Microwave-enhanced bismuth triflate-catalyzed epoxide opening with aliphatic amines
T Ollevier, E Nadeau
Index: Ollevier, Thierry; Nadeau, Etienne Tetrahedron Letters, 2008 , vol. 49, # 9 p. 1546 - 1550
Full Text: HTML
Citation Number: 33
Abstract
In the presence of a catalytic amount of Bi (OTf) 3· 4H2O and under microwave irradiation, neat mixtures of epoxides and amines afforded smoothly the corresponding 2-amino alcohols. A wide variety of aliphatic amines were reacted with cycloalkene oxide, styrene oxide, and stilbene oxide. The reaction proceeded rapidly and afforded the 2-amino alcohols in high up to quantitative yields. All products could be obtained without aqueous ...
Related Articles:
[Goralski, Christian T.; Singaram, Bakthan; Brown, Herbert C. Journal of Organic Chemistry, 1987 , vol. 52, # 18 p. 4014 - 4019]
[Fisher, Gary B.; Goralski, Christian T.; Nicholson, Lawrence W.; Hasha, Dennis L.; Zakett, Donald; Singaram, Bakthan Journal of Organic Chemistry, 1995 , vol. 60, # 7 p. 2026 - 2034]
[Goralski, Christian T.; Singaram, Bakthan; Brown, Herbert C. Journal of Organic Chemistry, 1987 , vol. 52, # 18 p. 4014 - 4019]