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Information Journal Paper

Title

PEPTIDE-CATALYSIS IN ASYMMETRIC ORGANIC SYNTHESIS

Pages

  89-98

Abstract

 Stereo-selectivity is an important feature in the development of the synthesis of biologically active organic compounds. In this process, (bio) catalysts exhibit substrate specificity that allows high levels of chemo- and regio-selectivity. Over the past decade, several PEPTIDEs have been developed as effective bio-catalysts for a range of synthetically valuable reactions. In comparison with proteins owing a large number of amino acids and high molecular weights, PEPTIDE-catalysts possess only a few amino acid residues, which may adopt a secondary structure suitable for synthesis of desired chiral products. In addition, the flexible nature of PEPTIDEs consents for tuning of reactivity and selectivity by replacing amino acid residues. These unique aspects provide attractive biocatalysts platform for asymmetric syntheses.

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    • Cite

    APA: Copy

    MOGHARABI, MEHDI, REZAEI, SHAHLA, & FARAMARZI, MOHAMMAD ALI. (2017). PEPTIDE-CATALYSIS IN ASYMMETRIC ORGANIC SYNTHESIS. TRENDS IN PEPTIDE AND PROTEIN SCIENES, 1(3), 89-98. SID. https://sid.ir/paper/350773/en

    Vancouver: Copy

    MOGHARABI MEHDI, REZAEI SHAHLA, FARAMARZI MOHAMMAD ALI. PEPTIDE-CATALYSIS IN ASYMMETRIC ORGANIC SYNTHESIS. TRENDS IN PEPTIDE AND PROTEIN SCIENES[Internet]. 2017;1(3):89-98. Available from: https://sid.ir/paper/350773/en

    IEEE: Copy

    MEHDI MOGHARABI, SHAHLA REZAEI, and MOHAMMAD ALI FARAMARZI, “PEPTIDE-CATALYSIS IN ASYMMETRIC ORGANIC SYNTHESIS,” TRENDS IN PEPTIDE AND PROTEIN SCIENES, vol. 1, no. 3, pp. 89–98, 2017, [Online]. Available: https://sid.ir/paper/350773/en

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