Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Katherine I. Burton"'
Publikováno v:
Angewandte Chemie International Edition. 60:16366-16371
Our ongoing search for underdeveloped functional group combinations has brought to light α-fluorinated aminoalkylboronic acids, a new class of molecules featuring the B-CF linkage. These compounds can now be generated from secondary amines and α-bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8942689fbbed8dbeef5e44bf1b49c4b5
https://doi.org/10.1002/anie.202104133
https://doi.org/10.1002/anie.202104133
Autor:
Saurabh S. Chitnis, Douglas W. Stephan, Katherine I. Burton, Andrew R. Jupp, Maotong Xu, Maegan S. E. Ong
Publikováno v:
Angewandte Chemie. 131:5763-5767
A series of thirty-three N,N'-diaryl, dialkyl, and alkyl-aryl ureas have been prepared in pyridine or toluene by reaction of silylamines with CO2 . This protocol is shown to provide facile access to 13 C-labeled ureas, as well as chiral and macrocycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::190b37feb04b4a0547bc31b1c56128a5
https://doi.org/10.1002/ange.201900058
https://doi.org/10.1002/ange.201900058
Autor:
Douglas W. Stephan, Frank Glorius, Tobias Wagener, Ryan Andrews, Katherine I. Burton, Alexander E. Waked, Iris Elser
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(45)
The development of novel Lewis acids derived from bipyridinium and phenanthrolinium dications is reported. Calculations of Hydride Ion Affinity (HIA) values indicate high carbon-based Lewis acidity at the ortho and para positions. This arises in part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eddf48b06adce0f0e3bcde9a52cb4586
https://pubmed.ncbi.nlm.nih.gov/34107119
https://pubmed.ncbi.nlm.nih.gov/34107119
Autor:
David A. Petrone, Katherine I. Burton, José F. Rodríguez, Ivan Franzoni, Mark Lautens, Ina Scheipers
Publikováno v:
Organic Letters. 20:6915-6919
The use of ammonium halide salts as metal hydride precursors in a new Pd-catalyzed cycloisomerization of 1,6-diynes, which affords unexplored silylated 2-azafluorenes, is reported. This cascade process includes the addition of a Pd-hydride species to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c436b24bdf1bc36d8a13bad8037639
https://doi.org/10.1021/acs.orglett.8b03057
https://doi.org/10.1021/acs.orglett.8b03057
Publikováno v:
Angewandte Chemie International Edition. 57:13927-13930
An enantioselective copper-catalyzed intramolecular borylacylation is reported. The reaction proceeds through an initial enantioselective borylcupration of the styrene, followed by a nucleophilic attack on the tethered carbamoyl chloride. The product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d0e66a36309cc4325133e6b5a89cf1
https://doi.org/10.1002/anie.201808460
https://doi.org/10.1002/anie.201808460
Autor:
Maotong, Xu, Andrew R, Jupp, Maegan S E, Ong, Katherine I, Burton, Saurabh S, Chitnis, Douglas W, Stephan
Publikováno v:
Angewandte Chemie (International ed. in English). 58(17)
A series of thirty-three N,N'-diaryl, dialkyl, and alkyl-aryl ureas have been prepared in pyridine or toluene by reaction of silylamines with CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7c4149a8a5cb9756312ad8f565565a2
https://pubmed.ncbi.nlm.nih.gov/30821888
https://pubmed.ncbi.nlm.nih.gov/30821888
Autor:
Soor, Harjeet S.1 (AUTHOR), Diaz, Diego B.1 (AUTHOR), Burton, Katherine I.1 (AUTHOR), Yudin, Andrei K.1 (AUTHOR) andrei.yudin@utoronto.ca
Publikováno v:
Angewandte Chemie. Jul2021, Vol. 133 Issue 30, p16502-16507. 6p.
Autor:
Xu, Maotong1, Jupp, Andrew R.1, Ong, Maegan S. E.1, Burton, Katherine I.1, Chitnis, Saurabh S.1, Stephan, Douglas W.1 dstephan@chem.utoronto.ca
Publikováno v:
Angewandte Chemie. 4/16/2019, Vol. 131 Issue 17, p5763-5767. 5p.
Autor:
Whyte, Andrew1, Burton, Katherine I.1, Zhang, Jingli1,2, Lautens, Mark1 mlautens@chem.utoronto.ca
Publikováno v:
Angewandte Chemie. 10/15/2018, Vol. 130 Issue 42, p14123-14126. 4p.