526221-22-7

Upstream product

• 67-66-3 chloroform 
• 98857-41-1 (R)-(+)-1-trimethylsiloxyethylbenzene 
• 1517-69-7 (R)-1-phenylethanol 

Downstream Products

• 682351-17-3 (R)-2-hydroxy-2-phenylpropanal dimethyl acetal 
• 526221-29-4 (S)-3-Hydroxy-2-methyl-2-phenyl-succinonitrile 
• 526221-30-7 (S)-3-Hydroxy-2-methyl-2-phenyl-propionitrile 
• 526221-27-2 (R)-2-Azido-2-phenyl-propionaldehyde 
• 29738-09-8 (R)-2-amino-2-phenylpropanoic acid 
• 29738-04-3 (S)-(+)-2-cyano-2-methylphenylacetic acid 
• 682351-19-5 ((R)-1,2,2-Trimethoxy-1-methyl-ethyl)-benzene 
• 91899-79-5 (S)-2-methoxy-2-phenylpropanal 
• 121569-35-5 (S)-2-Chloro-2-phenyl-propionaldehyde 
• 24190-08-7 (R)-(-)-2-methoxy-2-phenylpropionic acid 

Relevant academic research and scientific papers

Stereospecific Construction of Chiral Quaternary α-Oxygenated Aldehydes from Chiral Secondary Alcohol Derivatives

Chiral tertiary dichloromethylcarbinol derivatives 2, prepared from protected chiral secondary alcohols 1, were converted stereospecifically into chiral quaternary α-oxygenated aldehyde derivatives 4 and 11 via intermediary α-chloroepoxides 3 under weakly

Stereospecific construction of chiral quaternary carbon compounds from chiral secondary alcohol derivatives

Chiral tertiary dichloromethylcarbinol derivatives, prepared by stereospecific α C-H insertion reaction of dichlorocarbene with protected chiral secondary alcohols, were converted into intermediary α-chloroepoxides which gave stereospecifically chiral qua