Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Raissa M. Trend"'
Autor:
Raissa M. Trend, Ryan M. McFadden, Eric M. Ferreira, Jeffrey T. Bagdanoff, Daniel D. Caspi, Brian M. Stoltz, David C. Ebner
Publikováno v:
Chemistry - A European Journal. 15:12978-12992
The first palladium-catalyzed enantioselective oxidation of secondary alcohols has been developed, utilizing the readily available diamine (-)-sparteine as a chiral ligand and molecular oxygen as the stoichiometric oxidant. Mechanistic insights regar
Autor:
Raissa M. Trend, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 130:15957-15966
The chiral ligand (-)-sparteine and PdCl(2) catalyze the enantioselective oxidation of secondary alcohols to ketones and thus effect a kinetic resolution. The structural features of sparteine that led to the selectivity observed in the reaction were
Autor:
David C. Ebner, Raissa M. Trend, Cédric Genet, Matthew J. McGrath, Peter O'Brien, Brian M. Stoltz
Publikováno v:
Angewandte Chemie. 120:6467-6470
Publikováno v:
Journal of the American Chemical Society. 127:17778-17788
Oxidative cyclizations of a variety of heteroatom nucleophiles onto unactivated olefins are catalyzed by palladium(II) and pyridine in the presence of molecular oxygen as the sole stoichiometric oxidant in a nonpolar solvent (toluene). Reactivity stu
Autor:
Ryan M. McFadden, Jeffrey T. Bagdanoff, Brian M. Stoltz, Eric M. Ferreira, David C. Ebner, Raissa M. Trend, Daniel D. Caspi
Publikováno v:
ChemInform. 41
The first palladium-catalyzed enantioselective oxidation of secondary alcohols has been developed, utilizing the readily available diamine (-)-sparteine as a chiral ligand and molecular oxygen as the stoichiometric oxidant. Mechanistic insights regar
Autor:
Raissa M. Trend, Peter O'Brien, Cedric Genet, David C. Ebner, Brian M. Stoltz, Matthew J. McGrath
Publikováno v:
ChemInform. 39
Rapid resolution: A new catalyst system for the oxidative kinetic resolution of secondary alcohols leads to dramatic rate increases. This system allows the use of a diamine to provide access to either enantiomer of a range of alcohols with good selec
Autor:
Raissa M. Trend, Cedric Genet, Matthew J. McGrath, Peter O'Brien, David C. Ebner, Brian M. Stoltz
Rapid resolution: A new catalyst system for the oxidative kinetic resolution of secondary alcohols leads to dramatic rate increases. This system allows the use of a diamine to provide access to either enantiomer of a range of alcohols with good selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ff20fc2ab372c1674afd11fc6c7fd13
https://resolver.caltech.edu/CaltechAUTHORS:20170215-152617371
https://resolver.caltech.edu/CaltechAUTHORS:20170215-152617371
Autor:
Raissa M. Trend, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 126(14)
A model for asymmetric induction in palladium-catalyzed aerobic oxidative kinetic resolution is described. The model is based on coordination complexes and general reactivity trends of the parent (sp)PdCl2 catalyst. The first example of a nonracemic
Publikováno v:
Angewandte Chemie (International ed. in English). 42(25)
A variety of Pd-catalyzed oxidative nucleophile/alkene cyclizations proceeds in excellent yield under simple aerobic conditions in nonpolar media (Pd catalyst, pyridine, and O_2 in toluene). Nucleophiles for these cyclizations include phenols, carbox
Autor:
Brian M. Stoltz, Matthew J. McGrath, Cédric Genet, Peter O'Brien, David C. Ebner, Raissa M. Trend
Publikováno v:
Synfacts. 2009:0121-0121