937059-69-3

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 873-38-1 4-chloro-2-bromoaniline 

Downstream Products

• 937058-82-7 ethyl (E)-[1-[3-[1-[4-chloro-2-[1-(2-ethoxy-3-methoxyphenyl)-1-hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acryloxy]piperidin-4-yl]acetate 
• 937058-91-8 ethyl (E)-[1-[3-[1-[4-chloro-2-[1-(3-methoxyphenyl)-1-hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acryloxy]piperidin-4-yl]acetate 
• 937056-44-5 Ethyl 2-[1-[2-[8-chloro-6-(2-ethoxy-3-methoxyphenyl)-4H,6H-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl]acetyl]4-piperidinyl]acetate 
• 937056-45-6 2-[1-[2-[8-Chloro-6-(2-ethoxy-3-methoxyphenyl)-4H,6H-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl]acetyl]4-piperidinyl]acetic acid 
• 937056-46-7 Ethyl 2-[1-[2-[8-chloro-6-(3-methoxyphenyl)-4H,6H-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl]acetyl]4-piperidinyl]acetate 
• 937056-47-8 2-[1-[2-[8-Chloro-6-(3-methoxyphenyl)-4H,6H-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl]acetyl]4-piperidinyl]acetic acid 
• 937058-80-5 3-[1-[4-Chloro-2-[(2-ethoxy-3-methoxyphenyl)hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acrylic acid 
• 937058-78-1 methyl (E)-3-[1-[4-chloro-2-[(2-ethoxy-3-methoxyphenyl)hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acrylate 
• 937058-76-9 methyl (E)-3-[1-[4-chloro-2-(2-ethoxy-3-methoxybenzoyl)phenyl]-1H-pyrrol-2-yl]acrylate 
• 937058-90-7 3-[1-[4-Chloro-2-[(3-methoxyphenyl)hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acrylic acid 
• 937058-89-4 Methyl 3-[1-[4-chloro-2-[(3-methoxyphenyl)hydroxymethyl]phenyl]-1H-pyrrol-2-yl]acrylate 
• 937058-88-3 methyl (E)-3-[1-[4-chloro-2-(3-methoxybenzoyl)phenyl]-1H-pyrrol-2-yl]acrylate 
• 937058-72-5 1-[4-Chloro-2-(2-ethoxy-3-methoxybenzoyl)phenyl]-1H-pyrrol-2-carbaldehyde 
• 937058-74-7 1-[4-chloro-2-(2-ethoxy-3-methoxybenzoyl)phenyl]-1H-pyrrol-3-carbaldehyde 

Relevant academic research and scientific papers

C-H bond functionalization in the synthesis of fused 1,2,3-triazoles

A highly modular approach to fused 1,2,3-triazoles has been developed featuring a one-pot procedure combining copper(I) catalyzed azide-alkyne cycloaddition and palladium-catalyzed C-H bond functionalization. A class of structurally unique heterocycles was synthesized in good yields.

Palladium-catalyzed annulation of aryl heterocycles with strained alkenes

An annulation reaction proceeding by the intermolecular addition of an arylpalladium(II) halide across a strained alkene, followed by an intramolecular C-H functionalization of a pendant heterocycle is described. A variety of polycyclic heterocycles have