55540-33-5

Upstream product

• 5044-38-2 1-(4-chlorophenyl)-1H-pyrrole 
• 124-38-9 carbon dioxide 
• 106-47-8 4-chloro-aniline 
• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 7379-35-3 4-chlorpyridine hydrochloride 
• 89-77-0 2-Amino-4-chlorobenzoic acid 
• 635-21-2 5-chloroanthranilic acid 
• 5202-89-1 4-chlorobenzenesulfonyl chloride 

Downstream Products

• 133662-30-3 chlorure de 5-chloro-2-(1-pyrrolyl)benzoyle 
• 133662-35-8 5-chloro-2-(1-pyrrolyl)diazoacetophenone 
• 133662-39-2 acide 5-chloro-2-(1-pyrrolyl)phenyl acetique 

Relevant academic research and scientific papers

Br?nsted Acid-Catalyzed Asymmetric Ring-Closing Alkylation of Inert N-substituted Pyrroles with α, β-Unsaturated Ketones

A Chiral Br?nsted acid catalyzed asymmetric intramolecular ring-closing alkylation of inert pyrroles with α, β-unsaturated ketones has been developed. This approach gave a wide range of 4-phenyl-4,5-dihydro-6H-benzo[f]pyrrolo[1,2-a]azepin-6-ones in high yields with good enantioselectivities under mild reaction conditions. (Figure presented.).

Solvent and ligand effects on selective mono- and dilithiation of 1-(chlorophenyl)pyrroles and 1-(methoxyphenyl)pyrroles

Novel methods for site-selective lithiation of 1-(chlorophenyl)pyrroles and 1-(methoxyphenyl)pyrroles are described. Mono- or dilithiations are governed by change of both the temperature and the solvent from tetrahydrofuran to diethyl ether. Regioselectiv

Tricyclic oxime ethers

The present invention relates to compounds of formula (I): STR1 wherein A, x, y, R1, R2 and R3 are as defined in the description. The compounds are useful for treating diseases requiring a selective serotonin reuptake site

Oral hypoglycemic agents: 1(2 carboxyphenyl)pyrroles

A series of 1 (2 carboxyphenyl) pyrroles and their cyclized derivatives, pyrrolo [1,2 a]indoles, was synthesized and screened for hypoglycemic activity in rats. 1 (2 Carboxy 3 chlorophenyl) pyrrole was the most active, but had side effects.