Regioselective Opening of Epoxides Catalyzed by Sn (IV). A New Method for the Synthesis of Halohydrins?

doi:10.3390/50300468

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Molecules 2000, 5(3), 468-469; doi:10.3390/50300468

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Regioselective Opening of Epoxides Catalyzed by Sn (IV). A New Method for the Synthesis of Halohydrins?

Claudio J. Salomon

Facultad de Cs. Bioquímicas y Farmacéuticas. IQUIOS-CONICET, Universidad Nacional de Rosario. Suipacha 531, 2000 Rosario, Argentina

Published: 22 March 2000

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Abstract: The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alcohols was developed, yielding the halohydrin derivatives.

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MDPI and ACS Style

Salomon, C.J. Regioselective Opening of Epoxides Catalyzed by Sn (IV). A New Method for the Synthesis of Halohydrins? Molecules 2000, 5, 468-469.

AMA Style

Salomon CJ. Regioselective Opening of Epoxides Catalyzed by Sn (IV). A New Method for the Synthesis of Halohydrins? Molecules. 2000; 5(3):468-469.

Chicago/Turabian Style

Salomon, Claudio J. 2000. "Regioselective Opening of Epoxides Catalyzed by Sn (IV). A New Method for the Synthesis of Halohydrins?" Molecules 5, no. 3: 468-469.

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