885722-03-2

Upstream product

• 87963-20-0 1,3-diethyl-benzoimidazolium 
• 103-72-0 phenyl isothiocyanate 
• 95348-62-2 1,3-diethyl-1H-benzo[d]imidazol-3-ium bromide 

Downstream Products

• 885722-29-2 ethyl 1,3-diethyl-1'-phenyl-2',3'-dihydrospiro[benzimidazoline-2,3'-pyrrole]-2'-thione-4'-carboxylate 
• 885722-13-4 dimethyl 1,3-diethyl-2'-phenylimino-2',3'-dihydrospiro[benzimidazoline-2,3'-thiophene]-4',5'-dicarboxylate 
• 1123535-03-4 (Z,Z)-methyl 2-[4'-benzyl-1,3-diethyl-1,3,4',5'-tetrahydro-2'-(phenylimino)spiro[benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate 

Relevant academic research and scientific papers

An experimental and theoretical study on the interaction of N-heterocyclic carbene-derived 1,3-dipoles with methoxycarbonylallenes: Highly regio- and stereoselective [3+2]-cycloadditions controlled by the structures of N-heterocycles of 1,3-dipoles

The reactions of N-heterocyclic carbene-derived 1,3-dipoles with methoxycarbonylallenes were studied systematically by means of experimental and theoretical approach. The regioselectivity of [3+2]-cycloaddition of 1,3-dipoles toward the ester-substituted

A N-heterocyclic carbene derived highly regioselective ambident C-C-S and C-C-N 1,3-dipolar system

N-Heterocyclic carbene derived 2-phenylthiocarbamoyl benzimidazolium and imidazolinium inner salts are a unique ambident C-C-S and C-C-N 1,3-dipolar system able to undergo highly efficient and regioselective cycloaddition with dimethyl acetylenedicarboxyl