These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


209 related items for PubMed ID: 15858648

  • 1. 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]

  • 2. 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 07; 71(9):2248-55. PubMed ID: 17827688
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Syntheses and antimicrobial activity of tetrasubstituted tetrahydrofuran lignan stereoisomers.
    Nakato T, Yamauchi S, Tago R, Akiyama K, Maruyama M, Sugahara T, Kishida T, Koba Y.
    Biosci Biotechnol Biochem; 2009 Jul 07; 73(7):1608-17. PubMed ID: 19584535
    [Abstract] [Full Text] [Related]

  • 8. Stereocontrolled assembly of tetrasubstituted tetrahydrofurans: a concise synthesis of virgatusin.
    Akindele T, Marsden SP, Cumming JG.
    Org Lett; 2005 Aug 18; 7(17):3685-8. PubMed ID: 16092850
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. A versatile stereoselective synthesis of endo,exo-furofuranones: application to the enantioselective synthesis of furofuran lignans.
    Swain NA, Brown RC, Bruton G.
    J Org Chem; 2004 Jan 09; 69(1):122-9. PubMed ID: 14703387
    [Abstract] [Full Text] [Related]

  • 14. Radical carboxyarylation approach to lignans. Total synthesis of (-)-arctigenin, (-)-matairesinol, and related natural products.
    Fischer J, Reynolds AJ, Sharp LA, Sherburn MS.
    Org Lett; 2004 Apr 29; 6(9):1345-8. PubMed ID: 15101738
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 65(1):29-34. PubMed ID: 11272842
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 67(4):838-46. PubMed ID: 12784626
    [Abstract] [Full Text] [Related]

  • 18. Application of enantioselective radical reactions: synthesis of (+)-ricciocarpins A and B.
    Sibi MP, He L.
    Org Lett; 2004 May 27; 6(11):1749-52. PubMed ID: 15151405
    [Abstract] [Full Text] [Related]

  • 19. Enantioselective synthesis of (-)-wikstromol using a new approach via malic acid.
    Sefkow M.
    J Org Chem; 2001 Apr 06; 66(7):2343-9. PubMed ID: 11281774
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 11.