131023-34-2

Upstream product

• 133412-37-0 Acetic acid 4-[(R)-cyano-((E)-(S)-1-methyl-but-2-enyloxy)-methyl]-phenyl ester 
• 133412-39-2 Acetic acid 4-[(R)-cyano-((S)-1-methyl-butoxy)-methyl]-phenyl ester 
• 134983-50-9 (R)-2-hydroxy-2-(4-acetylphenyl)acetonitrile 
• 1569-50-2 3-penten-2-ol 
• 62918-50-7 4-(4-octoxyphenyl)benzoyl chloride 
• 133412-41-6 (R)-(4-Hydroxy-phenyl)-((S)-1-methyl-butoxy)-acetonitrile 
• 133412-37-0 Acetic acid 4-[(R)-cyano-((E)-(R)-1-methyl-but-2-enyloxy)-methyl]-phenyl ester 
• 133412-39-2 Acetic acid 4-[(R)-cyano-((R)-1-methyl-butoxy)-methyl]-phenyl ester 
• 133412-41-6 (R)-(4-Hydroxy-phenyl)-((R)-1-methyl-butoxy)-acetonitrile 
• 133412-46-1 1-Methyl-2-butenyl trichloroacetoimidate 

Relevant academic research and scientific papers

Synthesis of optically active α-cyanobenzyl alkyl ethers

The title ethers, expected chiral dopants for ferroelectric liquid crystals, were prepared by the allylation of chiral cyanohydrins under the acidic conditions followed by hydrogenation, or alternatively by the Johnson's cyanation of chiral acetals follow