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995 related items for PubMed ID: 17973389

  • 1. 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]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
    Kelley BT, Joullié MM.
    Org Lett; 2010 Oct 01; 12(19):4244-7. PubMed ID: 20812750
    [Abstract] [Full Text] [Related]

  • 4. Solvent- and temperature-dependent functionalisation of enantioenriched aziridines.
    de Ceglie MC, Musio B, Affortunato F, Moliterni A, Altomare A, Florio S, Luisi R.
    Chemistry; 2011 Jan 03; 17(1):286-96. PubMed ID: 21207624
    [Abstract] [Full Text] [Related]

  • 5. Selective ring-opening of nonactivated amino aziridines by thiols and unusual nucleophilic substitution of a dibenzylamino group.
    Concellón JM, Bernad PL, Suárez JR, García-Granda S, Díaz MR.
    J Org Chem; 2005 Nov 11; 70(23):9411-6. PubMed ID: 16268615
    [Abstract] [Full Text] [Related]

  • 6. Enantioselective syntheses of morpholines and their homologues via S(N)2-type ring opening of aziridines and azetidines with haloalcohols.
    Ghorai MK, Shukla D, Das K.
    J Org Chem; 2009 Sep 18; 74(18):7013-22. PubMed ID: 19673479
    [Abstract] [Full Text] [Related]

  • 7. Nitrile and amide biotransformations for the synthesis of enantiomerically pure 3-arylaziridine-2-carboxamide derivatives and their stereospecific ring-opening reactions.
    Wang JY, Wang DX, Pan J, Huang ZT, Wang MX.
    J Org Chem; 2007 Nov 23; 72(24):9391-4. PubMed ID: 17958451
    [Abstract] [Full Text] [Related]

  • 8. Organolithium-induced alkylative ring opening of aziridines: synthesis of unsaturated amino alcohols and ethers.
    Hodgson DM, Stefane B, Miles TJ, Witherington J.
    J Org Chem; 2006 Oct 27; 71(22):8510-5. PubMed ID: 17064027
    [Abstract] [Full Text] [Related]

  • 9. Regioselective and Stereodivergent Synthesis of Enantiomerically Pure Vic-Diamines from Chiral β-Amino Alcohols with 2-Pyridyl and 6-(2,2'-Bipyridyl) Moieties.
    Wosińska-Hrydczuk M, Boratyński PJ, Skarżewski J.
    Molecules; 2020 Feb 07; 25(3):. PubMed ID: 32046110
    [Abstract] [Full Text] [Related]

  • 10. Ring opening of a resin-bound chiral aziridine with phenol nucleophiles.
    Ottesen LK, Jaroszewski JW, Franzyk H.
    J Org Chem; 2010 Aug 06; 75(15):4983-91. PubMed ID: 20617832
    [Abstract] [Full Text] [Related]

  • 11. Nucleophilic ring-opening of epoxide and aziridine acetates for the stereodivergent synthesis of β-hydroxy and β-amino γ-lactams.
    Bisol TB, Bortoluzzi AJ, Sá MM.
    J Org Chem; 2011 Feb 04; 76(3):948-62. PubMed ID: 21194209
    [Abstract] [Full Text] [Related]

  • 12. Selective synthesis of cis- and trans-2-(methyl/phenyl)-3-(trifluoromethyl)aziridines and their regio- and stereospecific ring opening.
    Moens M, De Kimpe N, D'hooghe M.
    J Org Chem; 2014 Jun 20; 79(12):5558-68. PubMed ID: 24845942
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 14. BF3 x OEt2-mediated highly regioselective S(N)2-type ring-opening of N-activated aziridines and N-activated azetidines by tetraalkylammonium halides.
    Ghorai MK, Kumar A, Tiwari DP.
    J Org Chem; 2010 Jan 01; 75(1):137-51. PubMed ID: 19968243
    [Abstract] [Full Text] [Related]

  • 15. Mild metal-free syn-stereoselective ring opening of activated epoxides and aziridines with aryl borates.
    Pineschi M, Bertolini F, Haak RM, Crotti P, Macchia F.
    Chem Commun (Camb); 2005 Mar 21; (11):1426-8. PubMed ID: 15756325
    [Abstract] [Full Text] [Related]

  • 16. On the utility of S-mesitylsulfinimines for the stereoselective synthesis of chiral amines and aziridines.
    Roe C, Moragas Solá T, Sasraku-Neequaye L, Hobbs H, Churcher I, MacPherson D, Stockman RA.
    Chem Commun (Camb); 2011 Jul 14; 47(26):7491-3. PubMed ID: 21629906
    [Abstract] [Full Text] [Related]

  • 17. Tandem sequence of cross metathesis--ring-closing metathesis reaction of alkynyl silyloxy-tethered enynes.
    Park S, Kim M, Lee D.
    J Am Chem Soc; 2005 Jul 06; 127(26):9410-5. PubMed ID: 15984868
    [Abstract] [Full Text] [Related]

  • 18. Addition of TMS-substituted oxiranyl anions to acylsilanes. A highly stereoselective approach to tetrasubstituted (Z)-β-hydroxy-α-TMS silyl enol ethers.
    Song Z, Kui L, Sun X, Li L.
    Org Lett; 2011 Mar 18; 13(6):1440-3. PubMed ID: 21341723
    [Abstract] [Full Text] [Related]

  • 19. Synthetic stitching with silicon: geminal alkylation-hydroxylation of alkynyl carbonyl compounds.
    Trost BM, Ball ZT.
    J Am Chem Soc; 2004 Nov 03; 126(43):13942-4. PubMed ID: 15506753
    [Abstract] [Full Text] [Related]

  • 20. Stereoselective syntheses of 4-oxa diaminopimelic acid and its protected derivatives via aziridine ring opening.
    Liu H, Pattabiraman VR, Vederas JC.
    Org Lett; 2007 Oct 11; 9(21):4211-4. PubMed ID: 17850092
    [Abstract] [Full Text] [Related]

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