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Journal Abstract Search

124 related items for PubMed ID: 25103476

  • 1.
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  • 2. Bioinspired Asymmetric Synthesis of (-)-Gymnothelignan V.
    Soorukram D, Pohmakotr M, Kuhakarn C, Reutrakul V.
    J Org Chem; 2018 Apr 06; 83(7):4173-4179. PubMed ID: 29498520
    [Abstract] [Full Text] [Related]

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  • 4. Regiodivergent synthesis of trisubstituted furans through Tf(2)O-catalyzed Friedel-Crafts acylation: a tool for access to tetrahydrofuran lignan analogues.
    Comegna D, DellaGreca M, Rosaria Iesce M, Previtera L, Zarrelli A, Zuppolini S.
    Org Biomol Chem; 2012 Feb 14; 10(6):1219-24. PubMed ID: 22179391
    [Abstract] [Full Text] [Related]

  • 5. Use of the benzyl mesylate for the synthesis of tetrahydrofuran lignan: syntheses of 7,8-trans, 7',8'-trans, 7,7'-cis, and 8,8'-cis-virgatusin stereoisomers.
    Yamauchi S, Nakato T, Tsuchiya M, Akiyama K, Maruyama M, Sugahara T, Kishida T.
    Biosci Biotechnol Biochem; 2007 Sep 14; 71(9):2248-55. PubMed ID: 17827688
    [Abstract] [Full Text] [Related]

  • 6. Enantioselective Synthesis of a Furan Lignan (+)-Sylvone.
    Lee E, Bang J, Kwon J, Yu CM.
    J Org Chem; 2015 Oct 16; 80(20):10359-63. PubMed ID: 26414201
    [Abstract] [Full Text] [Related]

  • 7. First asymmetric synthesis of (-)-lintetralin via intramolecular Friedel-Crafts-type cyclization.
    Enders D, Del Signore G, Berner OM.
    Chirality; 2003 Jun 16; 15(6):510-3. PubMed ID: 12774291
    [Abstract] [Full Text] [Related]

  • 8. First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan.
    Yamauchi S, Okazaki M, Akiyama K, Sugahara T, Kishida T, Kashiwagi T.
    Org Biomol Chem; 2005 May 07; 3(9):1670-5. PubMed ID: 15858648
    [Abstract] [Full Text] [Related]

  • 9. Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.
    Nakato T, Yamauchi S.
    J Nat Prod; 2007 Oct 07; 70(10):1588-92. PubMed ID: 17887723
    [Abstract] [Full Text] [Related]

  • 10. First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol.
    Yamauchi S, Kinoshita Y.
    Biosci Biotechnol Biochem; 2001 Jul 07; 65(7):1559-67. PubMed ID: 11515539
    [Abstract] [Full Text] [Related]

  • 11. Synthesis of optically active olivil type of lignan from L-arabinose using threo-selective aldol condensation as a key reaction.
    Yamauchi S, Kinoshita Y.
    Biosci Biotechnol Biochem; 2000 Nov 07; 64(11):2320-7. PubMed ID: 11193398
    [Abstract] [Full Text] [Related]

  • 12. Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
    Jagtap PR, Císařová I, Jahn U.
    Org Biomol Chem; 2018 Jan 31; 16(5):750-755. PubMed ID: 29308468
    [Abstract] [Full Text] [Related]

  • 13.
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  • 14. 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 31; 67(4):838-46. PubMed ID: 12784626
    [Abstract] [Full Text] [Related]

  • 15. Enantioselective total synthesis of the lignan (+)-linoxepin.
    Tietze LF, Clerc J, Biller S, Duefert SC, Bischoff M.
    Chemistry; 2014 Dec 15; 20(51):17119-24. PubMed ID: 25345835
    [Abstract] [Full Text] [Related]

  • 16. Stereoselective synthesis of 3-alkyl-2-aryltetrahydrofuran-4-ols: total synthesis of (+/-)-paulownin.
    Angle SR, Choi I, Tham FS.
    J Org Chem; 2008 Aug 15; 73(16):6268-78. PubMed ID: 18646863
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  • 18. Stereocontrolled total synthesis of hedyotol A.
    Kawabe Y, Ishikawa R, Akao Y, Yoshida A, Inai M, Asakawa T, Hamashima Y, Kan T.
    Org Lett; 2014 Apr 04; 16(7):1976-9. PubMed ID: 24660822
    [Abstract] [Full Text] [Related]

  • 19. Gymnothelignans A-O: conformation and absolute configuration analyses of lignans bearing tetrahydrofuran from Gymnotheca chinensis.
    He D, Ding L, Xu H, Lei X, Xiao H, Zhou Y.
    J Org Chem; 2012 Oct 05; 77(19):8435-43. PubMed ID: 22946788
    [Abstract] [Full Text] [Related]

  • 20. Asymmetric synthesis of (+)-galbelgin, (-)-kadangustin J, (-)-cyclogalgravin and (-)-pycnanthulignenes A and B, three structurally distinct lignan classes, using a common chiral precursor.
    Rye CE, Barker D.
    J Org Chem; 2011 Aug 19; 76(16):6636-48. PubMed ID: 21749139
    [Abstract] [Full Text] [Related]

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