Search Results - "Pennino, Scott" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis

Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis

by Patel, Nitinchandra D, Sieber, Joshua D, Tcyrulnikov, Sergei, Simmons, Bryan J, Rivalti, Daniel, Duvvuri, Krishnaja, Zhang, Yongda, Gao, Donghong A, Fandrick, Keith R, Haddad, Nizar, Lao, Kendricks So, Mangunuru, Hari P. R, Biswas, Soumik, Qu, Bo, Grinberg, Nelu, Pennino, Scott, Lee, Heewon, Song, Jinhua J, Gupton, B. Frank, Garg, Neil K, Kozlowski, Marisa C, Senanayake, Chris H
Published in ACS catalysis (02.11.2018)

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Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)‑3,3′-Cl2‑BINOL

Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)‑3,3′-Cl2‑BINOL

by Li, Ning, Li, Guisheng, Konrad, Michael, Kressierer, Christoph, Betzemeier, Bodo, Kosnik, Stephanie C., Wu, Lifen, Pennino, Scott, Lee, Heewon, Zhang, Yongda
Published in Organic process research & development (21.10.2022)

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Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by ( S )-3,3′-Cl 2 -BINOL

Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by ( S )-3,3′-Cl 2 -BINOL

by Li, Ning, Li, Guisheng, Konrad, Michael, Kressierer, Christoph, Betzemeier, Bodo, Kosnik, Stephanie C., Wu, Lifen, Pennino, Scott, Lee, Heewon, Zhang, Yongda
Published in Organic process research & development (21.10.2022)

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Practical Synthesis of Terminal Vinyl Fluorides

Practical Synthesis of Terminal Vinyl Fluorides

by Volchkov, Ivan, Powell, Brent V., Zatolochnaya, Olga V., Leung, Joyce C., Pennino, Scott, Wu, Lifen, Gonnella, Nina C., Bhaskararao, Bangaru, Kozlowski, Marisa C., Reeves, Jonathan T.
Published in Journal of organic chemistry (04.08.2023)

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Large Scale Practical Synthesis of Enantiomerically Pure cis-4-Amino-3-fluoro-1-methylpiperidine via Rhodium-Catalyzed Asymmetric Hydrogenation of a Tetrasubstituted Fluoroalkene

Large Scale Practical Synthesis of Enantiomerically Pure cis-4-Amino-3-fluoro-1-methylpiperidine via Rhodium-Catalyzed Asymmetric Hydrogenation of a Tetrasubstituted Fluoroalkene

by Qu, Bo, Saha, Anjan, Li, Guisheng, Zeng, Xingzhong, Wang, Xiaojun, Haddad, Nizar, Hou, Xiaowen, Lorenz, Jon C, Wu, Lifen, Pennino, Scott, Lee, Heewon, Song, Jinhua J, Senanayake, Chris H
Published in Organic process research & development (19.03.2021)

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Enantioselective Synthesis of α‑(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights

Enantioselective Synthesis of α‑(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights

by Qu, Bo, Mangunuru, Hari P. R, Tcyrulnikov, Sergei, Rivalti, Daniel, Zatolochnaya, Olga V, Kurouski, Dmitry, Radomkit, Suttipol, Biswas, Soumik, Karyakarte, Shuklendu, Fandrick, Keith R, Sieber, Joshua D, Rodriguez, Sonia, Desrosiers, Jean-Nicolas, Haddad, Nizar, McKellop, Keith, Pennino, Scott, Lee, Heewon, Yee, Nathan K, Song, Jinhua J, Kozlowski, Marisa C, Senanayake, Chris H
Published in Organic letters (02.03.2018)

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Building a Quaternary Stereogenic Center on Dihydroazaindole Carboxylic Acid through Scalable Process Development

Building a Quaternary Stereogenic Center on Dihydroazaindole Carboxylic Acid through Scalable Process Development

by Lee, Jaehee, Li, Guisheng, Zeng, Xingzhong, Haddad, Nizar, Abeyta, Vincent, Pennino, Scott, Wu, Lifen, Gao, Joe, Jiang, Qi, Lorenz, Jon C., Wang, Jun, Wu, Jiang-Ping, Brazzillo, Jason, Sarvestani, Max, Wang, Xiao-Jun, El-Awa, Ahmad, Leung, Joyce C., Qu, Bo, Tan, Zhulin, Song, Jinhua J.
Published in Organic process research & development (17.11.2023)

