Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Robert J, Phipps"'
Publikováno v:
Journal of the American Chemical Society. 145:7516-7527
Alkene aziridination is a highly versatile transformation for the construction of chiral nitrogen-containing compounds. Inspired by the success of analogous substrate-directed epoxidations, we report an enantioselective aziridination of alkenyl alcoh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c620209fddd2c839b1c82ca75c90e4
https://doi.org/10.1021/jacs.3c00693
https://doi.org/10.1021/jacs.3c00693
Autor:
Robert J. Phipps
Publikováno v:
Supramolecular Catalysis. :117-132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48318fd1b1e16c106855909d4ab3865e
https://doi.org/10.1002/9783527832033.ch9
https://doi.org/10.1002/9783527832033.ch9
Publikováno v:
Journal of the American Chemical Society
The formation of arene C-N bonds directly from C-H bonds is of great importance and there has been rapid recent development of methods for achieving this through radical mechanisms, often involving reactive N-centered radicals. A major challenge asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6724c5b25b2c84bb5295badd71404128
https://doi.org/10.1021/jacs.1c05531
https://doi.org/10.1021/jacs.1c05531
Autor:
Robert Pearce-Higgins, Larissa N. Hogenhout, Philip J. Docherty, David M. Whalley, Padon Chuentragool, Najung Lee, Nelson Y. S. Lam, Thomas M. McGuire, Damien Valette, Robert J. Phipps
Publikováno v:
Journal of the American Chemical Society. 144(33)
Axial chirality features prominently in molecules of biological interest as well as chiral catalyst designs, and atropisomeric 2,2'-biphenols are particularly prevalent. Atroposelective metal-catalyzed cross-coupling is an attractive and modular appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab822f62364bcb0fae6f38f2a517be1
https://pubmed.ncbi.nlm.nih.gov/35969692
https://pubmed.ncbi.nlm.nih.gov/35969692
Publikováno v:
Angewandte Chemie. 134
Ortho-sulfonyl anilines are important building blocks for a range of applications. We report the discovery of an aromatic rearrangement reaction of O-(arenesulfonyl)hydroxylamines which leads directly to ortho-sulfonyl anilines through formation of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21cc1f1edefa0c05f650bffd470f7ceb
https://doi.org/10.1002/ange.202204025
https://doi.org/10.1002/ange.202204025
Publikováno v:
Journal of the American Chemical Society
Minisci-type reactions constitute one of the most powerful methods for building up complexity around basic heteroarenes. The most desirable variants involve formal oxidative coupling of a C-H bond on each partner, leading back to the simplest possibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c43a24d8644c50a95beb9cf0b00e1d
https://doi.org/10.1021/jacs.1c01556
https://doi.org/10.1021/jacs.1c01556
Publikováno v:
Remote C-H Bond Functionalizations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3585c6f17fc28e1edb43bc6a8adf0098
https://doi.org/10.1002/9783527824137.ch6
https://doi.org/10.1002/9783527824137.ch6
Publikováno v:
Journal of the American Chemical Society
Use of attractive noncovalent interactions between ligand and substrate is an emerging strategy for controlling positional selectivity. A key question relates to whether fine control on molecules with multiple, closely spaced reactive positions is ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e1aa91c2addefdafc728773c1e72fc
https://doi.org/10.1021/jacs.0c11056
https://doi.org/10.1021/jacs.0c11056
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed4231bf3b073ed9056ae0b428d784d5
https://doi.org/10.1002/047084289x.rn02345
https://doi.org/10.1002/047084289x.rn02345
Autor:
Barbara W. Hadrys, Robert J. Phipps
Publikováno v:
Synlett. 32:179-184
Minisci-type reactions comprise an important class of reactions for the direct functionalization of basic heterocyclic compounds. On certain heterocycles, such as quinolines, Minisci-type reactions face a regioselectivity choice which often results i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01460feaa9f25f6f0e94becd003e61b1
https://doi.org/10.1055/s-0040-1707888
https://doi.org/10.1055/s-0040-1707888