Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Daniel R. Fandrick"'
Autor:
Jinhua J. Song, Jonathan T. Reeves, Daniel R. Fandrick, Zhulin Tan, Nathan K. Yee, Chris H. Senanayake
Publikováno v:
ARKIVOC, Vol 2010, Iss 1, Pp 390-449 (2010)
Externí odkaz:
https://doaj.org/article/79030d9424644986af116dc3d2a086ba
Autor:
Bachir Latli, Matt J. Hrapchak, Lalith P. Samankumara, Daniel R. Fandrick, Scott Pennino, Heewon Lee, Jinhua J. Song
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 66:155-168
Autor:
Suttipol Radomkit, Daniel R. Fandrick, Stefan Braith, Chris H. Senanayake, Arindom Chatterjee, Keith R. Fandrick, Carl A. Busacca, Nitinchandra D. Patel
Publikováno v:
The Journal of Organic Chemistry. 86:4877-4882
A mild and nonreversible tert-butylation of alcohols and phenols can be achieved in high yields using the noncoordinating acid–base catalyst [bis(trifluoromethane)sulfonimide and 2,6-lutidine] with...
Autor:
Keith R, Fandrick, Nitinchandra D, Patel, Suttipol, Radomkit, Arindom, Chatterjee, Stefan, Braith, Daniel R, Fandrick, Carl A, Busacca, Chris H, Senanayake
Publikováno v:
The Journal of organic chemistry. 86(6)
A mild and nonreversible
Autor:
Omar Apolinar, Daniel R. Fandrick, Rei Matsuura, Jinhua Song, Mingyu Liu, Tianhua Tang, Olga V. Zatolochnaya, Carl A. Busacca, Keary M. Engle, Chris H. Senanayake, Bo Qu
Publikováno v:
J Am Chem Soc
Selective carbon–carbon (C–C) bond formation in chemical synthesis generally requires pre-functionalized building blocks. However, the requisite pre-functionalization steps undermine the efficiency of multi-step synthetic sequences, which is part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e37ce7058e5bab980d3b85f841be6ef9
https://doi.org/10.26434/chemrxiv.13083419.v1
https://doi.org/10.26434/chemrxiv.13083419.v1
Autor:
Nitinchandra D. Patel, Marisa C. Kozlowski, Osvaldo Gutierrez, Chris H. Senanayake, Carl A. Busacca, Keith R. Fandrick, C. Avery Sader, Daniel R. Fandrick, Yike Zou
Publikováno v:
Organic Letters
A copper-catalyzed site-selective propargylation/allenylation reaction toward carbonyl compounds has been mechanistically investigated using a computational approach. Different reaction pathways and catalytic cycles were investigated. Control of the
Autor:
Zhidong Chen, Carl A. Busacca, Shengli Ma, Xingzhong Zeng, Peter Allen Nemoto, Paige E. Mahaney, Jason A. Mulder, Chris H. Senanayake, Jun Wang, Nitinchandra D. Patel, Zhibin Li, Todd Bosanac, Daniel R. Fandrick, Jean-Nicolas Desrosiers, Heewon Lee, Sonia Rodriguez, Jon C. Lorenz, Nathan K. Yee, Joe Gao, Nelu Grinberg, Hidenori Takahashi, Alessandra Bartolozzi, Jinhua J. Song, Keith R. Fandrick
Publikováno v:
Organic Process Research & Development. 21:1427-1434
A practical and efficient synthesis of the FLAP inhibitor 1 was developed addressing multiple scale-up and safety concerns posed by the established synthesis and utilized a resolution strategy (replacing supercritical fluid chromatography (SFC) separ
Autor:
Chris H. Senanayake, Daniel R. Fandrick, Keith R. Fandrick, Christine A. Hart, James T. Masters, Max Sarvestani, Ifeanyi S. Okafor, Nelu Grinberg, Heewon Lee, Sanjit Sanyal, Jennifer L. Stockdill, Michael A. Mercadante, Nina C. Gonnella
Publikováno v:
Organic Letters. 18:6192-6195
The copper-catalyzed asymmetric propargylation of cyclic aldimines is reported. The influence of the imine trimer to inhibit the reaction was identified, and equilibrium constants between the monomer and trimer were determined for general classes of
Autor:
Veronica V. Angeles‐Dunham, Dimitry Kurouski, Nelu Grinberg, Joshua D. Sieber, Chris H. Senanayake, Nathan K. Yee, Daniel R. Fandrick, Anita E. Mattson, Heewon Lee, Nizar Haddad, Jinhua J. Song, Divya Chennamadhavuni
Publikováno v:
Advanced Synthesis & Catalysis. 358:3062-3068
Autor:
B. Frank Gupton, Daniel Rivalti, Keith R. Fandrick, James T. Masters, Nizar Haddad, Daniel R. Fandrick, Joshua D. Sieber, Heewon Lee, Chris H. Senanayake, Nathan K. Yee, Melissa A. Herbage
Publikováno v:
Organic Chemistry Frontiers. 3:1149-1153
A Rh-catalysed asymmetric conjugate addition of aryl boronic acids to β-substituted nitroalkenes was developed employing a P-chiral P-alkene hybrid bidentate ligand with enantioselectivities of up to 94:6 er. DFT modelling of the transition state fo