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Pure Appl. Chem., 2003, Vol. 75, No. 1, pp. 63-70

http://dx.doi.org/10.1351/pac200375010063

Unified strategy for the synthesis of C-aryl glycosides

S. F. Martin

Department of Chemistry and Biochemistry, The University of Texas, Austin, TX 78712, USA

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  • Bartholomäus Ruben, Bachmann Janina, Mang Christian, Haustedt Lars Ole, Harms Klaus, Koert Ulrich: Synthesis of the AB-Ring Pyranolactone Substructure of Granaticin A. Eur. J. Org. Chem. 2013, 2013, 180. <http://dx.doi.org/10.1002/ejoc.201201279>
  • Miller Justin N., Pongdee Rongson: An efficient and cost-effective preparation of di-O-acetyl-d-rhamnal. Tetrahedron Letters 2013, 54, 3185. <http://dx.doi.org/10.1016/j.tetlet.2013.04.035>
  • Nicolas Lionel, Izquierdo Eva, Angibaud Patrick, Stansfield Ian, Meerpoel Lieven, Reymond Sébastien, Cossy Janine: Cobalt-Catalyzed Diastereoselective Synthesis of C-Furanosides. Total Synthesis of (−)-Isoaltholactone. J. Org. Chem. 2013, 78, 11807. <http://dx.doi.org/10.1021/jo401845q>
  • Nicolas Lionel, Angibaud Patrick, Stansfield Ian, Bonnet Pascal, Meerpoel Lieven, Reymond Sébastien, Cossy Janine: Diastereoselective Metal-Catalyzed Synthesis of C -Aryl and C -Vinyl Glycosides. Angew. Chem. 2012, 124, 11263. <http://dx.doi.org/10.1002/ange.201204786>
  • Nicolas Lionel, Angibaud Patrick, Stansfield Ian, Bonnet Pascal, Meerpoel Lieven, Reymond Sébastien, Cossy Janine: Diastereoselective Metal-Catalyzed Synthesis of C -Aryl and C -Vinyl Glycosides. Angew. Chem. Int. Ed. 2012, 51, 11101. <http://dx.doi.org/10.1002/anie.201204786>
  • Cobo Isidro, Matheu M. Isabel, Castillón Sergio, Boutureira Omar, Davis Benjamin G.: Phosphine-Free Suzuki–Miyaura Cross-Coupling in Aqueous Media Enables Access to 2-C-Aryl-Glycosides. Z Org Lett 2012, 14, 1728. <http://dx.doi.org/10.1021/ol3003139>
  • Fosso Marina Y., Nziko V. P. N., Chang Cheng-Wei Tom: Chemical Synthesis of N-Aryl Glycosides. Journal of Carbohydrate Chemistry 2012, 31, 603. <http://dx.doi.org/10.1080/07328303.2012.699575>
  • López J. Cristóbal, Plumet Joaquín: Metathesis Reactions of Carbohydrates: Recent Highlights in Alkyne Metathesis. Eur J Org Chem 2011, 2011, 1803. <http://dx.doi.org/10.1002/ejoc.201001518>
  • O’Keefe B. Michael, Mans Douglas M., Kaelin David E., Martin Stephen F.: Studies toward the syntheses of pluramycin natural products. The first total synthesis of isokidamycin. Tetrahedron 2011, 67, 6524. <http://dx.doi.org/10.1016/j.tet.2011.05.117>
  • Subrahmanyam Ayyagari V., Palanichamy Kalanidhi, Kaliappan Krishna P.: Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C-Aryl Glycosides and Spiro-C-Aryl Glycosides. Chem Eur J 2010, 16, 8545. <http://dx.doi.org/10.1002/chem.201000482>
  • De Castro Michael, Marzabadi Cecilia H.: Preparation and reactions of iodo sugars. Tetrahedron 2010, 66, 3395. <http://dx.doi.org/10.1016/j.tet.2010.03.001>
  • O’Keefe B. Michael, Mans Douglas M., Kaelin David E., Martin Stephen F.: Total Synthesis of Isokidamycin. J Am Chem Soc 2010, 132, 15528. <http://dx.doi.org/10.1021/ja107926f>
  • Sparks Steven M., Chen Chi-Li, Martin Stephen F.: Tandem intramolecular benzyne–furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. Tetrahedron 2007, 63, 8619. <http://dx.doi.org/10.1016/j.tet.2007.04.031>
  • Procko Kristen, Martin Stephen F., Li Hui: Facile synthesis of C-aryl glycals from sugar-derived lactones. Tetrahetron Lett 2006, 47, 3485. <http://dx.doi.org/10.1016/j.tetlet.2006.02.150>
  • Parker Kathlyn A., Su Dai‐Shi: Models for the Synthesis of Pluramycin Antibiotics. Rearrangement of Mono‐Protected Aminoglycal‐Substituted Cyclohexadienediols. J Carbohydr Chem 2005, 24, 199. <http://dx.doi.org/10.1081/CAR-200059936>