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Journal Abstract Search

271 related items for PubMed ID: 15104447

  • 1. Stereoselective synthesis of (-)-cephalotaxine and C-7 alkylated analogues.
    Planas L, Pérard-Viret J, Royer J.
    J Org Chem; 2004 Apr 30; 69(9):3087-92. PubMed ID: 15104447
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  • 2. Stereoselectivity in N-Iminium Ion Cyclization: Development of an Efficient Synthesis of (±)-Cephalotaxine.
    Liu H, Yu J, Li X, Yan R, Xiao JC, Hong R.
    Org Lett; 2015 Sep 18; 17(18):4444-7. PubMed ID: 26332648
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  • 3. Convergency and divergency as strategic elements in total synthesis: the total synthesis of (-)-drupacine and the formal total synthesis of (+/-)-cephalotaxine, (-)-cephalotaxine, and (+)-cephalotaxine.
    Liu Q, Ferreira EM, Stoltz BM.
    J Org Chem; 2007 Sep 14; 72(19):7352-8. PubMed ID: 17705540
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  • 4. A formal synthesis of (-)-cephalotaxine.
    Esmieu WR, Worden SM, Catterick D, Wilson C, Hayes CJ.
    Org Lett; 2008 Jul 17; 10(14):3045-8. PubMed ID: 18549234
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  • 5. Asymmetric synthesis of spiroketal, spiroether, and oxabicycle building blocks via stereoselective spiro- and bicycloannulation of 2-hydroxy dihydropyrans.
    Lejkowski M, Banerjee P, Runsink J, Gais HJ.
    Org Lett; 2008 Jul 03; 10(13):2713-6. PubMed ID: 18512930
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  • 6. Synthesis of tert-butyl 6-oxo-2-azaspiro[3.3]heptane-2-carboxylate.
    Meyers MJ, Muizebelt I, van Wiltenburg J, Brown DL, Thorarensen A.
    Org Lett; 2009 Aug 20; 11(16):3523-5. PubMed ID: 19637855
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  • 8. Asymmetric, stereocontrolled total synthesis of paraherquamide A.
    Williams RM, Cao J, Tsujishima H, Cox RJ.
    J Am Chem Soc; 2003 Oct 08; 125(40):12172-8. PubMed ID: 14519003
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  • 13. Asymmetric aza-Wittig reactions: enantioselective synthesis of beta-quaternary azacycles.
    Lertpibulpanya D, Marsden SP, Rodriguez-Garcia I, Kilner CA.
    Angew Chem Int Ed Engl; 2006 Jul 24; 45(30):5000-2. PubMed ID: 16819749
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  • 15. A second generation formal synthesis of (-)-cephalotaxine.
    Hameed A, Blake AJ, Hayes CJ.
    J Org Chem; 2008 Oct 17; 73(20):8045-8. PubMed ID: 18785776
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  • 16. Highly efficient formal synthesis of cephalotaxine, using the Stevens rearrangement--acid lactonization sequence as a key transformation.
    Sun MR, Lu HT, Wang YZ, Yang H, Liu HM.
    J Org Chem; 2009 Mar 06; 74(5):2213-6. PubMed ID: 19170601
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  • 18. A new general approach for the stereocontrolled synthesis of functionalised γ- and δ-lactams.
    Daly M, Gill K, Sime M, Simpson GL, Sutherland A.
    Org Biomol Chem; 2011 Oct 07; 9(19):6761-70. PubMed ID: 21837339
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  • 20. Asymmetric total synthesis of pinnaic acid.
    Xu S, Arimoto H, Uemura D.
    Angew Chem Int Ed Engl; 2007 Oct 07; 46(30):5746-9. PubMed ID: 17592606
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