Title of article :
Synthesis of diarylazepan-4-ones
Author/Authors :
Chang، نويسنده , , Meng-Yang and Kung، نويسنده , , Yung-Hua and Ma، نويسنده , , Chih-Chong، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Abstract :
Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement.
Keywords :
Grignard addition/dehydration , Boron trifluoride etherate , Epoxidation/pinacol rearrangement , Diarylazepan-4-ones , m-Chloroperoxybenzoic acid
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters