Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Krishna Nimmagadda"'
Autor:
Krishna Nimmagadda, Susan Pancrazi, Anthony Martino, Eric Coleman, Narasa Madam, Nicole Goekler, Claudia Rodriguez, Sarah Kramer, Bharat Magu, Deb Aders
Publikováno v:
The Joint Commission Journal on Quality and Patient Safety.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecdbb3deb40ef18373cd10e7d221adcd
https://doi.org/10.1016/j.jcjq.2023.04.006
https://doi.org/10.1016/j.jcjq.2023.04.006
Autor:
Debottam Dasgupta, Siva Sankar Bondigela, Arun Vinodini, Srinivas Kalidindi, Selin Aytar, Rajappa Vaidyanathan, Satish Korapati, Francisco González-Bobes, Prantik Maity, Aravind S. Gangu, Alla Venu, William P. Gallagher, Sri Krishna Nimmagadda, Noormohamed Abdul Malik
Publikováno v:
Organic Process Research & Development. 24:1141-1148
We describe the development and scale-up of a nickel-catalyzed reductive cross-electrophile coupling reaction between a substituted 2-chloropyridine and ethyl 3-chloropropanoate using manganese dus...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ca6ee2e61a65e8ccbb306ffbca2dbfc
https://doi.org/10.1021/acs.oprd.0c00134
https://doi.org/10.1021/acs.oprd.0c00134
Autor:
Jason S. Chen, De-Wei Gao, Omar Apolinar, Mingyu Liu, Peng Liu, Sri Krishna Nimmagadda, Malkanthi K. Karunananda, Keary M. Engle
Publikováno v:
Angewandte Chemie. 131:3963-3967
A palladium(II)-catalyzed enantioselective α-alkylation of azlactones with nonconjugated alkenes is described. The reaction employs a chiral BINOL-derived phosphoric acid as the source of stereoinduction, and a cleavable bidentate directing group ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5be8349986ce96b32dc5ffa85f580d12
https://doi.org/10.1002/ange.201814272
https://doi.org/10.1002/ange.201814272
Autor:
Jon C. Antilla, Sri Krishna Nimmagadda
Publikováno v:
Catalysis with Earth-abundant Elements ISBN: 9781788011181
This chapter summarizes a variety of the important advances using chiral phosphoric acids as catalysts for enantioselectively controlled reactions (asymmetric catalysis). It will be evident that the variety of substrates and nucleophiles is quite lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b053aa05565d18eba9cc5076bcc4984f
https://doi.org/10.1039/9781788012775-00334
https://doi.org/10.1039/9781788012775-00334
Publikováno v:
Org Biomol Chem
Through the combined action of palladium catalysts and chiral phosphoric acids (CPAs) a variety of catalytic asymmetric reactions have been realized during the past decade, including allylation, alkene functionalization, and C-H activation. This revi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71b348fd864b03af93532278df81cc85
https://europepmc.org/articles/PMC7032947/
https://europepmc.org/articles/PMC7032947/
Autor:
Lukasz Woztas, Steven E. Wheeler, Sri Krishna Nimmagadda, Sharath Chandra Mallojjala, Jon C. Antilla
Publikováno v:
Angewandte Chemie. 129:2494-2498
Axially chiral cyclohexylidene oxime ethers exhibit unique chirality because of the restricted rotation of C=N. The first catalytic enantioselective synthesis of novel axially chiral cyclohexylidene oximes has been developed by catalytic desymmetriza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e33512868603e5772ec77c07c3ca04a
https://doi.org/10.1002/ange.201611602
https://doi.org/10.1002/ange.201611602
Autor:
De-Wei Gao, Sri Krishna Nimmagadda, Yiyang Xiao, Benjamin F. Cravatt, Jose M. Medina, Radu M. Suciu, Ekaterina V. Vinogradova, Keary M. Engle
Nucleophilic attack on carbon-based electrophiles is a central reactivity paradigm in chemistry and biology. The steric and electronic properties of the electrophile dictate its reactivity with different nucleophiles of interest, allowing the opportu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c284bdccdb8ce64d57947296abba3e0
https://europepmc.org/articles/PMC6033665/
https://europepmc.org/articles/PMC6033665/
Publikováno v:
Organic Letters
A highly efficient method for the enantioselective one-pot synthesis of 1,3-oxazolidines and 1,3-oxazinanes has been reported. The reaction proceeds via the formation of hemiaminal intermediates obtained by the enantioselective addition of respective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a0a1b7cffebd33e1e9451156bcffc6
https://doi.org/10.1021/ol501789c
https://doi.org/10.1021/ol501789c
Publikováno v:
Asymmetric Dearomatization Reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::847e8b5e40e71aeef87a547ee6f072b6
https://doi.org/10.1002/9783527698479.ch8
https://doi.org/10.1002/9783527698479.ch8
Publikováno v:
The Journal of Supercomputing. 59:1360-1378
The cardiac bidomain model is a popular approach to study electrical behavior of tissues and simulate interactions between the cells by solving partial differential equations. The iterative and data parallel model is an ideal match for the parallel a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d4109c4a4552c8d9d8fe26979b80a4a
https://doi.org/10.1007/s11227-010-0540-x
https://doi.org/10.1007/s11227-010-0540-x