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Journal Abstract Search

212 related items for PubMed ID: 22217094

  • 1. Diastereoselective preparation of (R)- and (S)-2-methoxy-2-phenylpent-3-ynoic acids and their use as reliable chiral derivatizing agents.
    Pérez-Estrada S, Joseph-Nathan P, Jiménez-Vázquez HA, Medina-López ME, Ayala-Mata F, Zepeda LG.
    J Org Chem; 2012 Feb 17; 77(4):1640-52. PubMed ID: 22217094
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  • 3. Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy.
    Porto S, Seco JM, Espinosa JF, Quiñoá E, Riguera R.
    J Org Chem; 2008 Aug 01; 73(15):5714-22. PubMed ID: 18582122
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  • 4. NMR determinations of the absolute configuration of alpha-chiral primary amines.
    Fukui H, Fukushi Y.
    Org Lett; 2010 Jun 18; 12(12):2856-9. PubMed ID: 20462201
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  • 8. Confirmation by IR of the preferred conformations of CFTA esters in solution: a highly reliable criterion for the stereochemistry assignment of chiral alcohols.
    Omata K, Kotani K, Kabuto K, Fujiwara T, Takeuchi Y.
    Chem Commun (Camb); 2010 May 28; 46(20):3610-2. PubMed ID: 20393658
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  • 10. (1-Naphthyl)(trifluoromethyl) O-carboxy anhydride as a chiral derivatizing agent: eclipsed conformation enforced by hydrogen bonding.
    Thillaye du Boullay O, Alba A, Oukhatar F, Martin-Vaca B, Bourissou D.
    Org Lett; 2008 Oct 16; 10(20):4669-72. PubMed ID: 18816122
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  • 11. Relative and absolute stereochemistry of secondary/secondary diols: low-temperature 1H NMR of their bis-MPA esters.
    Freire F, Calderón F, Seco JM, Fernandez-Mayoralas A, Quiñoá E, Riguera R.
    J Org Chem; 2007 Mar 30; 72(7):2297-301. PubMed ID: 17343414
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  • 13. Three-component chiral derivatizing protocols for NMR spectroscopic enantiodiscrimination of hydroxy acids and primary amines.
    Chaudhari SR, Suryaprakash N.
    J Org Chem; 2012 Jan 06; 77(1):648-51. PubMed ID: 22145800
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  • 18. C-2/c-3 annulation and C-2 alkylation of indoles with 2-alkoxycyclopropanoate esters.
    Bajtos B, Yu M, Zhao H, Pagenkopf BL.
    J Am Chem Soc; 2007 Aug 08; 129(31):9631-4. PubMed ID: 17630734
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