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


1250 related items for PubMed ID: 17497798

  • 1. Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates.
    Davis FA, Song M.
    Org Lett; 2007 Jun 07; 9(12):2413-6. PubMed ID: 17497798
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Asymmetric synthesis of beta-amino carbonyl compounds with N-sulfinyl beta-amino Weinreb amides.
    Davis FA, Nolt MB, Wu Y, Prasad KR, Li D, Yang B, Bowen K, Lee SH, Eardley JH.
    J Org Chem; 2005 Mar 18; 70(6):2184-90. PubMed ID: 15760203
    [Abstract] [Full Text] [Related]

  • 4. Asymmetric synthesis of cyclic cis-beta-amino acid derivatives using sulfinimines and prochiral Weinreb amide enolates.
    Davis FA, Theddu N.
    J Org Chem; 2010 Jun 04; 75(11):3814-20. PubMed ID: 20462208
    [Abstract] [Full Text] [Related]

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

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

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Asymmetric synthesis of alpha-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline.
    Davis FA, Ramachandar T, Liu H.
    Org Lett; 2004 Sep 16; 6(19):3393-5. PubMed ID: 15355060
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.
    Ooi T, Takeuchi M, Kato D, Uematsu Y, Tayama E, Sakai D, Maruoka K.
    J Am Chem Soc; 2005 Apr 13; 127(14):5073-83. PubMed ID: 15810842
    [Abstract] [Full Text] [Related]

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

  • 12. Total synthesis of (5R,6R,8R,9S)-(-)-5,9Z-indolizidine 221T using sulfinimine-derived N-sulfinyl beta-amino ketones.
    Davis FA, Song M, Qiu H, Chai J.
    Org Biomol Chem; 2009 Dec 21; 7(24):5067-73. PubMed ID: 20024099
    [Abstract] [Full Text] [Related]

  • 13. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines.
    Lin GQ, Xu MH, Zhong YW, Sun XW.
    Acc Chem Res; 2008 Jul 21; 41(7):831-40. PubMed ID: 18533688
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Nucleophilic perfluoroalkylation of imines and carbonyls: perfluoroalkyl sulfones as efficient perfluoroalkyl-transfer motifs.
    Prakash GK, Wang Y, Mogi R, Hu J, Mathew T, Olah GA.
    Org Lett; 2010 Jul 02; 12(13):2932-5. PubMed ID: 20518520
    [Abstract] [Full Text] [Related]

  • 16. Asymmetric synthesis of cyclic alpha-amino phosphonates using masked oxo sulfinimines (N-sulfinyl imines).
    Davis FA, Lee SH, Xu H.
    J Org Chem; 2004 May 28; 69(11):3774-81. PubMed ID: 15153008
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Asymmetric synthesis of aziridine 2-phosphonates from enantiopure sulfinimines (N-sulfinyl imines). Synthesis of alpha-amino phosphonates.
    Davis FA, Wu Y, Yan H, McCoull W, Prasad KR.
    J Org Chem; 2003 Mar 21; 68(6):2410-9. PubMed ID: 12636410
    [Abstract] [Full Text] [Related]

  • 19. Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines.
    Callebaut G, Mangelinckx S, Kiss L, Sillanpää R, Fülöp F, De Kimpe N.
    Org Biomol Chem; 2012 Mar 21; 10(11):2326-38. PubMed ID: 22311107
    [Abstract] [Full Text] [Related]

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


    Page: [Next] [New Search]
    of 63.