Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kristin Williams Fiori"'
Publikováno v:
Nature chemistry
While Nature excels at performing selective modifications of complex polyfunctional molecules through the use of tailoring enzymes, synthetic chemistry has lagged behind in this regard. In prior work, we have applied a biomimetic approach to this pro
Publikováno v:
Tetrahedron. 65:3042-3051
A detailed mechanistic investigation of the intramolecular dirhodium tetracarboxylate-catalyzed sulfamate ester C–H amination reaction is presented. These studies provide support for the formation of a sulfamate-derived iminoiodinane, which reacts
Autor:
J. Du Bois, Kristin Williams Fiori
Publikováno v:
Journal of the American Chemical Society. 129:562-568
Reaction methodology for intermolecular C-H amination of benzylic and 3 degrees C-H bonds is described. This process uses the starting alkane as the limiting reagent, gives optically pure tetrasubstituted amines through stereospecific insertion into
Publikováno v:
Angewandte Chemie. 116:4449-4452
Publikováno v:
Journal of the American Chemical Society. 126(47)
Analysis of the mechanism for Rh-mediated C−H amination has led to the development of a remarkably effective dinuclear Rh catalyst derived from 1,3-benzenedipropionic acid. This unique complex, Rh2(esp)2, is capable of promoting both intra- and int
Publikováno v:
ChemInform. 34
Access to stereochemically complex, polyfunctionalized amine derivatives is made possible using novel oxathiazinane N,O-acetal starting materials. These heterocycles are prepared through intramolecular sulfamate ester C-H insertion with a Rh(2+)-carb
Publikováno v:
Angewandte Chemie International Edition; Aug2004, Vol. 43 Issue 33, p4349-4352, 4p