2010Chemistry - A European JournalOpen access

Multiple‐Organocatalyst‐Promoted Cascade Reaction: A Fast and Efficient Entry into Fully Substituted Piperidines

Yao Wang, De‐Feng Yu, Yao‐Zong Liu, Hao Wei, Yong‐Chun Luo, Darren J. Dixon, Peng‐Fei Xu

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Abstract

Multiple reactions in a single pot: The development of a catalytic asymmetric approach to fully substituted piperidines, which previously remained elusive, is achieved by the use of a multi-catalyst-promoted cascade reaction (see scheme). The one-pot reaction cascade is easy to perform, highly stereoselective and broad in scope, and the reaction products are high-value intermediates for multiple synthetic transformations.

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What this paper is about

Multiple reactions in a single pot: The development of a catalytic asymmetric approach to fully substituted piperidines, which previously remained elusive, is achieved by the use of a multi-catalyst-promoted cascade reaction (see scheme). The one-pot reaction cascade is easy to perform, highly stereoselective and broad in scope, and the reaction products are high-value intermediates for multiple synthetic transformations.

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Available abstract

Multiple reactions in a single pot: The development of a catalytic asymmetric approach to fully substituted piperidines, which previously remained elusive, is achieved by the use of a multi-catalyst-promoted cascade reaction (see scheme). The one-pot reaction cascade is easy to perform, highly stereoselective and broad in scope, and the reaction products are high-value intermediates for multiple synthetic transformations.

Key concepts: Cascade, Cascade reaction, Stereoselectivity, Catalysis, Combinatorial chemistry, Chemistry, Scope (computer science), Reaction conditions

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