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Journal Abstract Search

147 related items for PubMed ID: 2990746

  • 1. Stereoselective reactions. VIII. Stereochemical requirement for the benzylic oxidation of lignan lactone. A highly selective synthesis of the antitumor lignan lactone steganacin by the oxidation of stegane.
    Ishiguro T, Mizuguchi H, Tomioka K, Koga K.
    Chem Pharm Bull (Tokyo); 1985 Feb; 33(2):609-17. PubMed ID: 2990746
    [No Abstract] [Full Text] [Related]

  • 2. Stereoselective reactions. XII. Synthesis of antitumor-active steganacin analogs, picrosteganol and epipicrosteganol, by selective isomerization.
    Tomioka K, Ishiguro T, Iitaka Y, Koga K.
    Chem Pharm Bull (Tokyo); 1986 Apr; 34(4):1501-4. PubMed ID: 3719859
    [No Abstract] [Full Text] [Related]

  • 3. Absolute structure-cytotoxic activity relationships of steganacin congeners and analogues.
    Tomioka K, Ishiguro T, Mizuguchi H, Komeshima N, Koga K, Tsukagoshi S, Tsuruo T, Tashiro T, Tanida S, Kishi T.
    J Med Chem; 1991 Jan; 34(1):54-7. PubMed ID: 1992152
    [Abstract] [Full Text] [Related]

  • 4. [Asymmetric total synthesis of some biologically active natural products].
    Tomioka K.
    Yakugaku Zasshi; 1984 Oct; 104(10):1009-23. PubMed ID: 6397584
    [No Abstract] [Full Text] [Related]

  • 5. Improved stereoselective synthesis of optically active methylene lactone, key intermediate for the synthesis of 1,2-oxidized furofuran lignan, by direct alpha-methylenation to butanolide.
    Yamauchi S, Yamamoto N, Kinoshita Y.
    Biosci Biotechnol Biochem; 2000 Oct; 64(10):2209-15. PubMed ID: 11129596
    [Abstract] [Full Text] [Related]

  • 6. alpha,beta-Dibenzyl-gamma-butyrolactone lignan alcohols: total synthesis of (+/-)-7'-hydroxyenterolactone, (+/-)-7'-hydroxymatairesinol and (+/-)-8-hydroxyenterolactone.
    Mäkelä TH, Kaltia SA, Wähälä KT, Hase TA.
    Steroids; 2001 Oct; 66(10):777-84. PubMed ID: 11522341
    [Abstract] [Full Text] [Related]

  • 7. Diversity oriented microwave-assisted synthesis of (-)-steganacin aza-analogues.
    Mont N, Mehta VP, Appukkuttan P, Beryozkina T, Toppet S, Van Hecke K, Van Meervelt L, Voet A, DeMaeyer M, Van der Eycken E.
    J Org Chem; 2008 Oct 03; 73(19):7509-16. PubMed ID: 18754579
    [Abstract] [Full Text] [Related]

  • 8. Stereoselectivity questions in the synthesis of wikstromol.
    Belletire JL, Ho DM, Fry DF.
    J Nat Prod; 1990 Oct 03; 53(6):1587-92. PubMed ID: 2089125
    [Abstract] [Full Text] [Related]

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  • 10. In vitro antitumor activities of new synthetic bistetrahydrofuran derivatives as analogs of Annonaceous acetogenins.
    Sasaki S, Maruta K, Naito H, Maemura R, Kawahara E, Maeda M.
    Chem Pharm Bull (Tokyo); 1998 Jan 03; 46(1):154-8. PubMed ID: 9468648
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  • 12. Synthesis of (+)-aptosimon, a 4-oxofurofuran lignan, by erythro selective aldol condensation and stereoconvergent cyclization as the key reactions.
    Yamauchi S, Yamaguchi M.
    Biosci Biotechnol Biochem; 2003 Apr 03; 67(4):838-46. PubMed ID: 12784626
    [Abstract] [Full Text] [Related]

  • 13. Selective Lewis acid catalyzed transformation (gamma-butyrolactone versus cyclopropane) of 2-methoxy-4-benzyltetrahydrofuran derivatives. Efficient synthesis of lignan lactones.
    Ferrié L, Bouyssi D, Balme G.
    Org Lett; 2005 Jul 21; 7(15):3143-6. PubMed ID: 16018606
    [Abstract] [Full Text] [Related]

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  • 15. Total synthesis of cis-reticulatacin-10-ones A and B: absolute stereochemical assignment.
    Abdel Ghani SB, Brown LJ, Figadère B, Brown RC.
    Org Biomol Chem; 2010 Oct 21; 8(20):4543-5. PubMed ID: 20733975
    [Abstract] [Full Text] [Related]

  • 16. Stereoselective synthesis of β-(hydroxymethylaryl/alkyl)-α-methylene-γ-butyrolactones.
    Hodgson DM, Talbot EP, Clark BP.
    Org Lett; 2011 May 20; 13(10):2594-7. PubMed ID: 21488628
    [Abstract] [Full Text] [Related]

  • 17. Modular Synthesis and Biological Investigation of 5-Hydroxymethyl Dibenzyl Butyrolactones and Related Lignans.
    Davidson SJ, Pilkington LI, Dempsey-Hibbert NC, El-Mohtadi M, Tang S, Wainwright T, Whitehead KA, Barker D.
    Molecules; 2018 Nov 22; 23(12):. PubMed ID: 30467285
    [Abstract] [Full Text] [Related]

  • 18. A protecting-group-free synthesis of (+)-nephrosteranic, (+)-protolichesterinic, (+)-nephrosterinic, (+)-phaseolinic, (+)-rocellaric acids and (+)-methylenolactocin.
    Nallasivam JL, Fernandes RA.
    Org Biomol Chem; 2017 Jan 18; 15(3):708-716. PubMed ID: 27995236
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  • 20. A bidirectional approach to the synthesis of a complete library of adjacent-bis-THF annonaceous acetogenins.
    Das S, Li LS, Abraham S, Chen Z, Sinha SC.
    J Org Chem; 2005 Jul 22; 70(15):5922-31. PubMed ID: 16018687
    [Abstract] [Full Text] [Related]

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