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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 19904925

  • 1. An unexpected highly stereoselective bisaziridination of (E,E)-1,4-dialkyl-2,3-dinitrobutadienes followed by a nitro group driven ring enlargement.
    Ciogli A, Fioravanti S, Gasparrini F, Pellacani L, Rizzato E, Spinelli D, Tardella PA.
    J Org Chem; 2009 Dec 18; 74(24):9314-8. PubMed ID: 19904925
    [Abstract] [Full Text] [Related]

  • 2. NaI-catalyzed highly regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines: highly stereoselective synthesis of cis-vinylic aziridines.
    Ma S, Zhang J, Lu L, Jin X, Cai Y, Hou H.
    Chem Commun (Camb); 2005 Feb 21; (7):909-11. PubMed ID: 15700078
    [Abstract] [Full Text] [Related]

  • 3. Enantioselective aza-Henry reactions of cyclic α-carbonyl ketimines under bifunctional catalysis.
    Parra A, Alfaro R, Marzo L, Moreno-Carrasco A, García Ruano JL, Alemán J.
    Chem Commun (Camb); 2012 Oct 09; 48(78):9759-61. PubMed ID: 22918139
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  • 4. A regio- and stereoselective approach to quaternary centers from chiral trisubstituted aziridines.
    Forbeck EM, Evans CD, Gilleran JA, Li P, Joullié MM.
    J Am Chem Soc; 2007 Nov 21; 129(46):14463-9. PubMed ID: 17973389
    [Abstract] [Full Text] [Related]

  • 5. Trisubstituted aziridine ring-opening by phenol derivatives: stereo- and regioselective formation of chiral tertiary alkyl-aryl ethers.
    Li P, Forbeck EM, Evans CD, Joullié MM.
    Org Lett; 2006 Oct 26; 8(22):5105-7. PubMed ID: 17048854
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  • 6. One-pot enantioselective syntheses of iminosugar derivatives using organocatalytic anti-michael-anti-aza-Henry reactions.
    Imashiro R, Uehara H, Barbas CF.
    Org Lett; 2010 Nov 19; 12(22):5250-3. PubMed ID: 21033702
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  • 8. Simple cyclohexanediamine-derived primary amine thiourea catalyzed highly enantioselective conjugate addition of nitroalkanes to enones.
    Mei K, Jin M, Zhang S, Li P, Liu W, Chen X, Xue F, Duan W, Wang W.
    Org Lett; 2009 Jul 02; 11(13):2864-7. PubMed ID: 19485350
    [Abstract] [Full Text] [Related]

  • 9. Chemistry of tetrathiomolybdate: aziridine ring opening reactions and facile synthesis of interesting sulfur heterocycles.
    Sureshkumar D, Koutha SM, Chandrasekaran S.
    J Am Chem Soc; 2005 Sep 21; 127(37):12760-1. PubMed ID: 16159244
    [Abstract] [Full Text] [Related]

  • 10. Cycloaddition/Ring opening reaction sequences of N-alkenyl aziridines: influence of the aziridine nitrogen on stereoselectivity.
    Siebert MR, Yudin AK, Tantillo DJ.
    Org Lett; 2008 Jan 03; 10(1):57-60. PubMed ID: 18052185
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  • 13. Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-beta-lactams and study of their ring opening.
    D'hooghe M, Mollet K, Dekeukeleire S, De Kimpe N.
    Org Biomol Chem; 2010 Feb 07; 8(3):607-15. PubMed ID: 20090977
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  • 15. Regioselective synthesis of fluoroalkylated beta-aminophosphorus derivatives and aziridines from phosphorylated oximes and nucleophilic reagents.
    Palacios F, Ochoa de Retana AM, Alonso JM.
    J Org Chem; 2006 Aug 04; 71(16):6141-8. PubMed ID: 16872198
    [Abstract] [Full Text] [Related]

  • 16. Stereoselective synthesis of highly functionalized nitrocyclopropanes via organocatalyic conjugate addition to nitroalkenes.
    McCooey SH, McCabe T, Connon SJ.
    J Org Chem; 2006 Sep 15; 71(19):7494-7. PubMed ID: 16958552
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  • 17. Epi-cinchona based thiourea organocatalyst family as an efficient asymmetric Michael addition promoter: enantioselective conjugate addition of nitroalkanes to chalcones and alpha,beta-unsaturated N-acylpyrroles.
    Vakulya B, Varga S, Soós T.
    J Org Chem; 2008 May 02; 73(9):3475-80. PubMed ID: 18376862
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  • 19. Asymmetric meso-aziridine ring-opening reactions using a chiral zirconium catalyst.
    Seki K, Yu R, Yamazaki Y, Yamashita Y, Kobayashi S.
    Chem Commun (Camb); 2009 Oct 14; (38):5722-4. PubMed ID: 19774248
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  • 20. A highly efficient and general method for the ring-opening of aziridines with various nucleophiles in DMSO.
    Wu J, Sun X, Sun W.
    Org Biomol Chem; 2006 Nov 21; 4(22):4231-5. PubMed ID: 17312980
    [Abstract] [Full Text] [Related]


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