Molecules 2001, 6(9), 770-776; doi:10.3390/60900770

Niobium Pentachloride Catalysed Ring Opening of Epoxides

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Received: 11 June 2001; in revised form: 24 August 2001 / Accepted: 24 August 2001 / Published: 31 August 2001
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Epoxide ring opening is a frequently required transformation in Organic Synthesis. In this paper we describe the application of NbCl5 for this purpose using three different substrates. Chlorohydrins, 1,2-diols, products containing solvent residues as well as rearrangement products are obtained, depending on both the substrate structure and reaction conditions. Rationalizations to account for some of the results are suggested.
Keywords: Niobium pentachloride; Epoxides; 1; 2-Diols; Chlorohydrins
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MDPI and ACS Style

Constantino, M.G.; Lacerda, V., Jr.; Aragão, V. Niobium Pentachloride Catalysed Ring Opening of Epoxides. Molecules 2001, 6, 770-776.

AMA Style

Constantino MG, Lacerda V, Jr, Aragão V. Niobium Pentachloride Catalysed Ring Opening of Epoxides. Molecules. 2001; 6(9):770-776.

Chicago/Turabian Style

Constantino, Mauricio G.; Lacerda, Valdemar, Jr.; Aragão, Valquiria. 2001. "Niobium Pentachloride Catalysed Ring Opening of Epoxides." Molecules 6, no. 9: 770-776.

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