Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Erica L. Ingalls"'
Publikováno v:
Journal of Organometallic Chemistry. 832:9-11
A new class of chiral Pd(II) complexes bearing a rigid, bidentate C,N-ligand are synthesized and characterized. The ligands are obtained in good yield via a simple five-step synthetic route beginning with cheap and commercially available amino alcoho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::514ca8d73272f98ce3cd8f81ca0a81c2
https://doi.org/10.1016/j.jorganchem.2017.01.008
https://doi.org/10.1016/j.jorganchem.2017.01.008
Publikováno v:
Angewandte Chemie International Edition. 54:4557-4560
The formation of highly substituted carbon centers using catalysis has been a widely sought after goal, but complexes of highly substituted carbon atoms with transition metals are rare, and the factors that affect the relative stability of complexes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f4f580a391a98f55cd8e0f470b026e
https://doi.org/10.1002/anie.201412033
https://doi.org/10.1002/anie.201412033
Publikováno v:
Angewandte Chemie International Edition. 52:13311-13313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::054b1b4f0c3f9f281d18da420af196f9
https://doi.org/10.1002/anie.201305766
https://doi.org/10.1002/anie.201305766
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b585893be4f341536b50031c36b5c119
https://doi.org/10.1002/chin.201421121
https://doi.org/10.1002/chin.201421121
Publikováno v:
Journal of the American Chemical Society. 135(24)
An enantioselective Pd-catalyzed vicinal diamination of unactivated alkenes using N-fluorobenzenesulfonimide as both an oxidant and a source of nitrogen is reported. The use of Ph-pybox and Ph-quinox ligands afforded differentially protected vicinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebeef25a4c735a62c3918694897bd3ac
https://pubmed.ncbi.nlm.nih.gov/23734771
https://pubmed.ncbi.nlm.nih.gov/23734771
Autor:
Sinisa Bjelic, Forrest E. Michael, David Baker, Scott Lew, Gert Kiss, Jasmine L. Gallaher, Helena M. Lovick, John F. Hunt, Gaetano T. Montelione, Erica L. Ingalls, Lucas G. Nivón, Kendall N. Houk, Nihan Çelebi-Ölçüm, Jayaraman Seetharaman, Carolyn F. Rosewall
The Morita-Baylis-Hillman reaction forms a carbon-carbon bond between the alpha carbon of a conjugated carbonyl compound and a carbon electrophile. The reaction mechanism involves Michael addition of a nucleophile catalyst at the carbonyl beta carbon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec4d63de181fde4358467b377a9b20f
https://europepmc.org/articles/PMC3647451/
https://europepmc.org/articles/PMC3647451/
