Palladium-catalyzed denitrogenative cycloadditions and alkenylations of benzotriazoles with alkynes

Literature Information

Publication Date 2018-08-24
DOI 10.1039/C8QO00778K
Impact Factor 5.281
Authors

Yuanhao Wang, Zhiguo Wang, Xuewei Chen


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Abstract

The palladium-catalyzed denitrogenative formal [2 + 2 + 1]- and [2 + 2 + 2]-cycloadditions of benzotriazoles with internal alkynes have been achieved under different reaction conditions, which enable the efficient access of highly substituted 5,6-spiro bicycles and naphthalenes, respectively. In addition, the palladium-catalyzed denitrogenative alkenylations of benzotriazoles with terminal alkynes are also reported, which offers an efficient method to access ortho-amino styrenes. The present work shows that benzotriazoles could serve as capable precursors for the divergent syntheses of various valuable scaffolds.

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