100199-10-8

Upstream product

• 288-32-4 1H-imidazole 
• 1056477-06-5 2-bromocyclohexanone 
• 286-20-4 cyclohexene oxide 
• 129500-93-2 2-(imidazol-1-yl)cyclohexanol 

Downstream Products

• 100199-22-2 (1S,2S)-1-(3,4-Dichloro-phenyl)-2-imidazol-1-yl-cyclohexanol 
• 100199-22-2 (1S,2R)-1-(3,4-Dichloro-phenyl)-2-imidazol-1-yl-cyclohexanol 
• 100199-32-4 (1S,2S)-1-(4-Fluoro-phenyl)-2-imidazol-1-yl-cyclohexanol 
• 100199-32-4 (1S,2R)-1-(4-Fluoro-phenyl)-2-imidazol-1-yl-cyclohexanol 
• 100199-29-9 (1S,2S)-1-(4-Chloro-phenyl)-2-imidazol-1-yl-cyclohexanol 
• 100199-29-9 (1S,2R)-1-(4-Chloro-phenyl)-2-imidazol-1-yl-cyclohexanol 

Relevant academic research and scientific papers

Kinetic Resolution Driven Diastereo- and Enantioselective Synthesis of cis-β-Heteroaryl Amino Cycloalkanols by Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation

The utility of tethered Ru-TsDPEN catalyst has been demonstrated for the asymmetric transfer hydrogenation of rac-α-heteroaryl amino cycloalkanones to construct biologically important cis-β-heteroaryl amino cycloalkanols with two contiguous chiral centers

Azolyl cycloalkanol derivatives and agricultural fungicides

Novel 1-substituted -2-imidazolyl (or 1,2,3-triazolyl)cyclohexanols or cycloheptanols having anti-fungal activity against wide range of agricultural fungi with vapor effect.

SYNTHESIS OF 2-AZOLYLCYCLOALKANOLS

New 2-azolylcycloalkanol derivatives (13-38) were synthesized stereoselectively by Grignard reaction of 2-azolylcyclohexanones (7,8), and particularly 2-azolylcycloheptanones (9,10) afforded one of the diastereomers of 2-azolylcycloalkanols stereospecific