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Collect. Czech. Chem. Commun. 2009, 74, 771-783
https://doi.org/10.1135/cccc2008195
Published online 2009-04-08 10:24:59

Sulfanylation of 1,3-dithiane anions by 5-(alkylsulfanyl)-1-phenyltetrazoles

Venugopal Gudipati, Reena Bajpai and Dennis P. Curran*

Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA

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  • Ghosh Arun K., Yuan Hao: Total Syntheses of the Proposed Structure of Iriomoteolide-1a, -1b and Synthesis of Three Derivatives for Structural Studies. Marine Drugs 2022, 20, 587. <https://doi.org/10.3390/md20100587>
  • Friedrich Ryan M., Friestad Gregory K.: Inspirations from tetrafibricin and related polyketides: new methods and strategies for 1,5-polyol synthesis. Nat. Prod. Rep. 2020, 37, 1229. <https://doi.org/10.1039/C9NP00070D>
  • Friedrich Ryan M., Bell Jay Q., Garcia Alfredo, Shen Zican, Friestad Gregory K.: Unified Strategy for 1,5,9- and 1,5,7-Triols via Configuration-Encoded 1,5-Polyol Synthesis: Preparation and Coupling of C15–C25 and C26–C40 Fragments of Tetrafibricin. J. Org. Chem. 2018, 83, 13650. <https://doi.org/10.1021/acs.joc.8b02034>
  • Friedrich Ryan M., Friestad Gregory K.: Access to an anti,syn‐1,5,7‐Triol by Configuration‐Encoded 1,5‐Polyol Synthesis: The C15–C25 Fragment of Tetrafibricin. Eur J Org Chem 2017, 2017, 1961. <https://doi.org/10.1002/ejoc.201700373>
  • Itoh Takahiko, Montgomery T. Patrick, Recio Antonio, Krische Michael J.: Asymmetric Alcohol C–H Allylation and syn-Crotylation: C9–C20 of Tetrafibricin. Org. Lett. 2014, 16, 820. <https://doi.org/10.1021/ol403566w>
  • Nuhant Philippe, Roush William R.: Enantio- and Diastereoselective Synthesis of N-Acetyl Dihydrotetrafibricin Methyl Ester. J. Am. Chem. Soc. 2013, 135, 5340. <https://doi.org/10.1021/ja401918r>
  • Nuhant Philippe, Kister Jeremy, Lira Ricardo, Sorg Achim, Roush William R.: Development of a double allylboration reagent targeting 1,5-syn-(E)-diols: application to the synthesis of the C(23)–C(40) fragment of tetrafibricin. Tetrahedron 2011, 67, 6497. <https://doi.org/10.1016/j.tet.2011.06.008>
  • Gudipati Venugopal, Curran Dennis P.: Synthesis of C1–C20 and C21–C40 fragments of tetrafibricin. Tetrahedron Letters 2011, 52, 2254. <https://doi.org/10.1016/j.tetlet.2011.01.086>
  • Kister Jeremy, Nuhant Philippe, Lira Ricardo, Sorg Achim, Roush William R.: Enantio- and Diastereoselective Synthesis of (E)-1,5-syn-Diols: Application to the Synthesis of the C(23)−C(40) Fragment of Tetrafibricin. Org. Lett. 2011, 13, 1868. <https://doi.org/10.1021/ol2003836>
  • Friestad Gregory K., Sreenilayam Gopeekrishnan: 1,5-Polyols: Challenging motifs for configurational assignment and synthesis. Pure and Applied Chemistry 2011, 83, 461. <https://doi.org/10.1351/PAC-CON-10-10-19>
  • Gudipati Venugopal, Bajpai Reena, Curran Dennis P.: ChemInform Abstract: Sulfanylation of 1,3‐Dithiane Anions by 5‐(Alkylsulfanyl)‐1‐phenyltetrazoles. ChemInform 2009, 40. <https://doi.org/10.1002/chin.200946158>