4.7 Article

Catalyst-controlled divergence in cycloisomerisation reactions of N-propargyl-N-vinyl sulfonamides: gold-catalysed synthesis of 2-sulfonylmethyl pyrroles and dihydropyridines

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CHEMICAL COMMUNICATIONS
卷 51, 期 72, 页码 13748-13751

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc04871k

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  1. Department of Science and Technology (DST), India
  2. DST
  3. XIIth five year plan project Affordable Cancer Therapeutics (ACT)
  4. Council of Scientific and Industrial Research (CSIR), India

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Gold-catalysed, divergent synthesis of 2-sulfonylmethyl pyrroles and dihydropyridines from N-propargyl-N-vinyl sulfonamides has been achieved. Echavarren's gold(I) catalyst promoted the formation of pyrrole derivatives whereas the combination of PPh3AuCl and AgSbF6 afforded dihydropyridines. The aza-enyne precursors for the cyclo-isomerisation reaction were prepared by a base-mediated formal vinylic substitution reaction of 2-bromoallyl sulfones.

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