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192 related items for PubMed ID: 29308468

  • 1. 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]

  • 2. A bio-inspired total synthesis of tetrahydrofuran lignans.
    Albertson AK, Lumb JP.
    Angew Chem Int Ed Engl; 2015 Feb 09; 54(7):2204-8. PubMed ID: 25582827
    [Abstract] [Full Text] [Related]

  • 3. Stereoselective synthesis of tetrahydrofuran lignans via BF(3) x OEt(2)-promoted reductive deoxygenation/epimerization of cyclic hemiketal: synthesis of (-)-odoratisol C, (-)-futokadsurin A, (-)-veraguensin, (+)-fragransin A(2), (+)-galbelgin, and (+)-talaumidin.
    Kim H, Wooten CM, Park Y, Hong J.
    Org Lett; 2007 Sep 27; 9(20):3965-8. PubMed ID: 17764190
    [Abstract] [Full Text] [Related]

  • 4. Arylnaphthalene lignans through Pd-Catalyzed [2+2+2] cocyclization of arynes and diynes: total synthesis of Taiwanins C and E.
    Sato Y, Tamura T, Mori M.
    Angew Chem Int Ed Engl; 2004 Apr 26; 43(18):2436-40. PubMed ID: 15114584
    [No Abstract] [Full Text] [Related]

  • 5. Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.
    Nakato T, Yamauchi S.
    J Nat Prod; 2007 Oct 26; 70(10):1588-92. PubMed ID: 17887723
    [Abstract] [Full Text] [Related]

  • 6. Total synthesis of (±)-sacidumlignans D and A through Ueno-Stork radical cyclization reaction.
    Zhang JJ, Yan CS, Peng Y, Luo ZB, Xu XB, Wang YW.
    Org Biomol Chem; 2013 Apr 21; 11(15):2498-513. PubMed ID: 23440075
    [Abstract] [Full Text] [Related]

  • 7. Redox-triggered C-C coupling of diols and alkynes: synthesis of β,γ-unsaturated α-hydroxyketones and furans by ruthenium-catalyzed hydrohydroxyalkylation.
    McInturff EL, Nguyen KD, Krische MJ.
    Angew Chem Int Ed Engl; 2014 Mar 17; 53(12):3232-5. PubMed ID: 24677357
    [Abstract] [Full Text] [Related]

  • 8. Tetrahydrofuran lignans via tandem oxidative anionic-radical processes or reductive radical cyclizations.
    Jahn U, Rudakov D.
    Org Lett; 2006 Sep 28; 8(20):4481-4. PubMed ID: 16986930
    [Abstract] [Full Text] [Related]

  • 9. Total synthesis of (-)-talaumidin and (-)-galbelgin.
    Xue P, Wang LP, Jiao XZ, Jiang YJ, Xiao Q, Luo ZG, Xie P, Liang XT.
    J Asian Nat Prod Res; 2009 Sep 28; 11(3):281-7. PubMed ID: 19408154
    [Abstract] [Full Text] [Related]

  • 10. Tandem Olefin Metathesis/Oxidative Cyclization: Synthesis of Tetrahydrofuran Diols from Simple Olefins.
    Dornan PK, Lee D, Grubbs RH.
    J Am Chem Soc; 2016 May 25; 138(20):6372-5. PubMed ID: 27133576
    [Abstract] [Full Text] [Related]

  • 11. Total synthesis of cis-solamin: exploiting the RuO4-catalyzed oxidative cyclization of dienes.
    Göksel H, Stark CB.
    Org Lett; 2006 Aug 03; 8(16):3433-6. PubMed ID: 16869628
    [Abstract] [Full Text] [Related]

  • 12. Improved procedure for the enantiometric synthesis of 1-hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicycl.
    Ishibashi F, Hayashita M, Okazaki M, Shuto Y.
    Biosci Biotechnol Biochem; 2001 Jan 03; 65(1):29-34. PubMed ID: 11272842
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Bioinspired total synthesis of gymnothelignan N.
    Li H, Zhang Y, Xie X, Ma H, Zhao C, Zhao G, She X.
    Org Lett; 2014 Sep 05; 16(17):4440-3. PubMed ID: 25103476
    [Abstract] [Full Text] [Related]

  • 15. Acetal-initiated Prins bicyclization for the synthesis of hexahydrofuro-[3,4-c]furan lignans and octahydropyrano[3,4-c]pyran derivatives.
    Reddy BV, Ramana Reddy M, Sridhar B, Singarapu KK.
    Org Biomol Chem; 2014 Jul 14; 12(26):4754-62. PubMed ID: 24875046
    [Abstract] [Full Text] [Related]

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  • 17. 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]

  • 18. 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 21; 71(9):2248-55. PubMed ID: 17827688
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