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721 related items for PubMed ID: 16117531

  • 1. A highly efficient and direct approach for synthesis of enantiopure beta-amino alcohols by reductive cross-coupling of chiral N-tert-butanesulfinyl imines with aldehydes.
    Zhong YW, Dong YZ, Fang K, Izumi K, Xu MH, Lin GQ.
    J Am Chem Soc; 2005 Aug 31; 127(34):11956-7. PubMed ID: 16117531
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  • 3. Highly efficient asymmetric synthesis of vinylic amino alcohols by Zn-promoted benzoyloxyallylation of chiral N-tert-butanesulfinyl imines: facile and rapid access to (-)-cytoxazone.
    Liu M, Sun XW, Xu MH, Lin GQ.
    Chemistry; 2009 Oct 05; 15(39):10217-24. PubMed ID: 19711382
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  • 9. Asymmetric copper-catalyzed synthesis of alpha-amino boronate esters from N-tert-butanesulfinyl aldimines.
    Beenen MA, An C, Ellman JA.
    J Am Chem Soc; 2008 Jun 04; 130(22):6910-1. PubMed ID: 18461938
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  • 10. Practical asymmetric synthesis of alpha-branched 2-piperazinylbenzylamines by 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines.
    Jiang W, Chen C, Marinkovic D, Tran JA, Chen CW, Arellano LM, White NS, Tucci FC.
    J Org Chem; 2005 Oct 28; 70(22):8924-31. PubMed ID: 16238329
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  • 11. SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
    Wang B, Wang YJ.
    Org Lett; 2009 Aug 06; 11(15):3410-3. PubMed ID: 19603761
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  • 12. Synthesis and applications of tert-butanesulfinamide.
    Robak MT, Herbage MA, Ellman JA.
    Chem Rev; 2010 Jun 09; 110(6):3600-740. PubMed ID: 20420386
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  • 13. Asymmetric synthesis of protected 1,2-amino alcohols using tert-butanesulfinyl aldimines and ketimines.
    Tang TP, Volkman SK, Ellman JA.
    J Org Chem; 2001 Dec 28; 66(26):8772-8. PubMed ID: 11749605
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  • 18. Asymmetric Rh(I)-catalyzed addition of MIDA boronates to N-tert-butanesulfinyl aldimines: development and comparison to trifluoroborates.
    Brak K, Ellman JA.
    J Org Chem; 2010 May 07; 75(9):3147-50. PubMed ID: 20387846
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  • 19. Enantiopure trifluoromethylated β(3,3)-amino acids: synthesis by asymmetric Reformatsky reaction with stable analogues of trifluoromethyl N-tert-butanesulfinylketoimines and incorporation into α/β-peptides.
    Grellepois F.
    J Org Chem; 2013 Feb 01; 78(3):1127-37. PubMed ID: 23273379
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