Synthesis of substituted 1-[2-(adamantan-1-yl)ethyl]piperidines

被引:0
作者
V. A. Shadrikova
E. V. Golovin
E. A. Kuznetsova
M. Yu. Rostova
Yu. N. Klimochkin
机构
[1] Samara State Technical University,
来源
Russian Journal of Organic Chemistry | 2016年 / 52卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Quaternary 1-[2-(adamantan-1-yl)ethyl]pyridinium bromides were reduced with sodium tetrahydridoborate in ethanol, and hydroarylation of the resulting 1-[2-(adamantan-1-yl)ethyl]-1,2,3,6-tetrahydropyridines with benzene in trifluoromethanesulfonic acid afforded phenylpiperidines with preferentially equatorial orientation of the phenyl substituent.
引用
收藏
页码:1452 / 1462
页数:10
相关论文
共 155 条
[31]  
Lamoureux G.(2002)undefined Magn. Reson. Chem. 40 549-undefined
[32]  
Artavi G.(1989)undefined Chirality 1 202-undefined
[33]  
Joubert J.(1982)undefined Org. Magn. Reson. 18 171-undefined
[34]  
Geldenhus W.J.(1986)undefined J. Med. Chem. 29 531-undefined
[35]  
van der Schyf C.J.(2013)undefined Tetrahedron 69 5867-undefined
[36]  
Oliver D.W.(2006)undefined J. Am. Chem. Soc. 128 6042-undefined
[37]  
Kruger H.G.(1989)undefined Magn. Reson. Chem. 27 964-undefined
[38]  
Govender T.(2015)undefined Can. J. Chem. 93 468-undefined
[39]  
Malan S.F.(1987)undefined Magn. Reson. Chem. 25 524-undefined
[40]  
Spasov A.A.(1981)undefined Magn. Reson. Chem. 15 275-undefined