@article{discovery1474726,
          volume = {13},
           month = {June},
            year = {2015},
           title = {An improved transition-metal-free synthesis of aryl alkynyl sulfides via substitution of a halide at an sp-centre},
         journal = {Organic and Biomolecular Chemistry},
          number = {21},
            note = {This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.},
           pages = {5859--5861},
          author = {Chowdhury, RM and Wilden, JD},
        abstract = {A simple high-yielding preparation of aryl alkynyl sulfides is presented. The reaction of a chloroacetylene with a thiolate salt in the presence of an amine mediator (dimethylamine or N,N'-dimethylethylenediamine) yields the alkynyl sulfides in excellent yields. The alkynyl chloride is easily prepared from the parent alkyne.},
             url = {http://dx.doi.org/10.1039/c5ob00494b},
            issn = {1477-0539}
}