Search Results - "RUSSELL RONALD K" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Process Development for Scale-Up of a Novel 3,5-Substituted Thiazolidine-2,4-dione Compound as a Potent Inhibitor for Estrogen-Related Receptor 1

Process Development for Scale-Up of a Novel 3,5-Substituted Thiazolidine-2,4-dione Compound as a Potent Inhibitor for Estrogen-Related Receptor 1

by Li, Xun, Russell, Ronald K, Spink, Jan, Ballentine, Scott, Teleha, Christopher, Branum, Shawn, Wells, Kenneth, Beauchamp, Derek, Patch, Raymond, Huang, Hui, Player, Mark, Murray, William
Published in Organic process research & development (21.02.2014)

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Lab-Scale Preparation of a Novel Cyclopenta[b]furan Chemokine Receptor Antagonist

Lab-Scale Preparation of a Novel Cyclopenta[b]furan Chemokine Receptor Antagonist

by Teleha, Christopher A, Branum, Shawn, Zhang, Yongzheng, Reuman, Michael E, Van Der Steen, Luc, Verbeek, Marc, Fawzy, Nagy, Leo, Gregory C, Winters, Michael P, Kang, Fu-An, Kolpak, Michael, Beauchamp, Derek A, Lanter, James C, Russell, Ronald K, Sui, Zhihua, Vanbaelen, Hilde
Published in Organic process research & development (19.12.2014)

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Lab-Scale Preparation of a Novel Carbocyclic Chemokine Receptor Antagonist

Lab-Scale Preparation of a Novel Carbocyclic Chemokine Receptor Antagonist

by Teleha, Christopher A, Branum, Shawn, Zhang, Yongzheng, Reuman, Michael E, Van Der Steen, Luc, Verbeek, Marc, Fawzy, Nagy, Leo, Gregory C, Kang, Fu-An, Cai, Chaozhong, Kolpak, Michael, Beauchamp, Derek A, Wall, Mark J, Russell, Ronald K, Sui, Zhihua, Vanbaelen, Hilde
Published in Organic process research & development (19.12.2014)

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Synthesis of Mavatrep: A Potent Antagonist of Transient Receptor Potential Vanilloid‑1

Synthesis of Mavatrep: A Potent Antagonist of Transient Receptor Potential Vanilloid‑1

by Wells, Kenneth M, Mehrman, Steven J, Abdel-Magid, Ahmed F, Ferraro, Caterina, Scott, Lorraine, Zhong, Hua Marlon, Teleha, Christopher A, Ballentine, Scott, Li, Xun, Russell, Ronald K, Spink, Jan M, Diamond, Craig, Youells, Scott, Zhang, Yongzheng, Tsay, Fuh-Rong, Cesco-Cancia, Sergio, Manzo, Stephen M, Beauchamp, Derek A
Published in Organic process research & development (20.11.2015)

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An Efficient Synthesis of 3‑Substituted N‑Glycoside Indoles Useful as Sodium-Dependent Glucose Transporter Inhibitors

An Efficient Synthesis of 3‑Substituted N‑Glycoside Indoles Useful as Sodium-Dependent Glucose Transporter Inhibitors

by Li, Xun, Wells, Kenneth M, Branum, Shawn, Damon, Sandra, Youells, Scott, Beauchamp, Derek A, Palmer, David, Stefanick, Stephen, Russell, Ronald K, Murray, William
Published in Organic process research & development (16.11.2012)

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Crystallization of a Cephalosporin and an ERR-1: Assembly of an Inexpensive Crystallization Platform

Crystallization of a Cephalosporin and an ERR-1: Assembly of an Inexpensive Crystallization Platform

by Wells, Kenneth M, Beauchamp, Derek A, Fermier, Adam, Wu, Wenju, Mehrman, Steven, Youells, Scott, Hu, Zhiyong, Li, Xun, Macielag, Mark J, Bignan, Gilles, Xu, Guozhang, Zhao, Bao-Ping, Huang, Lian, Weber, James, Gaul, Micheal D, Russell, Ronald K
Published in Crystal growth & design (06.11.2013)

