Stereoselective transformation of amines via chiral 2, 4, 6-triphenylpyridinium intermediates
SA Said, A Fiksdahl
Index: Said, Sadri A.; Fiksdahl, Anne Tetrahedron Asymmetry, 2001 , vol. 12, # 13 p. 1947 - 1951
Full Text: HTML
Citation Number: 4
Abstract
We herein report the preparation and the nucleophilic substitution of the chiral 2, 4, 6- triphenylpyridinium tetrafluoroborates 2a and 2b. The triphenylpyridinium intermediates were generated from homochiral amines (1a, 1b) and 2, 4, 6-triphenylpyrylium tetrafluoroborate and used as substrates for stereoselective nucleophilic substitution. The degree of inversion in the substitution reactions has been studied. The alcohol (3a, 3b) ...
Related Articles:
[Cazorla, Clement; Metay, Estelle; Lemaire, Marc Tetrahedron, 2011 , vol. 67, # 45 p. 8615 - 8621]
[De Oliveira Freitas, Luiza Baptista; Eisenberger, Patrick; Crudden, Cathleen M. Organometallics, 2013 , vol. 32, # 22 p. 6635 - 6638]
[Zheng, Hongchao; McDonald, Robert; Hall, Dennis G. Chemistry - A European Journal, 2010 , vol. 16, # 18 p. 5454 - 5460]
[Sawama, Yoshinari; Nagata, Saori; Yabe, Yuki; Morita, Kosuke; Monguchi, Yasunari; Sajiki, Hironao Chemistry - A European Journal, 2012 , vol. 18, # 52 p. 16608 - 16611]
[Sawama, Yoshinari; Nagata, Saori; Yabe, Yuki; Morita, Kosuke; Monguchi, Yasunari; Sajiki, Hironao Chemistry - A European Journal, 2012 , vol. 18, # 52 p. 16608 - 16611]