SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Matthew R. Wilson, Richard E. Taylor, Gespannte Moleküle in der Naturstoffsynthese, Angewandte Chemie, 2013, 125, 15
  2. 2
    Matthew R. Wilson, Richard E. Taylor, Strained Alkenes in Natural Product Synthesis, Angewandte Chemie International Edition, 2013, 52, 15
  3. 3
    Jason Poulin, Christiane M. Grisé-Bard, Louis Barriault, A Formal Synthesis of Vinigrol, Angewandte Chemie, 2012, 124, 9
  4. 4
    Jason Poulin, Christiane M. Grisé-Bard, Louis Barriault, A Formal Synthesis of Vinigrol, Angewandte Chemie International Edition, 2012, 51, 9
  5. 5
    Henning Hopf, Michael S. Sherburn, Dendralene auf dem Vormarsch: kreuzkonjugierte Oligoene ermöglichen den schnellen Aufbau molekularer Komplexität, Angewandte Chemie, 2012, 124, 10
  6. 6
    Henning Hopf, Michael S. Sherburn, Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity, Angewandte Chemie International Edition, 2012, 51, 10
  7. 7
    Elizabeth H. Krenske, Emma W. Perry, Steven V. Jerome, Thomas J. Maimone, Phil S. Baran, K. N. Houk, Why a Proximity-Induced Diels–Alder Reaction Is So Fast, Organic Letters, 2012, 14, 12, 3016

    CrossRef

  8. 8
    K.-i. Tadano, Comprehensive Chirality, 2012,

    CrossRef

  9. 9
    Luiz F. Silva, Jr., Berit Olofsson, Hypervalent iodine reagents in the total synthesis of natural products, Natural Product Reports, 2011, 28, 10, 1722

    CrossRef

  10. 10
    Judith Hierold, Tina Hsia, David W. Lupton, The Grob/Eschenmoser fragmentation of cycloalkanones bearing β-electron withdrawing groups: a general strategy to acyclic synthetic intermediates, Organic & Biomolecular Chemistry, 2011, 9, 3, 783

    CrossRef

  11. 11
    Jin-Yong Lu, Dennis G. Hall, Fragmentation Enables Complexity in the First Total Synthesis of Vinigrol, Angewandte Chemie International Edition, 2010, 49, 13
  12. 12
    Our choice from the recent literature, Nature Chemistry, 2010, 2, 1, 4

    CrossRef

  13. 13
    Nadale K. Downer-Riley, Yvette A. Jackson, Synthesis highlights, Annual Reports Section "B" (Organic Chemistry), 2010, 106, 174

    CrossRef

  14. 14
    Kathrin Prantz, Johann Mulzer, Synthesis of (Z)-Trisubstituted Olefins by Decarboxylative Grob-Type Fragmentations: Epothilone D, Discodermolide, and Peloruside A, Chemistry - A European Journal, 2010, 16, 2
  15. You have free access to this content15
    Alexander D. Huters, Neil K. Garg, Synthetic Studies Inspired by Vinigrol, Chemistry - A European Journal, 2010, 16, 29
  16. 16
    Jin-Yong Lu, Dennis G. Hall, Totalsynthese von Vinigrol: Komplexität durch Fragmentierung, Angewandte Chemie, 2010, 122, 13
  17. 17
    Jason G.M. Morton, Laura D. Kwon, John D. Freeman, Jon T. Njardarson, An Adler–Becker oxidation approach to vinigrol, Tetrahedron Letters, 2009, 50, 15, 1684

    CrossRef

  18. 18
    Kathrin Prantz, Johann Mulzer, Decarboxylative Grob-Type Fragmentations in the Synthesis of Trisubstituted Z Olefins: Application to Peloruside A, Discodermolide, and Epothilone D, Angewandte Chemie International Edition, 2009, 48, 27
  19. 19
    Kathrin Prantz, Johann Mulzer, Decarboxylierende Grob-Fragmentierung zur Synthese trisubstituierter Z-Olefine: Anwendung auf Pelorusid A, Discodermolid und Epothilon D, Angewandte Chemie, 2009, 121, 27
  20. 20
    James R. Hanson, Diterpenoids, Natural Product Reports, 2009, 26, 9, 1156

    CrossRef

  21. 21
    Martin Juhl, David Tanner, Recent applications of intramolecular Diels–Alder reactions to natural product synthesis, Chemical Society Reviews, 2009, 38, 11, 2983

    CrossRef

  22. 22
    Thomas J. Maimone, Jun Shi, Shinji Ashida, Phil S. Baran, Total Synthesis of Vinigrol, Journal of the American Chemical Society, 2009, 131, 47, 17066

    CrossRef

  23. 23
    Laura Croft, Total synthesis: Vinigrol vanquished, Nature Chemistry, 2009,

    CrossRef

  24. 24
    Thomas J. Maimone, Ana-Florina Voica, Phil S. Baran, ChemInform Abstract: A Concise Approach to Vinigrol., ChemInform, 2008, 39, 33