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Using Potassium Carbonate to Scavenge Hydrogen Fluoride: A Scale-Up Process for Quantitative Production of (1-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-(oxo-κO)-3-quinolinecarboxylato-κO3)difluoro−Boron

Using Potassium Carbonate to Scavenge Hydrogen Fluoride: A Scale-Up Process for Quantitative Production of (1-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-(oxo-κO)-3-quinolinecarboxylato-κO3)difluoro−Boron

by Li, Xun, Russell, Ronald K
Published in Organic process research & development (16.05.2008)

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An Efficient Synthetic Process for Scale-Up Production of 4,5-Diamino-2-(trifluoromethyl)benzonitrile and 5-Bromo-3-(trifluoromethyl)benzene-1,2-diamine

An Efficient Synthetic Process for Scale-Up Production of 4,5-Diamino-2-(trifluoromethyl)benzonitrile and 5-Bromo-3-(trifluoromethyl)benzene-1,2-diamine

by Li, Xun, Ng, Raymond A, Zhang, Yongzheng, Russell, Ronald K, Sui, Zhihua
Published in Organic process research & development (15.05.2009)

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Scalable Synthesis of the VEGF-R2 Kinase Inhibitor JNJ-17029259 Using Ultrasound-Mediated Addition of MeLi−CeCl3 to a Nitrile

Scalable Synthesis of the VEGF-R2 Kinase Inhibitor JNJ-17029259 Using Ultrasound-Mediated Addition of MeLi−CeCl3 to a Nitrile

by Reuman, Michael, Beish, Sandra, Davis, Jeremy, Batchelor, Mark J, Hutchings, Martin C, Moffat, David F. C, Connolly, Peter J, Russell, Ronald K
Published in Journal of organic chemistry (01.02.2008)

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Regio- and diastereoselective ring-opening of (S)-(−)-2-(trifluoromethyl)oxirane with chiral 2,5-disubstituted tetrahydroquinolines in hexafluoro-2-propanol

Regio- and diastereoselective ring-opening of (S)-(−)-2-(trifluoromethyl)oxirane with chiral 2,5-disubstituted tetrahydroquinolines in hexafluoro-2-propanol

by Li, Xun, Russell, Ronald K, Chen, Hongfeng, Zhang, Yongzheng, Ballentine, Scott, Spink, Jan, Branum, Shawn, Liu, Fuqiang, Chen, Yanping, Rammeloo, Thomas, Aelterman, Wim, Sorgi, Kirk L, Murray, William V
Published in Green chemistry : an international journal and green chemistry resource : GC (01.01.2010)

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Synthesis of a 5-((Aryloxy)methyl)-3-(4-(trifluoromethyl)phenyl)[1,2,4]thiadiazole Derivative: A Promising PPARα,δ Agonist

Synthesis of a 5-((Aryloxy)methyl)-3-(4-(trifluoromethyl)phenyl)[1,2,4]thiadiazole Derivative: A Promising PPARα,δ Agonist

by Reuman, Michael, Hu, Zhiyong, Kuo, Gee-Hong, Li, Xun, Russell, Ronald K, Shen, Lan, Youells, Scott, Zhang, Yongzheng
Published in Organic process research & development (01.11.2007)

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Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 3. Development of an Acid-Catalyzed Racemization Process for (S)-2,8-(Dimethoxy)-5-{4-[2-(1-piperidinyl)ethoxy]phenyl}−11,12-dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta[1,2-a]naphthalene

Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 3. Development of an Acid-Catalyzed Racemization Process for (S)-2,8-(Dimethoxy)-5-{4-[2-(1-piperidinyl)ethoxy]phenyl}−11,12-dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta[1,2-a]naphthalene

by Li, Xun, Russell, Ronald K, Horváth, András, Jain, Nareshkumar, Depré, Dominique, Ormerod, Dominic, Aelterman, Wim, Sui, Zhihua
Published in Organic process research & development (16.01.2009)

