ruthenium-catalyzed cycloaddition of alkynes and organic azides

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2006 Triazole derivatives R 0280 Ruthenium-Catalyzed Cycloaddition of Alkynes and Organic Azides. 1,5-Disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles are prepared by the title reaction in good yields and with high regioselectivity. Together with the known Cu(I)-catalyzed azide—alkyne cycloaddition reaction affording 1,4-disubstituted 1,2,3-triazoles, both regioisomers of disubstituted 1,2,3-triazoles are available. — (ZHANG, L.; CHEN, X.; XUE, P.; SUN, H. H. Y.; WILLIAMS, I. D.; SHARPLESS, K. B.; FOKIN, V. V.; JIA*, G.; J. Am. Chem. Soc. 127 (2005) 46, 15998-15999; Dep. Chem., Hong Kong Univ. Sci. Technol., Kowloon, Hong Kong, Peop. Rep. China; Eng.) — Klein 12- 126

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Page 1: Ruthenium-Catalyzed Cycloaddition of Alkynes and Organic Azides

2006

Triazole derivativesR 0280 Ruthenium-Catalyzed Cycloaddition of Alkynes and Organic Azides. —

1,5-Disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles are prepared by the title reaction in good yields and with high regioselectivity. Together with the known Cu(I)-catalyzed azide—alkyne cycloaddition reaction affording 1,4-disubstituted 1,2,3-triazoles, both regioisomers of disubstituted 1,2,3-triazoles are available. — (ZHANG, L.; CHEN, X.; XUE, P.; SUN, H. H. Y.; WILLIAMS, I. D.; SHARPLESS, K. B.; FOKIN, V. V.; JIA*, G.; J. Am. Chem. Soc. 127 (2005) 46, 15998-15999; Dep. Chem., Hong Kong Univ. Sci. Technol., Kowloon, Hong Kong, Peop. Rep. China; Eng.) — Klein

12- 126