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Journal Abstract Search

160 related items for PubMed ID: 20812732

  • 1. Enantiopure trans-3-arylaziridine-2-carboxamides: preparation by bacterial hydrolysis and ring-openings toward enantiopure, unnatural D-α-amino acids.
    Morán-Ramallal R, Liz R, Gotor V.
    J Org Chem; 2010 Oct 01; 75(19):6614-24. PubMed ID: 20812732
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  • 3. Nitrile biotransformations for the efficient synthesis of highly enantiopure 1-arylaziridine-2-carboxylic acid derivatives and their stereoselective ring-opening reactions.
    Wang JY, Wang DX, Zheng QY, Huang ZT, Wang MX.
    J Org Chem; 2007 Mar 16; 72(6):2040-5. PubMed ID: 17286438
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  • 5. Practical synthesis of optically active alpha,alpha-disubstituted malonamic acids through asymmetric hydrolysis of malonamide derivatives with Rhodococcus sp. CGMCC 0497.
    Wu ZL, Li ZY.
    J Org Chem; 2003 Mar 21; 68(6):2479-82. PubMed ID: 12636421
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  • 6. Regioselective and stereospecific synthesis of enantiopure 1,3-oxazolidin-2-ones by intramolecular ring opening of 2-(Boc-aminomethyl)aziridines. Preparation of the antibiotic linezolid.
    Morán-Ramallal R, Liz R, Gotor V.
    Org Lett; 2008 May 15; 10(10):1935-8. PubMed ID: 18433140
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  • 8. High kinetic resolution in the addition of a racemic allenylzinc onto enantiopure N-tert-butanesulfinimines: concise synthesis of enantiopure trans-2-ethynylaziridines.
    Chemla F, Ferreira F.
    J Org Chem; 2004 Nov 26; 69(24):8244-50. PubMed ID: 15549794
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  • 9. Lipase-catalyzed resolution of (2R*,3S*)- and (2R*,3R*)-3-methyl-3-phenyl-2-aziridinemethanol at low temperatures and determination of the absolute configurations of the four stereoisomers.
    Sakai T, Liu Y, Ohta H, Korenaga T, Ema T.
    J Org Chem; 2005 Feb 18; 70(4):1369-75. PubMed ID: 15704972
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  • 11. 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
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  • 12. The first direct enzymatic hydrolysis of alicyclic beta-amino esters: a route to enantiopure cis and trans beta-amino acids.
    Forró E, Fülöp F.
    Chemistry; 2007 Nov 11; 13(22):6397-401. PubMed ID: 17492820
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  • 13. Enantiopure α-Trifluoromethylated Aziridine-2-carboxylic Acid (α-TfmAzy): Synthesis and Peptide Coupling.
    Ouerfelli O, Simon J, Chelain E, Pytkowicz J, Besbes R, Brigaud T.
    Org Lett; 2020 Apr 17; 22(8):2946-2949. PubMed ID: 32216364
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  • 16. Enantioselective formal synthesis of (-)-podophyllotoxin from (2S,3R)-3-arylaziridine-2-carboxylate.
    Takahashi M, Suzuki N, Ishikawa T.
    J Org Chem; 2013 Apr 05; 78(7):3250-61. PubMed ID: 23496308
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  • 17. Nitrile biotransformations for highly enantioselective synthesis of oxiranecarboxamides with tertiary and quaternary stereocenters; efficient chemoenzymatic approaches to enantiopure alpha-methylated serine and isoserine derivatives.
    Wang MX, Deng G, Wang DX, Zheng QY.
    J Org Chem; 2005 Apr 01; 70(7):2439-44. PubMed ID: 15787529
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  • 20. Asymmetric synthesis of aziridine 2-phosphonates from enantiopure sulfinimines (N-sulfinyl imines). Synthesis of alpha-amino phosphonates.
    Davis FA, Wu Y, Yan H, McCoull W, Prasad KR.
    J Org Chem; 2003 Mar 21; 68(6):2410-9. PubMed ID: 12636410
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