-Miyaura cross-coupling of 4-pivaloylaminopyridine-3-boronic acid with 2-bromoaniline, followed by simple functional group transformations.