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

PUBMED FOR HANDHELDS

Journal Abstract Search

197 related items for PubMed ID: 18283687

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. CuBr for KA(2) reaction: en route to propargylic amines bearing a quaternary carbon center.
    Tang X, Kuang J, Ma S.
    Chem Commun (Camb); 2013 Oct 11; 49(79):8976-8. PubMed ID: 23962962
    [Abstract] [Full Text] [Related]

  • 28. Organocatalytic asymmetric synthesis of propargylamines with two adjacent stereocenters: mannich-type reactions of in situ generated C-alkynyl imines with β-keto esters.
    Kano T, Yurino T, Maruoka K.
    Angew Chem Int Ed Engl; 2013 Oct 25; 52(44):11509-12. PubMed ID: 24038946
    [Abstract] [Full Text] [Related]

  • 29. Gold-catalyzed highly enantioselective synthesis of axially chiral allenes.
    Lo VK, Wong MK, Che CM.
    Org Lett; 2008 Feb 07; 10(3):517-9. PubMed ID: 18181641
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Chemoselective amination of propargylic C(sp³)-H bonds by cobalt(II)-based metalloradical catalysis.
    Lu H, Li C, Jiang H, Lizardi CL, Zhang XP.
    Angew Chem Int Ed Engl; 2014 Jul 01; 53(27):7028-32. PubMed ID: 24840605
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Enantioselective intramolecular propargylic amination using chiral copper-pybox complexes as catalysts.
    Shibata M, Nakajima K, Nishibayashi Y.
    Chem Commun (Camb); 2014 Jul 25; 50(58):7874-7. PubMed ID: 24911134
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Chemoselective C-H bond activation: ligand and solvent free iron-catalyzed oxidative C-C cross-coupling of tertiary amines with terminal alkynes. Reaction scope and mechanism.
    Volla CM, Vogel P.
    Org Lett; 2009 Apr 16; 11(8):1701-4. PubMed ID: 19296636
    [Abstract] [Full Text] [Related]

  • 37. Diastereo- and enantioselective propargylation of benzofuranones catalyzed by pybox-copper complex.
    Zhao L, Huang G, Guo B, Xu L, Chen J, Cao W, Zhao G, Wu X.
    Org Lett; 2014 Nov 07; 16(21):5584-7. PubMed ID: 25325792
    [Abstract] [Full Text] [Related]

  • 38. A highly efficient and selective Au(I)-catalyzed tandem synthesis of diversely substituted pyrrolo[1,2-a]quinolines in aqueous media.
    Liu XY, Che CM.
    Angew Chem Int Ed Engl; 2008 Nov 07; 47(20):3805-10. PubMed ID: 18399561
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Synthesis of tertiary propargylamines via a rationally designed multicomponent reaction of primary amines, formaldehyde, arylboronic acids and alkynes.
    Wang J, Shen Q, Li P, Peng Y, Song G.
    Org Biomol Chem; 2014 Aug 14; 12(30):5597-600. PubMed ID: 24969221
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.