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Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up Of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives

Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up Of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives

by Li, Xun, Reuman, Michael, Russell, Ronald K, Youells, Scott, Beish, Sandra, Hu, Zhiyong, Branum, Shawn, Jain, Nareshkumar, Sui, Zhihua
Published in Organic process research & development (01.07.2007)

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Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 1. Process Development for Scale-up of 2,5,8-Substituted 5,11-Dihydrochromeno[4,3-c]chromene Derivatives

Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 1. Process Development for Scale-up of 2,5,8-Substituted 5,11-Dihydrochromeno[4,3-c]chromene Derivatives

by Li, Xun, Reuman, Michael, Russell, Ronald K, Adams, Richard, Ma, Robert, Branum, Shawn, Youells, Scott, Roberts, Jerry, Jain, Nareshkumar, Kanojia, Ramesh, Sui, Zhihua
Published in Organic process research & development (01.05.2007)

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Development of a Scalable Synthetic Process for Selective Bromination of 4-Methyl-3,7-Substituted Coumarins

Development of a Scalable Synthetic Process for Selective Bromination of 4-Methyl-3,7-Substituted Coumarins

by Li, Xun, Jain, Nareshkumar, Russell, Ronald K, Ma, Robert, Branum, Shawn, Xu, Jiayi, Sui, Zhihua
Published in Organic process research & development (01.03.2006)

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Substituted Salicylanilides as Inhibitors of Two-Component Regulatory Systems in Bacteria

Substituted Salicylanilides as Inhibitors of Two-Component Regulatory Systems in Bacteria

by Macielag, Mark J, Demers, James P, Fraga-Spano, Stephanie A, Hlasta, Dennis J, Johnson, Sigmond G, Kanojia, Ramesh M, Russell, Ronald K, Sui, Zhihua, Weidner-Wells, Michele A, Werblood, Harvey, Foleno, Barbara D, Goldschmidt, Raul M, Loeloff, Michael J, Webb, Glenda C, Barrett, John F
Published in Journal of medicinal chemistry (30.07.1998)

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β-Alkylthio indolyl carbinols: Potent nonsteroidal antiandrogens with oral efficacy in a prostate cancer model

β-Alkylthio indolyl carbinols: Potent nonsteroidal antiandrogens with oral efficacy in a prostate cancer model

by Lanter, James C., Fiordeliso, James J., Alford, Vernon C., Zhang, Xuqing, Wells, Kenneth M., Russell, Ronald K., Allan, George F., Lai, Muh-Tsann, Linton, Olivia, Lundeen, Scott, Sui, Zhihua
Published in Bioorganic & medicinal chemistry letters (01.05.2007)

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Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives

Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives

by Li, Xun, Reuman, Michael, Russell, Ronald K, Youells, Scott, Beish, Sandra, Hu, Zhiyong, Branum, Shawn, Jain, Nareshkumar, Sui, Zhihua
Published in Organic process research & development (18.01.2008)

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Direct conversion of substituted pyrrole-2-carboxylic acid methyl esters to their 2-carbonitrile analogues

Direct conversion of substituted pyrrole-2-carboxylic acid methyl esters to their 2-carbonitrile analogues

by Li, Xun, Reurnan, Michael, Russell, Ronald K.
Published in Heterocycles (31.12.2006)

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An Efficient Process for Synthesis of 3-(R)-3-(2,3-Dihydrobenzofuran-5-yl)- 1,2,3,4-tetrahydropyrrolo[3,4-b]quinolin-9-one

An Efficient Process for Synthesis of 3-(R)-3-(2,3-Dihydrobenzofuran-5-yl)- 1,2,3,4-tetrahydropyrrolo[3,4-b]quinolin-9-one

by Li, Xun, Branum, Shawn, Russell, Ronald K, Jiang, Weiqin, Sui, Zhihua
Published in Organic process research & development (01.09.2005)

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