Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ka Hou Hoi"'
Publikováno v:
Angewandte Chemie International Edition. 51:3314-3332
Palladium-catalyzed cross-coupling reactions enable organic chemists to form C-C bonds in targeted positions and under mild conditions. Although phosphine ligands have been intensively researched, in the search for even better cross-coupling catalyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd1ce9da1a52f55b942cafc98c67179e
https://doi.org/10.1002/anie.201106131
https://doi.org/10.1002/anie.201106131
Die Entwicklung raumerfüllender Palladium-NHC-Komplexe für anspruchsvollste Kreuzkupplungsreaktionen
Publikováno v:
Angewandte Chemie. 124:3370-3388
Palladiumkatalysierte Kreuzkupplungen versetzten Organiker in die Lage, C-C-Bindungen gezielt und unter milden Reaktionsbedingungen zu einzufuhren. Wahrend Phosphanliganden in diesen Umsetzungen am intensivsten erforscht wurden, sind seit kurzem auf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e087387924510ec93f77ab20b6863e1
https://doi.org/10.1002/ange.201106131
https://doi.org/10.1002/ange.201106131
Autor:
Michael G. Organ, Ka Hou Hoi
Publikováno v:
Chemistry - A European Journal. 18:804-807
This base is just right! A new base, potassium 2,2,5,7,8-pentamethylchroman-6-oxide, for Pd-catalysed amination has been rationally designed that has sufficient basicity to efficiently deprotonate the intermediate aryl palladium ammonium complex, lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5575d6a7d1afc4dfc88c5b23602f3fff
https://doi.org/10.1002/chem.201103284
https://doi.org/10.1002/chem.201103284
Publikováno v:
Chemistry - A European Journal. 18:145-151
The amination of aryl chlorides with various aniline derivatives using the N-heterocyclic carbene-based Pd complexes Pd-PEPPSI-IPr and Pd-PEPPSI-IPent (PEPPSI=pyridine, enhanced precatalyst, preparation, stabilization, and initiation; IPr=diisopropyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::882ac65ecd44711abc898d6cc9a34684
https://doi.org/10.1002/chem.201102428
https://doi.org/10.1002/chem.201102428
Publikováno v:
Chemistry – A European Journal. 17:3086-3090
Pd-PEPPSI-IPent, a recently-developed N-heterocyclic carbene (NHC) complex, has been evaluated in amination reactions with secondary amines and it has shown superb reactivity under the most mildly basic reaction conditions. Rate and computational stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75a85db07f9a451cd71d2aca76b72ad0
https://doi.org/10.1002/chem.201002988
https://doi.org/10.1002/chem.201002988
Publikováno v:
Chemistry - A European Journal. 19:843-845
Third times a charm: A new Pd-NHC catalyst, Pd-PEPPSI-IPent(Cl), has been developed for applications in amination reactions for the preparation of triarylamines. The catalyst can be used under mild conditions (carbonate base/dioxane, 80 °C) to perfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bca2a94c50431dd627a6b205a43100d0
https://doi.org/10.1002/chem.201203379
https://doi.org/10.1002/chem.201203379
Publikováno v:
ChemInform. 44
Third times a charm: A new Pd-NHC catalyst, Pd-PEPPSI-IPent(Cl), has been developed for applications in amination reactions for the preparation of triarylamines. The catalyst can be used under mild conditions (carbonate base/dioxane, 80 °C) to perfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c819c91e8e917c5bbbf03b6ea73d55
https://doi.org/10.1002/chin.201321066
https://doi.org/10.1002/chin.201321066
Publikováno v:
ChemInform. 43
Palladium-catalyzed cross-coupling reactions enable organic chemists to form C-C bonds in targeted positions and under mild conditions. Although phosphine ligands have been intensively researched, in the search for even better cross-coupling catalyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c243e937a80fcca45759a3e2705c1fe
https://doi.org/10.1002/chin.201232239
https://doi.org/10.1002/chin.201232239
Publikováno v:
ChemInform. 40
Incredible Bulk: A series of N-heterocyclic carbene catalysts (see picture) were prepared and evaluated in the Suzuki-Miyaura reaction. A variety of sterically encumbered tetra-ortho-substituted biaryl products were formed from unreactive aryl chlori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9ca905b92dbea58f3a3599f712ee5ab
https://doi.org/10.1002/chin.200928072
https://doi.org/10.1002/chin.200928072
Publikováno v:
Angewandte Chemie (International ed. in English). 48(13)
Incredible Bulk: A series of N-heterocyclic carbene catalysts (see picture) were prepared and evaluated in the Suzuki-Miyaura reaction. A variety of sterically encumbered tetra-ortho-substituted biaryl products were formed from unreactive aryl chlori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b7db247d3b8b6c95af6f3969210339
https://pubmed.ncbi.nlm.nih.gov/19226587
https://pubmed.ncbi.nlm.nih.gov/19226587