1220532-29-5

Upstream product

• 1220532-28-4 4-[(3-phenyl)-3-hydroxyprop-1-yl]-1-trityl-1H-imidazole 
• 100-58-3 phenylmagnesium bromide 
• 102676-61-9 3-(1-triphenylmethyl-4-imidazolyl)propionaldehyde 
• 1334230-64-6 4-[(3-phenyl)-3-chloroprop-1-yl]-1-trityl-1H-imidazole 

Downstream Products

• 1220532-30-8 (R)-5-phenyl-6,7-dihydro-5H-pyrrolo-[1,2-c]imidazole 
• 1220532-31-9 (S)-5-phenyl-6,7-dihydro-5H-pyrrolo-[1,2-c]imidazole 
• 1220532-38-6 (R)-2-isopropyl-5-phenyl-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-2-ium bromide 
• 1220532-39-7 (R)-5-phenyl-2-(2-pyridinylmethyl)-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-2-ium bromide 

Relevant academic research and scientific papers

IMIDAZOLIUM SALT AND ASYMMETRIC SYNTHESIS CATALYST PREPARED THEREWITH, AND METHOD FOR PRODUCING IMIDAZOLIUM SALT

PROBLEM TO BE SOLVED: To provide a variety of optically active imidazolium salts produced efficiently and conveniently. SOLUTION: The present invention provides an imidazolium salt represented by general formula (1). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

IMIDAZOLIUM SALT, ASYMMETRIC SYNTHESIS CATALYST USING THE SAME, AND METHOD FOR PRODUCING IMIDAZOLIUM SALT

PROBLEM TO BE SOLVED: To provide a novel optically active imidazolium salt for the synthesis of nitrogen-containing heterocyclic carbene as the ligand of organic catalyst and metal catalyst, in particular a bicyclic optically active imidazolium salt, and a method of producing the same. SOLUTION: The present invention provides an imidazolium salt represented by formula (1). (R1-R5 are H, hydrocarbon groups each independently or adjacently forming a ring, alkoxy groups, aryloxy groups, alkylthio groups, arylsulfonyl groups, or the like; X is a substituted/unsubstituted C1-C4 carbon chain, a substituted/unsubstituted N, O, S, or an atom group comprising a combination of Cs optionally substituted with these hetero atoms; Z is a halogen atom, PF6, BF4, ClO4, or BPh4). COPYRIGHT: (C)2015,JPOandINPIT

Bicyclic imidazoles for modular synthesis of chiral imidazolium salts

The preparation of new chiral bicyclic imidazoles 5 and their transformation into imidazolium salts 6 and 7 are reported. The utility of the salts as precursors for chiral N-heterocyclic carbenes was demonstrated by the synthesis of C-N-C pincer Ni-complex 13h, the structure of which was characterized by single-crystal X-ray analysis.