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Wang K, Yee CC, Au-Yeung HY. Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions. Chem Sci. 2016;7(4):2787-2792doi: 10.1039/c5sc04774a.
Wang, K., Yee, C. C., & Au-Yeung, H. Y. (2016). Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions. Chemical science, 7(4), 2787-2792. https://doi.org/10.1039/c5sc04774a
Wang, Kai, et al. "Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions." Chemical science vol. 7,4 (2016): 2787-2792. doi: https://doi.org/10.1039/c5sc04774a
Wang K, Yee CC, Au-Yeung HY. Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions. Chem Sci. 2016 Apr 21;7(4):2787-2792. doi: 10.1039/c5sc04774a. Epub 2016 Jan 15. PMID: 28660056; PMCID: PMC5477039.
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Chem Sci. 2016 Apr 21;7(4):2787-2792. doi: 10.1039/c5sc04774a. Epub 2016 Jan 15.

Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions.

Chemical science

Kai Wang, Chi-Chung Yee, Ho Yu Au-Yeung

Affiliations

  1. Department of Chemistry , The University of Hong Kong , Pokfulam Road , Hong Kong , P. R. China . Email: [email protected].

PMID: 28660056 PMCID: PMC5477039 DOI: 10.1039/c5sc04774a

Abstract

A water soluble [6]catenane consisting of two interlocking [3]catenanes was synthesised in 91% yield using readily accessible precursors. The new strategy features the simultaneous use of orthogonal Cu

References

  1. Chem Commun (Camb). 2007 Apr 7;(13):1369-71 - PubMed
  2. Angew Chem Int Ed Engl. 2012 Oct 1;51(40):10094-8 - PubMed
  3. J Am Chem Soc. 2012 Oct 17;134(41):17007-10 - PubMed
  4. Angew Chem Int Ed Engl. 2014 Oct 13;53(42):11261-5 - PubMed
  5. Org Biomol Chem. 2011 May 7;9(9):3504-15 - PubMed
  6. Nat Chem. 2014 Nov;6(11):978-82 - PubMed
  7. Angew Chem Int Ed Engl. 2015 Jun 22;54(26):7555-9 - PubMed
  8. J Am Chem Soc. 2003 Aug 6;125(31):9284-5 - PubMed
  9. J Phys Chem A. 2009 Feb 12;113(6):989-97 - PubMed
  10. Org Lett. 2015 Jun 5;17(11):2804-7 - PubMed
  11. Angew Chem Int Ed Engl. 2013 May 27;52(22):5749-52 - PubMed
  12. Chem Commun (Camb). 2014 Aug 4;50(60):8124-7 - PubMed
  13. J Am Chem Soc. 2014 Jun 11;136(23):8243-51 - PubMed
  14. Org Lett. 2009 Aug 6;11(15):3350-3 - PubMed
  15. J Am Chem Soc. 2013 Nov 27;135(47):17691-4 - PubMed
  16. Anal Chem. 2011 Oct 15;83(20):7916-23 - PubMed
  17. Angew Chem Int Ed Engl. 2014 Jul 21;53(30):7823-7 - PubMed
  18. Chem Commun (Camb). 2013 Feb 28;49(17):1679-95 - PubMed
  19. Angew Chem Int Ed Engl. 2011 Sep 26;50(40):9260-327 - PubMed
  20. Chem Soc Rev. 2010 Apr;39(4):1240-51 - PubMed
  21. Chem Soc Rev. 2013 Aug 21;42(16):6860-909 - PubMed
  22. Chem Commun (Camb). 2016 Jan 7;52(2):319-22 - PubMed
  23. Chemistry. 2012 Apr 27;18(18):5589-605 - PubMed
  24. J Am Chem Soc. 2002 Mar 13;124(10):2140-7 - PubMed
  25. Angew Chem Int Ed Engl. 2015 May 18;54(21):6110-50 - PubMed
  26. J Am Chem Soc. 2013 Feb 13;135(6):2084-7 - PubMed
  27. Chem Soc Rev. 2010 Jan;39(1):17-29 - PubMed
  28. Acc Chem Res. 2014 Jul 15;47(7):2041-51 - PubMed
  29. Chem Soc Rev. 2002 Mar;31(2):96-107 - PubMed
  30. Chem Rev. 2009 Nov;109(11):6024-46 - PubMed
  31. Chem Soc Rev. 2015 Feb 7;44(3):815-32 - PubMed
  32. J Am Chem Soc. 2014 Apr 23;136(16):5908-11 - PubMed
  33. Org Biomol Chem. 2015 Mar 14;13(10):2927-30 - PubMed
  34. Chem Soc Rev. 2014 Jul 7;43(13):4658-83 - PubMed
  35. Chemistry. 2009 Oct 12;15(40):10360-3 - PubMed
  36. Chemistry. 2008;14(13):4110-6 - PubMed
  37. Angew Chem Int Ed Engl. 1999 Mar 1;38(5):637-641 - PubMed

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