Literature DB >> 29808531

Cu(I)-Catalyzed Cross-Coupling of Diazo Compounds with Terminal Alkynes: An Efficient Access to Allenes.

Mohammad Lokman Hossain1, Jianbo Wang2.   

Abstract

Cu(I)-catalyzed reaction of diazo compounds generates a Cu(I)-carbene intermediate that undergoes diverse transformations. In the past few years, the diazo compounds (or their precursor N-tosylhydrazones) have been established as cross-coupling partners under transition-metal catalysis, affording various organic compounds. Particularly the breakthrough has been made in allene synthesis by Cu(I)-catalyzed carbene coupling with terminal alkynes. Moreover, the Cu(I)-catalyzed coupling reaction of diazo compounds with terminal alkynes generates allene intermediate that undergoes tandem cyclization/coupling to afford cyclic compounds. This review article summarizes the most recent developments in allene synthesis based on the Cu(I)-carbene coupling reactions and the utilization of allene intermediates in tandem reactions.
© 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  allene synthesis; carbene; copper catalysis; cross-coupling; diazo compounds

Year:  2018        PMID: 29808531     DOI: 10.1002/tcr.201800023

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  2 in total

Review 1.  Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates.

Authors:  Kuiyong Dong; Mengting Liu; Xinfang Xu
Journal:  Molecules       Date:  2022-05-11       Impact factor: 4.927

2.  Catalytic enantioselective allene-anhydride approach to β,γ-unsaturated enones bearing an α-all-carbon-quarternary center.

Authors:  Yuan Yuan; Xue Zhang; Hui Qian; Shengming Ma
Journal:  Chem Sci       Date:  2020-07-22       Impact factor: 9.825

  2 in total

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