371785-35-2Relevant academic research and scientific papers
Diastereoselective synthesis of trans-N-benzyl-2-(2-methylphenyl)-6-phenyl-4-piperidone
Ishimaru, Kaori,Kojima, Takakazu
, p. 1591 - 1597 (2007/10/03)
Diastereoselective synthesis of trans-N-benzyl-2-(2-methylphenyl)-6-phenyl-4-piperidone (6a) was performed by cycloaddition of the aldimine (1c) with 2-silyloxy-l,3-butadiene in the presence of trimethylsilyl triflate. The use of the p-trimethylsilyl substituent of the aromatic ring of the aldimine gave high diastereoselectivity of the product.
