149597-98-8

Upstream product

• 149714-31-8 (R)-(-)-1-cyclohexyl-1-phenyl-2-propen-1-ol 
• 114531-88-3 (R)-(+)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid 
• 78620-93-6 (+/-)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid 
• 135033-55-5 (2R)-Benzoyl-3-oxa-1-azabicyclo<3.3.0>octane 
• 135033-59-9 (R)-Cyclohexyl-phenyl-(3R,7aS)-tetrahydro-pyrrolo[1,2-c]oxazol-3-yl-methanol 
• 20585-37-9 (R)-(-)-2-Cyclohexyl-2-hydroxy-2-phenyl-acetaldehyd 
• 10074-42-7 cyclohexyllithium 
• 1075-06-5 2,2-dihydroxy-1-phenyl-ethanone 
• 26482-37-1 (+/-)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid ethyl ester 
• 712-50-5 Cyclohexyl phenyl ketone 

Downstream Products

• 102473-43-8 Toluene-4-sulfonic acid (R)-3-cyclohexyl-3-hydroxy-3-phenyl-propyl ester 
• 149598-00-5 (R)-(-)-3-cyclohexyl-3-hydroxy-3-phenylpropyl 4-nitrobenzenesulfonate 
• 149714-31-8 (R)-(-)-1-cyclohexyl-1-phenyl-2-propen-1-ol 
• 149714-34-1 (2S,3R)-(-)-3-cyclohexyl-2,3-epoxy-3-phenyl-1-propanol 
• 149714-33-0 (+)-(2R,3R)-trans-3-cyclohexyl-3-phenyloxiranemethanol 
• 149598-02-7 (1R,2S)-(-)-1-cyclohexyl-2,3-epoxy-1-phenyl-1-propanol 
• 149598-03-8 (1R,2R)-(-)-1-cyclohexyl-2,3-epoxy-1-phenyl-1-propanol 
• 149714-36-3 (2S,3R)-(-)-3-cyclohexyl-2,3-epoxy-3-phenylpropyl 4-nitrobenzenesulfonate 
• 149714-37-4 (2R,3R)-(-)-3-cyclohexyl-2,3-epoxy-3-phenylpropyl 4-nitrobenzenesulfonate 
• 40520-25-0 (-)-Trihexyphenidyl 

Relevant academic research and scientific papers

Anticholinergic Agents 3. Synthesis and Configurational Assignment of the Four Stereoisomers of 1-Cyclohexyl-1,2-epoxy-1-phenyl-3-piperidinylpropane

The four stereoisomers of 1-cyclohexyl-1,2-epoxy-1-phenyl-3-piperidylpropane which are putative muscarinic antagonists, have been synthesised employing (S)- and (R)-1-cyclohexyl-1-phenyl-1,3-propanediol as chiral synthons.The relative configuration of the

Stereodivergent synthesis of optically active tertiary alcohols via addition reaction of chiral 2-acyl oxazolidine with organometallics

It was observed that diastereoselectivity in an addition reaction to chiral 2-acyl oxazolidine, derived from (S)-prolinol, can be fully regulated under appropriate conditions. Addition of organotitanium triisopropoxides provided (S)-tertiary alcohols, while organolithium reagents afforded the corresponding (R)-alcohols. Application of this methodology was demonstrated in the synthesis of (+)- and (-)-trihexyphenidyl.