Literature DB >> 26347490

Synthesis and application of a dual chiral [2.2]paracyclophane-based N-heterocyclic carbene in enantioselective β-boration of acyclic enones.

Lei Wang1, Zhen Chen1, Manyuan Ma2, Wenzeng Duan3, Chun Song2, Yudao Ma1.   

Abstract

An enantioselective conjugate addition of boron to α,β-unsaturated ketones catalysed by either a N-heterocyclic carbene or a copper-carbene complex generated in situ from a new chiral bicyclic triazolium based on [2.2]paracyclophane is presented. The dual chiral carbene-copper catalyst has significant advantages over its carbene counterpart as an organocatalyst in asymmetric β-boration of acyclic enones, giving a variety of chiral β-boryl ketones in good yields and enantioselectivities. This is a successful example of employing the same N-heterocyclic carbene in one catalytic reaction as both an organocatalyst and a ligand for transition metal catalysis.

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Year:  2015        PMID: 26347490     DOI: 10.1039/c5ob01609f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2022-04-27       Impact factor: 12.779

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Journal:  ChemistryOpen       Date:  2018-05-25       Impact factor: 2.911

  2 in total

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