BiCl3-mediated opening of epoxides, a facile route to chlorohydrins or amino alcohols: one reagent, two paths | NOVA. The University of Newcastle's Digital Repository

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.13/25329

Title: BiCl3-mediated opening of epoxides, a facile route to chlorohydrins or amino alcohols: one reagent, two paths
Author/Creator: McCluskey, Adam; Leitch, Sarah K.; Garner, James; Caden, Christine E.; Hill, Timothy A.; Odell, Luke R.; Stewart, Scott G.
Description: 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.
Relation: Tetrahedron Letters Vol. 46, no. 47, p. 8229-8232
Date: 2005
Publisher: Pergamon Press
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/25329
Identifier: ISSN:0040-4039
Language: eng

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