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Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4‑Quinolinyl Ethers and MoreApplication to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4‑Quinolinyl Ethers and MoreApplication to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

by Patel, Nitinchandra D, Wei, Xudong, Byrne, Denis, Narayanan, Bikshandarkoil A, Pennino, Scott, Sarvestani, Max, Saha, Anjan, Haddad, Nizar, Kapadia, Suresh, Lorenz, Jon C, DeCroos, Philomen, Ye, Andrew, Lee, Heewon, Grinberg, Nelu, Hossain, Azad, Busacca, Carl A, Yee, Nathan K, Senanayake, Chris H
Published in Journal of organic chemistry (02.07.2020)

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Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling

Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling

by Qu, Bo, Lee, Jaehee, Wu, Lifen, Saha, Anjan K., Li, Guisheng, Xu, Yibo, Tan, Zhulin, Brazzillo, Jason, Haddad, Nizar, Pennino, Scott, Rodriguez, Sonia, Lorenz, Jon C., Frutos, Rogelio, Sidhu, Kanwar P. S., Wang, Xiao-Jun, Zhang, Yongda, Senanayake, Chris H., Song, Jinhua J.
Published in Organic process research & development (16.09.2022)

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Synthesis of BI 894416 and BI 1342561, two potent and selective spleen tyrosine kinase inhibitors, labeled with carbon 14 and with deuterium

Synthesis of BI 894416 and BI 1342561, two potent and selective spleen tyrosine kinase inhibitors, labeled with carbon 14 and with deuterium

by Latli, Bachir, Hrapchak, Matt J., Samankumara, Lalith P., Fandrick, Daniel R., Pennino, Scott, Lee, Heewon, Song, Jinhua J.
Published in Journal of labelled compounds & radiopharmaceuticals (01.04.2023)

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A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

by Qu, Bo, Samankumara, Lalith P., Ma, Shengli, Fandrick, Keith R., Desrosiers, Jean-Nicolas, Rodriguez, Sonia, Li, Zhibin, Haddad, Nizar, Han, Zhengxu S., McKellop, Keith, Pennino, Scott, Grinberg, Nelu, Gonnella, Nina C., Song, Jinhua J., Senanayake, Chris H.
Published in Angewandte Chemie (International ed.) (22.12.2014)

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Structure Elucidation of a Complex Faldaprevir-(±)-α-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

Structure Elucidation of a Complex Faldaprevir-(±)-α-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

by Gonnella, Nina C., Rodriguez, Shirley A., Pennino, Scott, Norwood, Daniel
Published in Journal of heterocyclic chemistry (01.11.2016)

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Structure Elucidation of a Complex Faldaprevir-(±)-[alpha]-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

Structure Elucidation of a Complex Faldaprevir-(±)-[alpha]-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

by Gonnella, Nina C, Rodriguez, Shirley A, Pennino, Scott, Norwood, Daniel
Published in Journal of heterocyclic chemistry (01.11.2016)

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Process Development of the BACE Inhibitors BI 1147560 BS and BI 1181181 MZ

Process Development of the BACE Inhibitors BI 1147560 BS and BI 1181181 MZ

by Li, Guisheng, Tan, Zhulin, Xu, Yibo, Sidhu, Kanwar P. S., Qu, Bo, Herbage, Melissa A., Eriksson, Magnus C., Zeng, Xingzhong, Busacca, Carl A., Desrosiers, Jean-Nicolas, Hampel, Thomas, Niemeier, Oliver, Reichel, Carsten, Quynh Dang, Mai Thi, Schoerer, Marvin, Kemmer, Dirk, Eick, Melanie, Werle, Holger, Kim, Soojin, Li, Zhibin, Venkatraman, Shankar, Jia, Lanqi, Claremon, David A., Fuchs, Klaus, Heine, Niklas, Byrne, Denis, Narayanan, Bikshandarkoil, Sarvestani, Max, Johnson, Joe, Premasiri, Ajith, Nummy, Larry J., Lorenz, Jon C., Haddad, Nizar, Gonnella, Nina C., Pennino, Scott, Krawiec, Mariusz, Senanayake, Chris H., Buono, Frederic, Lee, Heewon, Hossain, Azad, Song, Jinhua J., Reeves, Jonathan T.
Published in Organic process research & development (16.12.2022)

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Synthesis of stable isotope‐labelled firocoxib

