Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alexander C. Wotal"'
Autor:
Alexander C. Wotal, Rachel J. Dunscomb, Benjamin R. Reiner, Robin P. Harkins, Ian A. Tonks, Adam J. Pearce
Publikováno v:
J Am Chem Soc
Pyrazoles are an important class of heterocycles found in a wide range of bioactive compounds and pharmaceuticals. Pyrazole synthesis often requires hydrazine or related reagents where an intact N-N bond is conservatively installed into a pyrazole pr
Autor:
Eric C. Hansen, Dylan J. Pedro, Stephane Caron, Jade D. Nelson, Nicholas J. Gower, Alexander C. Wotal, Daniel J. Weix
Publikováno v:
Nature chemistry
Ligands are essential for controlling the reactivity and selectivity of transition metal-catalyzed reactions. Access to large phosphine ligand libraries has become an essential tool for the application of metal-catalyzed reactions industrially, but t
Publikováno v:
Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals. 93
Autor:
Alexander C. Wotal, Daniel J. Weix
Publikováno v:
Organic Letters. 14:1476-1479
Unsymmetrical dialkyl ketones can be directly prepared by the nickel-catalyzed reductive coupling of carboxylic acid chlorides or (2-pyridyl)thioesters with alkyl iodides or benzylic chlorides. A wide variety of functional groups are tolerated by thi
Publikováno v:
Organometallics
Acylnickel(II) complexes feature prominently in cross-electrophile coupling (XEC) reactions that form ketones, yet their reactivity has not been systematically investigated. We present here our studies on the reactivity of acylnickel(II) complexes wi
Autor:
Alexander C. Wotal, Daniel J. Weix
Publikováno v:
ChemInform. 43
The procedure can be applied to a broad spectrum of substrates and includes even formation of hindered ketones.