Search Results - "Massa, Mark A."

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    Systematic Investigation of EDC/sNHS-Mediated Bioconjugation Reactions for Carboxylated Peptide Substrates by Totaro, Kyle A, Liao, Xiaoli, Bhattacharya, Keshab, Finneman, Jari I, Sperry, Justin B, Massa, Mark A, Thorn, Jennifer, Ho, Sa V, Pentelute, Bradley L

    Published in Bioconjugate chemistry (20-04-2016)
    “…1-Ethyl-3-(3-(dimethylamino)­propyl)­carbodiimide (EDC) bioconjugations have been utilized in preparing variants for medical research. While there have been…”
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    Journal Article
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    Effects of Conformational Changes in Peptide–CRM197 Conjugate Vaccines by Jaffe, Jake, Wucherer, Kristin, Sperry, Justin, Zou, Qin, Chang, Qing, Massa, Mark A, Bhattacharya, Keshab, Kumar, Sandeep, Caparon, Maire, Stead, David, Wright, Paul, Dirksen, Anouk, Francis, Matthew B

    Published in Bioconjugate chemistry (16-01-2019)
    “…Conjugate vaccines prepared with the cross-reactive material 197 (CRM197) carrier protein have been successful in the clinic and are of great interest in the…”
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    Effects of Conformational Changes in Peptide-CRM 197 Conjugate Vaccines by Jaffe, Jake, Wucherer, Kristin, Sperry, Justin, Zou, Qin, Chang, Qing, Massa, Mark A, Bhattacharya, Keshab, Kumar, Sandeep, Caparon, Maire, Stead, David, Wright, Paul, Dirksen, Anouk, Francis, Matthew B

    Published in Bioconjugate chemistry (16-01-2019)
    “…Conjugate vaccines prepared with the cross-reactive material 197 (CRM ) carrier protein have been successful in the clinic and are of great interest in the…”
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    Functionalization of Cp4Fe4(CO)4:  Contrasts and Comparisons with Ferrocene by Westmeyer, Mark D, Massa, Mark A, Rauchfuss, Thomas B, Wilson, Scott R

    Published in Journal of the American Chemical Society (14-01-1998)
    “…Thermolysis of a xylene solution of Cp2Fe2(CO)4 and PPh3 yields primarily Cp4Fe4(CO)4 (1) together with smaller amounts of (C5H4Ph)Cp3Fe4(CO)4 and…”
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    The total synthesis of the natural product endothelin converting enzyme (ECE) inhibitor, WS75624 B by Patt, William C., Massa, Mark A.

    Published in Tetrahedron letters (24-02-1997)
    “…The first total synthesis of WS75624 B, 1, an endothelin converting enzyme inhibitor produced in a fermentation broth of Saccharothrix sp. No. 75624 is…”
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    Effects of Conformational Changes in Peptide–CRM^sub 197^ Conjugate Vaccines by Jaffe, Jake, Wucherer, Kristin, Sperry, Justin, Zou, Qin, Chang, Qing, Massa, Mark A, Bhattacharya, Keshab, Kumar, Sandeep, Caparon, Maire, Stead, David, Wright, Paul, Dirksen, Anouk, Francis, Matthew B

    Published in Bioconjugate chemistry (16-01-2019)
    “…Conjugate vaccines prepared with the cross-reactive material 197 (CRM197) carrier protein have been successful in the clinic and are of great interest in the…”
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    Journal Article
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    Butenolide Endothelin Antagonists with Improved Aqueous Solubility by Patt, William C, Cheng, Xue-Min, Repine, Joseph T, Lee, Chet, Reisdorph, Bill R, Massa, Mark A, Doherty, Annette M, Welch, Kathleen M, Bryant, John W, Flynn, Michael A, Walker, Donnelle M, Schroeder, Richard L, Haleen, Stephen J, Keiser, Joan A

    Published in Journal of medicinal chemistry (17-06-1999)
    “…Continued development around our ETA-selective endothelin (ET) antagonist 1 (CI-1020) has led to the synthesis of analogues with improved aqueous solubility…”
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    3-Methyl-4 H-[1,2,4]-oxadiazol-5-one: a versatile synthon for protecting monosubstituted acetamidines by Moormann, Alan E., Wang, Jane L., Palmquist, Katherine E., Promo, Michele A., Snyder, Jeffery S., Scholten, Jeffrey A., Massa, Mark A., Sikorski, James A., Webber, R. Keith

    Published in Tetrahedron (2004)
    “…The utilization of 3-methyl-4 H-[1,2,4]-oxadiazol-5-one as a versatile protected acetamidine is demonstrated through employment in a variety of synthetic…”
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    Synthesis of novel substituted pyridines as inhibitors of endothelin coverting enzyme-1 (ECE-1) by Massa, Mark A., Patt, William C., Ahn, Kyunghye, Sisneros, Andre M., Herman, Sarah B., Doherty, Annette

    Published in Bioorganic & medicinal chemistry letters (01-08-1998)
    “…A series of bi-aryl pyridine carboxylic acids has been prepared and evaluated as inhibitors of ECE-1. The analogs were prepared by Pd catalyzed cross couplings…”
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