Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Kamalraj V. Rajendran"'
Publikováno v:
European Journal of Organic Chemistry. 2015:5959-5965
We report LiBH4 as a preferred, simple and effective reagent for reductive boronation of achiral and racemic chlorophosphonium salts (CPS) and for diastereomeric alkoxyphosphonium salts (DAPS), both of which are, in turn, easily generated from either
Publikováno v:
Chemical Communications. 51:16561-16564
A method is reported for the phosphoryl bond cleavage of O-alkyl phosphinates, phosphinothioates and certain phosphonamidates to furnish the corresponding P(III) borane adducts. The two-step procedure relies upon initial activation of the phosphoryl
Publikováno v:
Angewandte Chemie. 126:1937-1940
Synthetic routes that provide facile access to either enantiomeric form of a target compound are particularly valuable. The crystallization-free dual resolution of phosphine oxides that gives highly enantioenriched materials (up to 94 % ee) in excell
Publikováno v:
Tetrahedron Letters. 54:7009-7012
A wide selection of phosphine activators has been screened to improve the selection process in the asymmetric Appel reaction. Of the activators screened, hexachloroacetone (HCA) gave the highest selectivity with excellent yield, but at least one of i
Publikováno v:
Chemistry - A European Journal. 19:14210-14214
In contrast to tertiary phosphine oxides, the deoxygenation of aminophosphine oxides is effectively impossible due to the need to break the immensely strong and inert PO bond in the presence of a relatively weak and more reactive PN bond. This
Publikováno v:
European Journal of Organic Chemistry. 2012:2720-2723
An efficient one-pot synthesis has been developed of enantioenriched P-stereogenic phosphanes and phosphane boranes from the corresponding racemic phosphanes in excellent yield under asymmetric Appel conditions. The chiral auxiliary (menthol) can als
Publikováno v:
European Journal of Organic Chemistry. 2010:5642-5649
The effects of aryl ring substitution on the dynamic resolution of aryl(methyl)phenylphosphanes under asymmetric Appel reaction conditions have been studied. As expected, substitution at the ortho position strongly affects the degree ofstereoselectio
Publikováno v:
ChemInform. 46
We report LiBH4 as a preferred, simple and effective reagent for reductive boronation of achiral and racemic chlorophosphonium salts (CPS) and for diastereomeric alkoxyphosphonium salts (DAPS), both of which are, in turn, easily generated from either
Publikováno v:
Journal of the American Chemical Society. 137(29)
The dynamic resolution of tertiary phosphines and phosphine oxides was monitored by NMR spectroscopy. It was found that the stereoselectivity is set during the formation of the diastereomeric alkoxyphosphonium salts (DAPS), such that their initial di
Publikováno v:
ChemInform. 45
The method represents the first example for a dual chiral resolution of a racemic substrate being based on stereochemical bifurcation of an intermediate obtained with a single chiral auxiliary.