Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Natsuka Higashi"'
Publikováno v:
Organometallics. 20:4542-4553
A new P-chirogenic diphosphine, (S,S)-α,α‘-bis(tert-butylmethylphosphino)-o-xylene (1), was synthesized in two steps from optically active secondary phosphine-borane 4 via the corresponding diphosphine-borane 3. The Rh(I) complex (2) of 1 was cha
Publikováno v:
Journal of the American Chemical Society. 123:5268-5276
The asymmetric hydrogenation of aryl- and alkyl-substituted enamides catalyzed by Rh-BisP complex affords optically active amides with very high ee values. The Rh-MiniPHOS catalyst gives somewhat less satisfactory results. Hydrogenation of the aryl-s
Autor:
Ilya D. Gridnev, Natsuka Higashi, Yoshinori Yamanoi, Tsuneo Imamoto, Masaya Yasutake, Hideyuki Tsuruta
Publikováno v:
Advanced Synthesis & Catalysis. 343:118-136
A new class of chiral C2-symmetric bis(trialkyl)phosphine ligands has been prepared and used in Rh(I)-catalyzed asymmetric hydrogenation reactions. The ligands, 1,2-bis(alkylmethylphosphino)ethanes 1a-g(abbreviated as BisP*, alkyl = t-butyl, 1-adaman
Publikováno v:
Journal of the American Chemical Society. 122:7183-7194
The mechanism of asymmetric hydrogenation catalyzed by a new effective catalyst, viz., a rhodium complex of (S,S)-1,2-bis(tert-butylmethylphosphino)ethane (BisP*), has been studied by multinuclear NMR. Hydrogenation of the precatalyst [Rh(BisP*)(nbd)
Autor:
Michiko Kobayashi, Shigeru Watanabe, Natsuka Higashi, Katsuhira Yoshida, Yoshiyuki Takata, Kaori Hamanaka
Publikováno v:
Tetrahedron Letters. 41:4583-4586
An induced-fit type Ru(II) receptor 1 has been synthesized in which, upon approach of dicarboxylates, a highly flexible tetraamide binding site is organized to complement their chemical structures. Stereoselective optical sensing has been demonstrate
Autor:
Tsuneo Imamoto, Hideyuki Tsuruta, Masaya Yasutake, Yoshinori Yamanoi, Ilya D. Gridnev, Natsuka Higashi
Publikováno v:
ChemInform. 32
A new class of chiral C2-symmetric bis(trialkyl)phosphine ligands has been prepared and used in Rh(I)-catalyzed asymmetric hydrogenation reactions. The ligands, 1,2-bis(alkylmethylphosphino)ethanes 1a-g(abbreviated as BisP*, alkyl = t-butyl, 1-adaman
Publikováno v:
ChemInform. 32
Excellent enantioselectivities up to 99.7% were achieved in the hydrogenation of (E)-β-(acylamino)acrylates by the use of Rh(I)-complexes of electron-rich diphosphines, t-Bu-BisP* and t-Bu-MiniPHOS. Low-temperature NMR experiments testify that monoh
Publikováno v:
ChemInform. 32
The asymmetric hydrogenation of aryl- and alkyl-substituted enamides catalyzed by Rh-BisP* complex affords optically active amides with very high ee values. The Rh-MiniPHOS catalyst gives somewhat less satisfactory results. Hydrogenation of the aryl-
Publikováno v:
Organic letters. 3(11)
Excellent enantioselectivities up to 99.7% were achieved in the hydrogenation of (E)-beta-(acylamino)acrylates by the use of Rh(I)-complexes of electron-rich diphosphines, t-Bu-BisP and t-Bu-MiniPHOS. Low-temperature NMR experiments testify that mono
Publikováno v:
Journal of the American Chemical Society. 123:4631-4632