Search Results - "Seenaiah, Mallikanti"

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  1. 1

    Palladium Mediated Rapid Deprotection of N‑Terminal Cysteine under Native Chemical Ligation Conditions for the Efficient Preparation of Synthetically Challenging Proteins by Jbara, Muhammad, Maity, Suman Kumar, Seenaiah, Mallikanti, Brik, Ashraf

    Published in Journal of the American Chemical Society (20-04-2016)
    “…Facilitating the process of chemical protein synthesis is an important goal in order to enable the efficient preparation of large and novel protein analogues…”
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    Journal Article
  2. 2

    Convergent Versus Sequential Protein Synthesis: The Case of Ubiquitinated and Glycosylated H2B by Seenaiah, Mallikanti, Jbara, Muhammad, Mali, Sachitanand M., Brik, Ashraf

    Published in Angewandte Chemie International Edition (12-10-2015)
    “…The chemical synthesis of a protein from four fragments or more applying native chemical ligation could be achieved stepwise, in one‐pot, convergently, or on a…”
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    Journal Article
  3. 3

    Solid phase chemical ligation employing a rink amide linker for the synthesis of histone H2B protein by Jbara, Muhammad, Seenaiah, Mallikanti, Brik, Ashraf

    “…Presented here is a solid phase chemical ligation strategy employing native chemical ligation and the commercially available Rink-amide linker as a key element…”
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    Journal Article
  4. 4

    Convergent Versus Sequential Protein Synthesis: The Case of Ubiquitinated and Glycosylated H2B by Seenaiah, Mallikanti, Jbara, Muhammad, Mali, Sachitanand M., Brik, Ashraf

    Published in Angewandte Chemie (12-10-2015)
    “…The chemical synthesis of a protein from four fragments or more applying native chemical ligation could be achieved stepwise, in one‐pot, convergently, or on a…”
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    Journal Article
  5. 5

    Dehydroalanine-Based Diubiquitin Activity Probes by Haj-Yahya, Najat, Hemantha, Hosahalli P, Meledin, Roman, Bondalapati, Somasekhar, Seenaiah, Mallikanti, Brik, Ashraf

    Published in Organic letters (17-01-2014)
    “…A strategy for the synthesis of dehydroalanine based diubiquitin activity probes is described. The site-specific introduction of dehydroalanine was achieved…”
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  6. 6

    Intramolecular copper(I)-catalyzed 1,3-dipolar cycloaddition of azido-alkynes: synthesis of triazolo-benzoxazepine derivatives and their biological evaluation by Chandrasekhar, Srivari, Seenaiah, Mallikanti, Kumar, Abhishek, Reddy, Chada Raji, Mamidyala, Suman Kumar, Kumar, Chityal Ganesh, Balasubramanian, Sridhar

    Published in Tetrahedron letters (16-02-2011)
    “…Synthesis of a series of [1,2,3] triazolo [5,1- c] [1,4]benzoxazepine derivatives have been accomplished by the intramolecular Cu(I)-catalyzed cycloaddition of…”
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    Journal Article
  7. 7

    Formation of Periodic γ-Turns in α/β-Hybrid Peptides: DFT and NMR Experimental Evidence by Chandrasekhar, Srivari, Rao, Kakita Veera Mohana, Seenaiah, Mallikanti, Naresh, Police, Devi, Ambure Sharada, Jagadeesh, Bharatam

    Published in Chemistry, an Asian journal (01-02-2014)
    “…Hybrid peptidic oligomers comprising natural and unnatural amino acid residues that can exhibit biomolecular folding and hydrogen‐bonding mimicry have…”
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  8. 8

    Formation of Periodic [gamma]-Turns in [alpha]/[beta]-Hybrid Peptides: DFT and NMR Experimental Evidence by Chandrasekhar, Srivari, Rao, Kakita Veera Mohana, Seenaiah, Mallikanti, Naresh, Police, Devi, Ambure Sharada, Jagadeesh, Bharatam

    Published in Chemistry, an Asian journal (01-02-2014)
    “…Hybrid peptidic oligomers comprising natural and unnatural amino acid residues that can exhibit biomolecular folding and hydrogen-bonding mimicry have…”
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    Journal Article
  9. 9

    Total Synthesis of Azumamide E and Sugar Amino Acid-Containing Analogue by Chandrasekhar, Srivari, Rao, Chennamaneni Lohitha, Seenaiah, Mallikanti, Naresh, Police, Jagadeesh, Bharatam, Manjeera, Dharani, Sarkar, Arpita, Bhadra, Manika Pal

    Published in Journal of organic chemistry (02-01-2009)
    “…An efficient and practical total synthesis of marine cyclic tetrapeptide, natural product azumamide E (1) is achieved via high-yielding reactions. The strategy…”
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    Journal Article