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Journal Abstract Search

583 related items for PubMed ID: 19537726

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  • 2. Efficient synthesis of α-tertiary α-silylamines from aryl sulfonylimidates via one-pot, sequential C-Si/C-C bond formations.
    Han XJ, Yao M, Lu CD.
    Org Lett; 2012 Jun 01; 14(11):2906-9. PubMed ID: 22621235
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  • 5. Stereoselective and diversity-oriented synthesis of trisubstituted allylic alcohols and amines.
    Schmidt Y, Breit B.
    Chemistry; 2011 Oct 10; 17(42):11789-96. PubMed ID: 21898610
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  • 9. Addition of indolyl and pyrrolyl grignard reagents to 1-acylpyridinium salts.
    Kuethe JT, Comins DL.
    J Org Chem; 2004 Apr 16; 69(8):2863-6. PubMed ID: 15074941
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  • 10. Generation and tandem reactions of 1-alkenyl-1,1-heterobimetallics: practical and versatile reagents for organic synthesis.
    Li H, Carroll PJ, Walsh PJ.
    J Am Chem Soc; 2008 Mar 19; 130(11):3521-31. PubMed ID: 18302376
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  • 11. Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates.
    Manoso AS, Ahn C, Soheili A, Handy CJ, Correia R, Seganish WM, Deshong P.
    J Org Chem; 2004 Nov 26; 69(24):8305-14. PubMed ID: 15549801
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  • 12. Complete regioselective addition of grignard reagents to pyrazine N-oxides, toward an efficient enantioselective synthesis of substituted piperazines.
    Andersson H, Banchelin TS, Das S, Gustafsson M, Olsson R, Almqvist F.
    Org Lett; 2010 Jan 15; 12(2):284-6. PubMed ID: 20000607
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  • 13. Catalytic enantioselective addition of dialkylzinc to N-diphenylphosphinoylimines. A practical synthesis of alpha-chiral amines.
    Boezio AA, Charette AB.
    J Am Chem Soc; 2003 Feb 19; 125(7):1692-3. PubMed ID: 12580582
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  • 15. New general method for regio- and stereoselective allylic substitution with aryl and alkenyl coppers derived from Grignard reagents.
    Kiyotsuka Y, Katayama Y, Acharya HP, Hyodo T, Kobayashi Y.
    J Org Chem; 2009 Mar 06; 74(5):1939-51. PubMed ID: 19199795
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  • 16. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).
    Terao J, Kambe N.
    Acc Chem Res; 2008 Nov 18; 41(11):1545-54. PubMed ID: 18973349
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  • 17. An efficient method to convert lactams and amides into 2,2-dialkylated amines.
    Agosti A, Britto S, Renaud P.
    Org Lett; 2008 Apr 03; 10(7):1417-20. PubMed ID: 18314998
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  • 18. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted enones. Construction of all-carbon quaternary chiral centers.
    Martin D, Kehrli S, d'Augustin M, Clavier H, Mauduit M, Alexakis A.
    J Am Chem Soc; 2006 Jul 05; 128(26):8416-7. PubMed ID: 16802804
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  • 19. CpIr complex-catalyzed N-heterocyclization of primary amines with diols: a new catalytic system for environmentally benign synthesis of cyclic amines.
    Fujita K, Fujii T, Yamaguchi R.
    Org Lett; 2004 Sep 30; 6(20):3525-8. PubMed ID: 15387539
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  • 20. Transition-metal-free electrophilic amination between aryl Grignard reagents and N-chloroamines.
    Hatakeyama T, Yoshimoto Y, Ghorai SK, Nakamura M.
    Org Lett; 2010 Apr 02; 12(7):1516-9. PubMed ID: 20222741
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