Shuaihu Geng , Jue Yang , Aleksander A. Lugovski , Weiping Liu
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引用次数: 0
Abstract
Herein, we report a highly efficient and selective formal C3-alkylation of indenes with a wide range of primary and secondary alcohols catalyzed by PNP-manganese pincer complex. This transformation proceeds via a borrowing hydrogen strategy, utilizing sustainable and abundant alcohols as alkylating agents. The reaction offers good functional group tolerance and regioselectivity, providing a practical and straightforward approach to the synthesis of alkylated indenes. Preliminary mechanistic investigations indicate that the reaction proceeds via a multi-step pathway involving the dehydrogenation of the alcohol to a carbonyl intermediate, followed by cross-condensation, hydrogenation, and isomerization steps to afford the final product.
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.