Literature DB >> 20073529

Room temperature direct alkynylation of 1,3,4-oxadiazoles with alkynyl bromides under copper catalysis.

Tsuyoshi Kawano1, Naoto Matsuyama, Koji Hirano, Tetsuya Satoh, Masahiro Miura.   

Abstract

The direct alkynylation reaction of 1,3,4-oxadiazoles with alkynyl bromides efficiently proceeds in the presence of a copper catalyst at room temperature to create the corresponding heteroaryl-alkynyl linkage in good yields. This direct coupling provides a rapid and convergent access to oxadiazole core pi-conjugated systems.

Entities:  

Year:  2010        PMID: 20073529     DOI: 10.1021/jo9025622

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Ligand-free Pd/Ag-mediated dehydrogenative alkynylation of imidazole derivatives.

Authors:  Fabio Bellina; Matteo Biagetti; Sara Guariento; Marco Lessi; Mattia Fausti; Paolo Ronchi; Elisabetta Rosadoni
Journal:  RSC Adv       Date:  2021-07-22       Impact factor: 3.361

2.  Copper-catalyzed CuAAC/intramolecular C-H arylation sequence: Synthesis of annulated 1,2,3-triazoles.

Authors:  Rajkumar Jeyachandran; Harish Kumar Potukuchi; Lutz Ackermann
Journal:  Beilstein J Org Chem       Date:  2012-10-16       Impact factor: 2.883

  2 in total

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