BiCl3-Mediated Opening of Epoxides, a Facile Route to Chlorohydrins or Amino Alcohols: One Reagent, Two Paths
Autor: | James Garner, Luke R. Odell, Adam McCluskey, Timothy A. Hill, Christine E. Caden, Scott G. Stewart, Sarah K. Leitch |
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Rok vydání: | 2006 |
Předmět: | |
Zdroj: | ChemInform. 37 |
ISSN: | 1522-2667 0931-7597 |
Popis: | 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. (c) 2005 Elsevier Ltd. All rights reserved. |
Databáze: | OpenAIRE |
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