Large-scale manufacture of peptide therapeutics by chemical synthesis von Bray, Brian L

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Process Development of TRI-999, a Fatty-Acid-Modified HIV Fusion Inhibitory Peptide von Zhang, Huyi, Schneider, Stephen E, Bray, Brian L, Friedrich, Paul E, Tvermoes, Nicolai A, Mader, Catherine J, Whight, Sheila R, Niemi, Toivo E, Silinski, Peter, Picking, Tony, Warren, Marquitta, Wring, Stephen A

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Development of HIV fusion inhibitors von Schneider, Stephen E., Bray, Brian L., Mader, Catherine J., Friedrich, Paul E., Anderson, Mark W., Taylor, Tracy S., Boshernitzan, Natalia, Niemi, Toivo E., Fulcher, Brian C., Whight, Sheila R., White, Jonathan M., Greene, Reagan J., Stoltenberg, Larry E., Lichty, Maynard

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N-(Triisopropylsilyl)pyrrole. A progenitor "par excellence" of 3-substituted pyrroles von Bray, Brian L, Mathies, Peter H, Naef, Reto, Solas, Dennis R, Tidwell, Thomas T, Artis, Dean R, Muchowski, Joseph M

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Synthesis of (.+-.)-catharanthine, (+)-anhydrovinblastine, and (-)-anhydrovincovaline von Raucher, Stanley, Bray, Brian L, Lawrence, Ross F

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Oxidative radical cyclization to pyrroles under reducing conditions. Reductive desulfonylation of α-sulfonylpyrroles with tri-n-butyltin hydride von Antonio, Yulia, De La Cruz, Ma. Elizabeth, Galeazzi, Edvige, Guzman, Angel, Bray, Brian L, Greenhouse, Robert, Kurz, Lilia J, Lustig, David A, Maddox, Michael L, Muchowski, Joseph M

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Improved procedures for the preparation of (+) - (1R, 2S, 4R)-4-amino-2-hydroxy-1-hydroxymethyl cyclopentane von Bray, Brian L., Dolan, Simon C., Halter, Bernard, Lackey, J.William, Schilling, Mark B., Tapolczay, David J.

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A convenient procedure for the preparation of ethoxyacetylene and ethoxyethynyl carbinols von Raucher, Stanley, Bray, Brian L

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Synthesis of acylpyrroles via .alpha.-(dimethylamino)-.alpha.-pyrrolylacetonitriles von Bray, Brian L, Muchowski, Joseph M

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Total synthesis of (.+-.)-catharanthine von Raucher, Stanley, Bray, Brian L

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Innovation: Large-scale manufacture of peptide therapeutics by chemical synthesis von Bray, Brian L

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Synthesis of 5-substituted pyrrole-2-carboxaldehydes. Part I. Generation of formal 5-lithiopyrrole-2-carboxaldehyde equivalents by bromine-lithium exchange of 2-bromo-6-(diisopropy... von Berthiaume, Sylvie L, Bray, Brian L, Hess, Petr, Liu, Yanzhou, Maddox, Michael L, Muchowski, Joseph M, Scheller, Markus E

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α-(Dialkylamino)-α-pyrrolylacetonitriles. A potpourri of useful synthetic transformations von Bray, Brian L, Muchowski, Joseph M

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Innovation: Large-Scale Manufacture of Peptide Therapeutics by Chemical Synthesis von Bray, Brian L.

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HIV FUSION INHIBITOR PEPTIDES WITH IMPROVED BIOLOGICAL PROPERTIES von BRAY, BRIAN L, FRIEDRICH, PAUL E, SCHNEIDER, STEPHEN E, ZHANG, HUYI, DWYER, JOHN, JOHNSTON, BARBARA E, TVERMOES, NICOLAI A

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PRODUCTION METHOD OF PHENYL GUANIDINE SALTS AND THEIR INTERMEDIATES von KANG, MYUNGOL, SCHNEIDER, STEPHEN, JOHNSON, MICHAEL, ROSS, BRAY, BRIAN, L

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Lithiated Azafulvenes by Halogen/Metal Interchange of Brominated 6-(Diisopropylamino)-1-azafulvene Derivatives. Novel synthesis of 5-mono- and 4,5-disubstituted 1H-pyrrole-2-carbal... von Bray, Brian L., Hess, Petr, Muchowski, Joseph M., Scheller, Markus E.

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HIV-fusionsinhibitorpeptider med forbedrede biologiske egenskaber von JOHNSTON, BARBARA, E, ZHANG, HUYI, TVERMOES, NICOLAI, A, DWYER, JOHN, BRAY, BRIAN, L, FRIEDRICH, PAUL, E, SCHNEIDER, STEPHEN, E

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HIV FUSION INHIBITOR PEPTIDES WITH IMPROVED BIOLOGICAL PROPERTIES von NICOLAI A. TVERMOES, HUYI ZHANG, STEPHEN E. SCHNEIDER, PAUL E. FRIEDRICH, JOHN DWYER, BRIAN L. BRAY, BARBARA E. JOHNSTON

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HIV FUSION INHIBITOR PEPTIDES WITH IMPROVED BIOLOGICAL PROPERTIES von FRIEDRICH PAUL E, ZHANG HUYI, TVERMOES NICOLAI A, SCHNEIDER STEPHEN E, JOHNSTON BARBARA E, DWYER JOHN J, BRAY BRIAN L

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