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Journal Abstract Search

334 related items for PubMed ID: 15787529

  • 1. 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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  • 2. Nitrile biotransformations for highly efficient and enantioselective syntheses of electrophilic oxiranecarboxamides.
    Wang MX, Lin SJ, Liu CS, Zheng QY, Li JS.
    J Org Chem; 2003 May 30; 68(11):4570-3. PubMed ID: 12762774
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  • 3. 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
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  • 4. Nitrile biotransformation for highly enantioselective synthesis of 3-substituted 2,2-dimethylcyclopropanecarboxylic acids and amides.
    Wang MX, Feng GQ.
    J Org Chem; 2003 Jan 24; 68(2):621-4. PubMed ID: 12530896
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  • 5. An unusual beta-vinyl effect leading to high efficiency and enantioselectivity of the amidase, nitrile biotransformations for the preparation of enantiopure 3-arylpent-4-enoic acids and amides and their applications in synthesis.
    Gao M, Wang DX, Zheng QY, Wang MX.
    J Org Chem; 2006 Dec 08; 71(25):9532-5. PubMed ID: 17137391
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  • 6. 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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  • 7. Nitrile biotransformations for the synthesis of highly enantioenriched beta-hydroxy and beta-amino acid and amide derivatives: a general and simple but powerful and efficient benzyl protection strategy to increase enantioselectivity of the amidase.
    Ma DY, Wang DX, Pan J, Huang ZT, Wang MX.
    J Org Chem; 2008 Jun 06; 73(11):4087-91. PubMed ID: 18459810
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  • 9. Highly efficient and enantioselective biotransformations of racemic azetidine-2-carbonitriles and their synthetic applications.
    Leng DH, Wang DX, Pan J, Huang ZT, Wang MX.
    J Org Chem; 2009 Aug 21; 74(16):6077-82. PubMed ID: 19627128
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  • 10. Remarkable electronic and steric effects in the nitrile biotransformations for the preparation of enantiopure functionalized carboxylic acids and amides: implication for an unsaturated carbon-carbon bond binding domain of the amidase.
    Gao M, Wang DX, Zheng QY, Huang ZT, Wang MX.
    J Org Chem; 2007 Aug 03; 72(16):6060-6. PubMed ID: 17604398
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  • 15. Characterisation of nitrilase and nitrile hydratase biocatalytic systems.
    Brady D, Beeton A, Zeevaart J, Kgaje C, van Rantwijk F, Sheldon RA.
    Appl Microbiol Biotechnol; 2004 Mar 03; 64(1):76-85. PubMed ID: 14666389
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  • 16. Regioselective ring opening of amino epoxides with nitriles: an easy synthesis of (2R,3S)- and (2S,3S)-1,3-diaminoalkan-2-ols with differently protected amine functions.
    Concellón JM, Suárez JR, Del Solar V.
    J Org Chem; 2005 Sep 02; 70(18):7447-50. PubMed ID: 16122275
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  • 19. Purification and characterization of the enantioselective nitrile hydratase from Rhodococcus sp. AJ270.
    Song L, Wang M, Yang X, Qian S.
    Biotechnol J; 2007 Jun 02; 2(6):717-24. PubMed ID: 17330219
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