Additives Promote Noyori-type Reductions of a β‑Keto-γ-lactam: Asymmetric Syntheses of Serotonin Norepinephrine Reuptake Inhibitors von Magnus, Nicholas A, Astleford, Bret A, Laird, Dana L. T, Maloney, Todd D, McFarland, Adam D, Rizzo, John R, Ruble, J. Craig, Stephenson, Gregory A, Wepsiec, James P

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Practical Asymmetric Synthesis of an Edivoxetine·HCl Intermediate via an Efficient Diazotization Process von Kopach, Michael E, Heath, Perry C, Scherer, Roger B, Pietz, Mark A, Astleford, Bret A, McCauley, Mary Kay, Singh, Utpal K, Wong, Sze Wing, Coppert, David M, Kerr, Mark S, Houghton, Peter G, Rhodes, Gary A, Tharp, Gregg A

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Syntheses of a Selective Peroxisome Proliferator Activated Receptor Modulator and Practical New Preparations of 2-(4-Alkoxyphenyl)ethylamines von Magnus, Nicholas A, Astleford, Bret A, Brennan, John, Stout, James R, Tharp-Taylor, Roger W

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Synthesis of 1-alkyl-1,2,4-triazoles: a new one-pot regiospecific procedure von Astleford, Bret A, Goe, Gerald L, Keay, James G, Scriven, Eric F. V

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Resolution of δ-Lactams Provides Access to Nonracemic Benzoquinolinones:  The Synthesis of LY300502 and LY300503 von Astleford, Bret A, Audia, James E, Deeter, Jack, Heath, Perry C, Janisse, Samantha K, Kress, Thomas J, Wepsiec, James P, Weigel, Leland O

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Studies on the phosphorylation of LY303366 von Udodong, Uko E., Turner, William W., Astleford, Bret A., Brown, Frank, Clayton, Marcella T., Dunlap, Steven E., Frank, Scott A., Grutsch, John L., LaGrandeur, Lisa M., Verral, Daniel E., Werner, John A.

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Selective methylphosphonylation of an echinocandin B analog derived from LY303366 von Udodong, Uko E, Hansen, Marvin M, Verral, Daniel E, Harkness, Allen R, Grutsch, John L, Miller, William D, Astleford, Bret

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Scope of phthalimido chemistry I. Extension of utility by conversion to the opcb protecting group von Astleford, Bret, Weigel, Leland O.

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VERFAHREN ZUR HERSTELLUNG VON 10, 11METHANODIBENZOSUBERANDERIVATEN von WILSON, THOMAS, MICHAEL, KOBIERSKI, MICHAEL, EDWARD, ASTLEFORD, BRET, ANTHONY, BARNETT, CHARLES, JACKSON

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PROCESS FOR PREPARING A 10,11-METHANODIBENZOSUBERANE DERIVATIVE von WILSON, THOMAS, MICHAEL, KOBIERSKI, MICHAEL, EDWARD, ASTLEFORD, BRET, ANTHONY, BARNETT, CHARLES, JACKSON

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Process for preparing a 10,11-methanodibenzosuberane derivative von BARNETT CHARLES JACKSON, KOBIERSKI MICHAEL EDWARD, WILSON THOMAS MICHAEL, ASTLEFORD BRET ANTHONY

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Process for preparing a 10,11-methanodibenzosuberane derivative von Astleford, Bret Anthony, Barnett, Charles Jackson, Kobierski, Michael Edward, Wilson, Thomas Michael

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Process for preparing a 10,11-methanodibenzosuberane derivative von Astleford, Bret Anthony, Barnett, Charles Jackson, Kobierski, Michael Edward, Wilson, Thomas Michael

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Process for preparing a 10,11-methanodibenzosuberane derivative von BARNETT CHARLES JACKSON, KOBIERSKI MICHAEL EDWARD, WILSON THOMAS MICHAEL, ASTLEFORD BRET ANTHONY

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PROCESS FOR PREPARING A 10,11-METHANODIBENZOSUBERANE DERIVATIVE von WILSON, THOMAS, MICHAEL, KOBIERSKI, MICHAEL, EDWARD, ASTLEFORD, BRET, ANTHONY, BARNETT, CHARLES, JACKSON

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Process for preparing a 10,11-methanodibenzosuberane derivative von THOMAS MICHAEL WILSON, BRET ANTHONY ASTLEFORD, CHARLES JACKSON BARNETT, MICHAEL EDWARD KOBIERSKI

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PROCESS FOR PREPARING A 10,11-METHANODIBENZOSUBERANE DERIVATIVE von WILSON, THOMAS, MICHAEL, KOBIERSKI, MICHAEL, EDWARD, ASTLEFORD, BRET, ANTHONY, BARNETT, CHARLES, JACKSON

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PROCESS FOR PREPARING A 10,11-METHANODIBENZOSUBERANE DERIVATIVE von WILSON, THOMAS MICHAEL, ASTLEFORD, BRET ANTHONY, KOBIERSKI, MICHAEL EDWARD, BARNETT, CHARLES JACKSON

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PROCEDIMIENTO DE PREPARACION DE UN DERIVADO DE 10,11-METANODIBENZOSUBERANO von WILSON, THOMAS, MICHAEL, KOBIERSKI, MICHAEL, EDWARD, ASTLEFORD, BRET, ANTHONY, BARNETT, CHARLES, JACKSON

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PROCEDIMIENTO PARA PREPARAR UN DERIVADO DE 10,11-METANODIBENZOSUBERANO von BARNETT CHARLES JACKSON, KOBIERSKI MICHAEL EDWARD, WILSON THOMAS MICHAEL, ASTLEFORD BRET ANTHONY

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