Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Tiffany, Piou"'
Autor:
Caitlin R. Lacker, Travis J. DeLano, Emily P. Chen, Jongrock Kong, Kevin M. Belyk, Tiffany Piou, Sarah E. Reisman
Publikováno v:
Journal of the American Chemical Society. 144:20190-20195
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::271f62a198aac6b93fb2c429e32705bb
https://doi.org/10.1021/jacs.2c07917
https://doi.org/10.1021/jacs.2c07917
Autor:
Caitlin R, Lacker, Travis J, DeLano, Emily P, Chen, Jongrock, Kong, Kevin M, Belyk, Tiffany, Piou, Sarah E, Reisman
Publikováno v:
Journal of the American Chemical Society. 144(44)
An asymmetric cross-coupling of α
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab0c725d4ca41124c28e07320821098c
https://pubmed.ncbi.nlm.nih.gov/36288571
https://pubmed.ncbi.nlm.nih.gov/36288571
Autor:
Tiffany Piou, Louis-Charles Campeau
Publikováno v:
Nature Chemistry. 13:1027-1028
Aziridines — three-membered nitrogen-containing heterocycles — are important synthetic targets, but N-alkyl aziridines are difficult to synthesize. Now, an electrochemical method, involving a dicationic intermediate, enables the coupling of alken
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f50f84ae006cbbc2d09300e36f92cbd7
https://doi.org/10.1038/s41557-021-00819-7
https://doi.org/10.1038/s41557-021-00819-7
Publikováno v:
Organic letters. 23(6)
A practical approach toward the synthesis of 2-arylazoles via direct arylation is described. The transformation relies on a Pd/Cu cocatalyst system that operates with low catalyst loadings. The reaction conditions were found to be tolerant of a wide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77dfcece5b2fff9da77c6f49693760bd
https://pubmed.ncbi.nlm.nih.gov/33667104
https://pubmed.ncbi.nlm.nih.gov/33667104
Autor:
Robert S. Paton, Kelvin E. Jackson, Christopher D. Rithner, Tomislav Rovis, Natthawat Semakul, Brian S. Newell, Trevor D. Taggart, Tiffany Piou, Maria Romanova-Michaelides, Fedor Romanov-Michailidis
Publikováno v:
Journal of the American Chemical Society. 139:1296-1310
Cp(X)Rh(III)-catalyzed C-H functionalization reactions are a proven method for the efficient assembly of small molecules. However, rationalization of the effects of cyclopentadienyl (Cp(X)) ligand structure on reaction rate and selectivity has been v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb0cb46863c772e94aa411b1edee1586
https://doi.org/10.1021/jacs.6b11670
https://doi.org/10.1021/jacs.6b11670
Autor:
Tiffany Piou, Fedor Romanov-Michailidis, Maria Romanova-Michaelides, Kelvin E. Jackson, Natthawat Semakul, Trevor D. Taggart, Brian S. Newell, Christopher D. Rithner, Robert S. Paton, Tomislav Rovis
Publikováno v:
Journal of the American Chemical Society. 142:7709-7709
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10c0669e37d2aaa31c4d9525bfa2ca9e
https://doi.org/10.1021/jacs.0c00951
https://doi.org/10.1021/jacs.0c00951
Autor:
Tomislav Rovis, Melissa A. Ashley, Maria Romanova-Michaelides, Fedor Romanov-Michailidis, Tiffany Piou
Publikováno v:
Journal of the American Chemical Society. 140(30)
The design of stereodivergent transformations is of great interest to the synthetic community as it allows to funnel a given reaction pathway toward one stereochemical outcome or another by only minor adjustments of the reaction setup. Herein, we pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::624e26121db397cd4094fa1f8c21bfb1
https://pubmed.ncbi.nlm.nih.gov/30033723
https://pubmed.ncbi.nlm.nih.gov/30033723
Autor:
Tomislav Rovis, Tiffany Piou
Publikováno v:
Nature
Alkenes are the most ubiquitous prochiral functional groups--those that can be converted from achiral to chiral in a single step--that are accessible to synthetic chemists. For this reason, difunctionalization reactions of alkenes (whereby two functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::148c016868b4ee709bbf378e56f87711
https://doi.org/10.1038/nature15691
https://doi.org/10.1038/nature15691
Autor:
Tiffany Piou
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::610fde532a5af24bb6ffa6db6f76d268
https://doi.org/10.1002/047084289x.rn01943
https://doi.org/10.1002/047084289x.rn01943
Publikováno v:
Organic Letters. 17:334-337
A Pd(0)-catalyzed double cyclization of easily available o-bromoanilides leading to strained [3,4]-fused oxindoles was developed. The reaction proceeded through a highly ordered sequence involving key carbopalladation, 1,4-Pd migration, and C(sp(2))-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a43457a0130d9e5122acee3759ffaccf
https://doi.org/10.1021/ol503442n
https://doi.org/10.1021/ol503442n