One-Pot Synthesis of 2-Indolyl-C-Glycosides

  • Author: ChemViews
  • Published Date: 06 December 2012
  • Source / Publisher: European Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: One-Pot Synthesis of 2-Indolyl-C-Glycosides

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C-aryl glycosides which are an important class of C-glycosides comprise a large number of biologically active natural products that have an aromatic ring linked to the anomeric carbon of a sugar through a C–C bond. Several methods are available for the synthesis of 2-indole derivatives, but there are only a few reports on the synthesis of 2- and 3-indolyl-C-glycosides. These mostly involve the addition of N-protected lithio-indoles onto sugar-derived lactones or lactols followed by reduction or cyclization.

Parthasarathi Subramanian and Krishna P. Kaliappan, Indian Institute of Technology, Mumbai, have accomplished the synthesis of a variety of N-tosyl-2-indolyl-C-glycosides through a cascade reaction of C-alkynyl glycosides that involves a sequential Sonogashir type coupling and cyclative-hydroamination. They also extended this strategy to develop a one-pot synthesis of 2-indolyl-C-glycosides through tetrabutylammonium fluoride (TBAF)-mediated removal of the N-tosyl group. Notable features of this syntehsis include tolerance to sensitive functional groups and the selective functionalization of sugar-derived bis-alkyne.

The method serves as a straightforward alternative for the synthesis of 2-indolyl-C-glycosides and also facilitates the synthesis of related natural products. Further efforts to extend the scope of this methodology will include the total synthesis of α-C-mannosyl-tryptophan and its analogues.

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