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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

391 related articles for article (PubMed ID: 11841277)

  • 1. Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis.
    Austin JF; MacMillan DW
    J Am Chem Soc; 2002 Feb; 124(7):1172-3. PubMed ID: 11841277
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Organocatalytic asymmetric Friedel-Crafts alkylation of indoles with simple alpha,beta-unsaturated ketones.
    Bartoli G; Bosco M; Carlone A; Pesciaioli F; Sambri L; Melchiorre P
    Org Lett; 2007 Mar; 9(7):1403-5. PubMed ID: 17346059
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Organocatalytic enantioselective indole alkylations of alpha,beta-unsaturated ketones.
    Chen W; Du W; Yue L; Li R; Wu Y; Ding LS; Chen YC
    Org Biomol Chem; 2007 Mar; 5(5):816-21. PubMed ID: 17315068
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The enantioselective organocatalytic 1,4-addition of electron-rich benzenes to alpha,beta-unsaturated aldehydes.
    Paras NA; MacMillan DW
    J Am Chem Soc; 2002 Jul; 124(27):7894-5. PubMed ID: 12095321
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The first enantioselective organocatalytic Mukaiyama-Michael reaction: a direct method for the synthesis of enantioenriched gamma-butenolide architecture.
    Brown SP; Goodwin NC; MacMillan DW
    J Am Chem Soc; 2003 Feb; 125(5):1192-4. PubMed ID: 12553821
    [TBL] [Abstract][Full Text] [Related]  

  • 6. High-pressure accelerated asymmetric organocatalytic Friedel-Crafts alkylation of indoles with enones: application to quaternary stereogenic centers construction.
    Łyżwa D; Dudziński K; Kwiatkowski P
    Org Lett; 2012 Mar; 14(6):1540-3. PubMed ID: 22397622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles.
    Dou X; Yao W; Jiang C; Lu Y
    Chem Commun (Camb); 2014 Oct; 50(77):11354-7. PubMed ID: 25163647
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enantioselective organocatalytic cyclopropanations. The identification of a new class of iminium catalyst based upon directed electrostatic activation.
    Kunz RK; MacMillan DW
    J Am Chem Soc; 2005 Mar; 127(10):3240-1. PubMed ID: 15755116
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enantioselective organo-cascade catalysis.
    Huang Y; Walji AM; Larsen CH; MacMillan DW
    J Am Chem Soc; 2005 Nov; 127(43):15051-3. PubMed ID: 16248643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B.
    Austin JF; Kim SG; Sinz CJ; Xiao WJ; MacMillan DW
    Proc Natl Acad Sci U S A; 2004 Apr; 101(15):5482-7. PubMed ID: 15067109
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Asymmetric organocatalytic N-alkylation of indole-2-carbaldehydes with alpha,beta-unsaturated aldehydes: one-pot synthesis of chiral pyrrolo[1,2-a]indole-2-carbaldehydes.
    Hong L; Sun W; Liu C; Wang L; Wang R
    Chemistry; 2010 Jan; 16(2):440-4. PubMed ID: 19938023
    [No Abstract]   [Full Text] [Related]  

  • 12. Metal-free, mild, nonepimerizing, chemo- and enantio- or diastereoselective N-alkylation of amines by alcohols via oxidation/imine-iminium formation/reductive amination: a pragmatic synthesis of octahydropyrazinopyridoindoles and higher ring analogues.
    Khan IA; Saxena AK
    J Org Chem; 2013 Dec; 78(23):11656-69. PubMed ID: 23988233
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enantioselective synthesis of a highly potent selective serotonin reuptake inhibitor. An application of imidazolidinone catalysis to the alkylation of indoles with an alpha,beta-disubstituted alpha,beta-unsaturated aldehyde.
    King HD; Meng Z; Denhart D; Mattson R; Kimura R; Wu D; Gao Q; Macor JE
    Org Lett; 2005 Aug; 7(16):3437-40. PubMed ID: 16048311
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enantioselective organocatalytic amine conjugate addition.
    Chen YK; Yoshida M; MacMillan DW
    J Am Chem Soc; 2006 Jul; 128(29):9328-9. PubMed ID: 16848457
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CuH-Catalyzed Enantioselective Alkylation of Indole Derivatives with Ligand-Controlled Regiodivergence.
    Ye Y; Kim ST; Jeong J; Baik MH; Buchwald SL
    J Am Chem Soc; 2019 Mar; 141(9):3901-3909. PubMed ID: 30696242
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The versatile roles of ammonium salt catalysts in enantioselective reduction and alkylation of α,β-unsaturated aldehydes: iminium catalysis, enamine catalysis and acid catalysis.
    Xiang SK; Zhang B; Zhang LH; Cui Y; Jiao N
    Chem Commun (Camb); 2011 May; 47(17):5007-9. PubMed ID: 21424018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Organocatalytic stereoselective mannich reaction of 3-substituted oxindoles.
    Tian X; Jiang K; Peng J; Du W; Chen YC
    Org Lett; 2008 Aug; 10(16):3583-6. PubMed ID: 18642826
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Enantioselective organocatalytic alpha-fluorination of aldehydes.
    Beeson TD; Macmillan DW
    J Am Chem Soc; 2005 Jun; 127(24):8826-8. PubMed ID: 15954790
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Enantioselective Friedel-Crafts alkylation for synthesis of 2-substituted indole derivatives.
    Zhang Y; Liu X; Zhao X; Zhang J; Zhou L; Lin L; Feng X
    Chem Commun (Camb); 2013 Dec; 49(96):11311-3. PubMed ID: 24158312
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Organocatalytic enantioselective Friedel-Crafts alkylation of 4,7-dihydroindoles with alpha,beta-unsaturated aldehydes: an easy access to 2-substituted indoles.
    Hong L; Liu C; Sun W; Wang L; Wong K; Wang R
    Org Lett; 2009 May; 11(10):2177-80. PubMed ID: 19385607
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.