Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Troy E. Zehnder"'
Autor:
Troy E. Zehnder, Daniel J. Nasrallah, Jarrod L. Stanley, John J. Kiernicki, Nathaniel K. Szymczak, Corinna S. Schindler
Publikováno v:
Organometallics. 42:479-485
Autor:
Neil Patrick Grimster, Lakshmaiah Gingipalli, Amber Balazs, Bernard Barlaam, Scott Boiko, Scott Boyd, Hannah Dry, Frederick W. Goldberg, Tim Ikeda, Tony Johnson, Sameer Kawatkar, Paul Kemmitt, Scott Lamont, Olivier Lorthioir, Adelphe Mfuh, Joe Patel, Andy Pike, Jon Read, Romulo Romero, Ujjal Sarkar, Li Sha, Iain Simpson, Kun Song, Qibin Su, Haixia Wang, David Watson, Allan Wu, Troy E. Zehnder, XiaoLan Zheng, Shaolu Li, Zhiqiang Dong, Dejian Yang, Yanwei Song, Peng Wang, Xuemei Liu, James E. Dowling, Scott D. Edmondson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db10a4172a7f6e477f5fdb84a232a7f
https://doi.org/10.2139/ssrn.4308038
https://doi.org/10.2139/ssrn.4308038
Autor:
Daniel J. Nasrallah, Troy E. Zehnder, Jacob R. Ludwig, Daniel C. Steigerwald, John J. Kiernicki, Nathaniel K. Szymczak, Corinna S. Schindler
Publikováno v:
Angew Chem Int Ed Engl
We describe the development of an efficient method for the olefination of hydrazones and oximes. The key design approach that enables this transformation is tuning of the energy/polarity of C=N π-bonds by employing electron withdrawing groups (NR(2)
Autor:
Troy E. Zehnder, Katie A. Rykaczewski, Mario A. Gaviria, Hannah L. Vonesh, Alistair D. Richardson, Emilia J. Groso, Corinna S. Schindler
Publikováno v:
Organic Letters. 22:2844-2848
Herein we describe the application of Lewis-acid-catalyzed carbonyl–olefin metathesis toward the synthesis of substituted tetrahydropyridines from commercially available amino acids as chiral pool ...
Publikováno v:
Advanced Synthesis & Catalysis. 362:365-369
Autor:
Katie A, Rykaczewski, Emilia J, Groso, Hannah L, Vonesh, Mario A, Gaviria, Alistair D, Richardson, Troy E, Zehnder, Corinna S, Schindler
Publikováno v:
Organic letters. 22(7)
Herein we describe the application of Lewis-acid-catalyzed carbonyl-olefin metathesis toward the synthesis of substituted tetrahydropyridines from commercially available amino acids as chiral pool reagents. This strategy relies on FeCl
Autor:
Hannah L. Vonesh, Corinna S. Schindler, Alistair D. Richardson, Mario A. Gaviria, Troy E. Zehnder, EmiliaJ. Groso, Katie A. Rykaczewski
Herein, we describe the application of Lewis acid-catalyzed carbonyl-olefin metathesis towards the synthesis of chiral, substituted tetrahydropyridines from commercially available amino acids as chiral pool reagents. This strategy relies on FeCl3 as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255e8456793e9ad451e77219b347c61b
https://doi.org/10.26434/chemrxiv.10007291.v1
https://doi.org/10.26434/chemrxiv.10007291.v1
Autor:
Corinna Schindler, Troy E. Zehnder, Alistair D. Richardson, Mario Gaviria, Hannah L. Vonesh, Emilia J. Groso, Katie Rykaczewski
Herein, we describe the application of Lewis acid-catalyzed carbonyl-olefin metathesis towards the synthesis of chiral, substituted tetrahydropyridines from commercially available amino acids as chiral pool reagents. This strategy relies on FeCl3 as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29dbd625c1b7b991ca51c30b6e558e21
https://doi.org/10.26434/chemrxiv.10007291
https://doi.org/10.26434/chemrxiv.10007291
Publikováno v:
Angewandte Chemie. 130:8818-8822
Autor:
Neil P. Grimster, Lakshmaiah Gingipalli, Bernard Barlaam, Qibin Su, XiaoLan Zheng, David Watson, Haixia Wang, Iain Simpson, Andy Pike, Amber Balazs, Scott Boiko, Timothy P. Ikeda, Anna C. Impastato, Natalie H. Jones, Sameer Kawatkar, Paul Kemmitt, Scott Lamont, Joe Patel, Jon Read, Ujjal Sarkar, Li Sha, Ronald C. Tomlinson, Haiyun Wang, David M. Wilson, Troy E. Zehnder, Lianghe Wang, Peng Wang, Frederick W. Goldberg, Wenlin Shao, Stephen Fawell, Hannah Dry, James E. Dowling, Scott D. Edmondson
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 30:127433
Spleen tyrosine kinase (SYK) is a non-receptor cytosolic kinase. Due to its pivotal role in B cell receptor and Fc-receptor signaling, inhibition of SYK has been targeted in a variety of disease areas. Herein, we report the optimization of a series o