Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Thomas R. Wagler"'
Autor:
Thomas R. Wagler, Surendra P. Singh, Philomen de Croos, Roger P. Bakale, Charles P. Vandenbossche
Publikováno v:
Organic Process Research & Development. 14:921-925
The synthesis of the drug candidate (S)-oxybutynin hydrochloride 1 is described. The procedure involves initial activation of (S)-cyclohexylmandelic acid 2, using isobutylchloroformate, followed by...
Autor:
Thomas H. Williams, Wayne S. Hammond, Thomas R. Wagler, David L. Coffen, Gino J. Sasso, Voldemar Toome, Larry E. Nitzsche, Eugene Ho, Carlo Nocka
Publikováno v:
Journal f�r Praktische Chemie/Chemiker-Zeitung. 335:135-142
Thirteen Schiff base salts in the class of compounds represented by retinal pyrrolidinium perchlorate were prepared (most of them for the first time), fully characterized analytically and spectroscopically, and examined in the 30–100 GHz range with
Publikováno v:
Journal of the American Chemical Society. 112:4568-4570
Transition-metal-catalyzed transfer of oxygen atoms to organic substrates is of interest in the study of bioinorganic mechanisms and the development of efficient catalysts for laboratory and industrial organic synthesis. Certain nickel(II) catalysts
Autor:
Thomas R. Wagler, Cynthia J. Burrows
Publikováno v:
Tetrahedron Letters. 29:5091-5094
An optically active dioxo-cyclam macrocycle bearing two benzyl side chains derived from phenylalanine has been synthesized; its Ni(II) complex catalyzes the oxidation of olefins using hypochlorite under phase transfer conditions.
Autor:
Lucy Shen, Jeffrey S. Albert, Therese M. Roy, Heungsik Yoon, Cynthia J. Burrows, Thomas R. Wagler, Joanne F. Kinneary
Publikováno v:
Journal of Inclusion Phenomena and Molecular Recognition in Chemistry. 7:155-168
New nickel catalysts have been developed for the oxidation of alkenes to epoxides, alcohols, aldehydes and ketones. Mechanistic studies indicate that the oxidation reactions are very sensitive to the nature of the catalyst; only certain ligands inclu
Publikováno v:
The Journal of Organic Chemistry. 54:1584-1589
Publikováno v:
Tetrahedron Letters. 29:877-880
A series of optically active Ni(II)-cyclam complexes are active catalysts for the PhIO oxidation of alkenes; labeling and stereochemical studies suggest important mechanistic differences from heme catalysts.
Autor:
Joanne F. Kinneary, Therese M. Roy, Jeffrey S. Albert, Heungsik Yoon, Thomas R. Wagler, Lucy Shen, Cynthia J. Burrows
Publikováno v:
United States-Japan Seminar on Host-Guest Chemistry ISBN: 9789401069250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00917ad6edb7fb44cb194560ae39d2aa
https://doi.org/10.1007/978-94-009-0969-4_18
https://doi.org/10.1007/978-94-009-0969-4_18
Publikováno v:
ChemInform. 19
A series of optically active Ni(II)-cyclam complexes are active catalysts for the PhIO oxidation of alkenes; labeling and stereochemical studies suggest important mechanistic differences from heme catalysts.
Autor:
Cynthia J. Burrows, Thomas R. Wagler
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :277
An optically active cyclam ligand bearing a functionalized side chain appended to a ring carbon and its nickel(II) complex are readily prepared from a diamino acid precursor.