Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.13/25329
- BiCl3-mediated opening of epoxides, a facile route to chlorohydrins or amino alcohols: one reagent, two paths
Leitch, Sarah K.;
Caden, Christine E.;
Hill, Timothy A.;
Odell, Luke R.;
Stewart, Scott G.
- Opening of epoxides can be an effective means by which a variety of functional groups can be incorporated. In this letter, we outline how variation of conditions, in particular, that of solvent and concentration, give rise to different products using the Lewis acid catalyst BiCl3.
- Tetrahedron Letters Vol. 46, no. 47, p. 8229-8232
- Pergamon Press
- Resource Type
- journal article