Synthesis of stable isotope‐labelled firocoxib

by Latli, Bachir, Gao, Amy, Kvaternick, Valerie, Tecle, Berhane, Pennino, Scott, Yee, Nathan K., Song, Jeff
Published in Journal of labelled compounds & radiopharmaceuticals (30.06.2020)

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Sulfone-Mediated S N Ar Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More-Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Sulfone-Mediated S N Ar Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More-Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

by Patel, Nitinchandra D, Wei, Xudong, Byrne, Denis, Narayanan, Bikshandarkoil A, Pennino, Scott, Sarvestani, Max, Saha, Anjan, Haddad, Nizar, Kapadia, Suresh, Lorenz, Jon C, DeCroos, Philomen, Ye, Andrew, Lee, Heewon, Grinberg, Nelu, Hossain, Azad, Busacca, Carl A, Yee, Nathan K, Senanayake, Chris H
Published in Journal of organic chemistry (02.07.2020)

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Development of a Scalable, Chromatography-Free Synthesis of t‑Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3‑Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

Development of a Scalable, Chromatography-Free Synthesis of t‑Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3‑Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

by Sieber, Joshua D, Rodriguez, Sonia, Frutos, Rogelio, Buono, Frederic, Zhang, Yongda, Li, Ning, Qu, Bo, Premasiri, Ajith, Li, Zhibin, Han, Zhengxu S, Xu, Yibo, Byrne, Denis, Haddad, Nizar, Lorenz, Jon, Grinberg, Nelu, Kurouski, Dmitry, Lee, Heewon, Narayanan, Bikshandarkoil, Nummy, Laurence, Mulder, Jason, Brown, Jack D, Granger, Alice, Gao, Joe, Krawiec, Mariusz, Williams, Zeena, Pennino, Scott, Song, Jinhua J, Hossain, Azad, Yee, Nathan K, Busacca, Carl, Roschangar, Frank, Xin, Yanchao, Mao, Zhantong, Zhang, Xinzhu, Hong, Yaping, Senanayake, Chris H
Published in Journal of organic chemistry (02.02.2018)

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Development of a Scalable, Chromatography-Free Synthesis of t -Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF 3 -Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

Development of a Scalable, Chromatography-Free Synthesis of t -Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF 3 -Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

by Sieber, Joshua D., Rodriguez, Sonia, Frutos, Rogelio, Buono, Frederic, Zhang, Yongda, Li, Ning, Qu, Bo, Premasiri, Ajith, Li, Zhibin, Han, Zhengxu S., Xu, Yibo, Byrne, Denis, Haddad, Nizar, Lorenz, Jon, Grinberg, Nelu, Kurouski, Dmitry, Lee, Heewon, Narayanan, Bikshandarkoil, Nummy, Laurence, Mulder, Jason, Brown, Jack D., Granger, Alice, Gao, Joe, Krawiec, Mariusz, Williams, Zeena, Pennino, Scott, Song, Jinhua J., Hossain, Azad, Yee, Nathan K., Busacca, Carl, Roschangar, Frank, Xin, Yanchao, Mao, Zhantong, Zhang, Xinzhu, Hong, Yaping, Senanayake, Chris H.
Published in Journal of organic chemistry (02.02.2018)

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Correction to “Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis”

Correction to “Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis”

by Patel, Nitinchandra D, Sieber, Joshua D, Tcyrulnikov, Sergei, Simmons, Bryan J, Rivalti, Daniel, Duvvuri, Krishnaja, Zhang, Yongda, Gao, Donghong A, Fandrick, Keith R, Haddad, Nizar, Lao, Kendricks So, Mangunuru, Hari P. R, Biswas, Soumik, Qu, Bo, Grinberg, Nelu, Pennino, Scott, Lee, Heewon, Song, Jinhua J, Gupton, B. Frank, Garg, Neil K, Kozlowski, Marisa C, Senanayake, Chris H
Published in ACS catalysis (01.02.2019)

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Identification of a process impurity formed during synthesis of a nevirapine analogue HIV NNRT inhibitor using LC/MS and forced degradation studies

Identification of a process impurity formed during synthesis of a nevirapine analogue HIV NNRT inhibitor using LC/MS and forced degradation studies

by Qiu, Fenghe, Pennino, Scott, Busacca, Carl A., Norwood, Daniel L.
Published in Journal of pharmaceutical and biomedical analysis (05.04.2009)

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