Results 331 to 340 of about 3,272,143 (363)
Enantioselective Total Synthesis of Batzelladine A [PDF]
AbstractFor Abstract see ChemInform Abstract in Full Text.
Aya Tanatani+4 more
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Angewandte Chemie, 2019
An efficient organocatalytic atroposelective three-component cascade reaction of 2,3-diketoesters, aromatic amines and 1,3-cyclohexanediones has been developed for the highly enantioselective synthesis of axially chiral N-arylindoles. The feature of this
Lei Wang, J. Zhong, Xufeng Lin
semanticscholar +1 more source
An efficient organocatalytic atroposelective three-component cascade reaction of 2,3-diketoesters, aromatic amines and 1,3-cyclohexanediones has been developed for the highly enantioselective synthesis of axially chiral N-arylindoles. The feature of this
Lei Wang, J. Zhong, Xufeng Lin
semanticscholar +1 more source
Enantioselective Synthesis of (−)-Pentalenene
Organic Letters, 2007A short, enantioselective synthesis of (-)-pentalenene is described. Catalytic enantioselective cyclopropenation with (R,R)-Rh2(OAc)(DPTI)3 was used to set the absolute stereochemistry, and an intramolecular Pauson-Khand reaction of the resulting cyclopropenyne was used to establish the quaternary center.
Mahesh K. Pallerla, Joseph M. Fox
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Angewandte Chemie, 2019
The discovery of proper ligands to simultaneously modulate the reactivity and effectively control the stereoselectivity is a central topic in the field of enantioselective C-H activation.
Jun Luo+9 more
semanticscholar +1 more source
The discovery of proper ligands to simultaneously modulate the reactivity and effectively control the stereoselectivity is a central topic in the field of enantioselective C-H activation.
Jun Luo+9 more
semanticscholar +1 more source
Enantioselective Synthesis of Silanol
Journal of the American Chemical Society, 2008An enantioselective nucleophilic substitution reaction of achiral dialkoxysilane has been developed. The reaction proceeds with efficient stereocontrol on the silicon chirality center to give the enantioenriched silyl ether, which can be converted to the silanol without loss of enantiopurity.
Junko Takada+3 more
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Enantioselective Synthesis of (−)-Dysiherbaine
Organic Letters, 2015Dysiherbaine, a natural product isolated from the Marine sponge Dysidea herbacea, has been shown to be a selective agonist of non-NMDA type glutamate receptors, kainate receptors. An enantioselective synthesis of dysiherbaine is reported. Metathesis of the diene followed by conversion of the resulting alkene to the amino alcohol and addition of the ...
Joon Hyung Cho+3 more
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Angewandte Chemie, 2019
The first enantioselective Satoh-Miura-type reaction is reported. A variety of C-N axially chiral N-aryloxindoles have been enantioselectively synthesized by an asymmetric rhodium-catalyzed dual C-H activation reaction of N-aryloxindoles and alkynes ...
Honghe Li+5 more
semanticscholar +1 more source
The first enantioselective Satoh-Miura-type reaction is reported. A variety of C-N axially chiral N-aryloxindoles have been enantioselectively synthesized by an asymmetric rhodium-catalyzed dual C-H activation reaction of N-aryloxindoles and alkynes ...
Honghe Li+5 more
semanticscholar +1 more source
Angewandte Chemie, 2019
A cooperative Cu/Pd-catalyzed enantioselective synthesis of multisubstituted allenes is established. By employing chiral sulfoxide phosphine (SOP)/Cu and PdCl2 (dppf) complexes as catalysts, the 1,4-arylboration of 1,3-enynes provides an efficient ...
Yangzhen Liao+7 more
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A cooperative Cu/Pd-catalyzed enantioselective synthesis of multisubstituted allenes is established. By employing chiral sulfoxide phosphine (SOP)/Cu and PdCl2 (dppf) complexes as catalysts, the 1,4-arylboration of 1,3-enynes provides an efficient ...
Yangzhen Liao+7 more
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An Enantioselective Synthesis of Tarchonanthuslactone
The Journal of Organic Chemistry, 2002An enantioselective synthesis of tarchonanthuslactone has been achieved in eight steps from ethyl sorbate. The asymmetry of the route was introduced via a Sharpless asymmetric dihydroxylation allowing access to either enantiomer. The synthesis utilizes a palladium-catalyzed reduction and a diastereoselective base-catalyzed acetal formation as the key ...
Sarah D Garaas+2 more
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Angewandte Chemie, 2018
The combination of photoredox and enzymatic catalysis for the direct asymmetric one-pot synthesis of 2,2-disubstituted indol-3-ones from 2-arylindoles through concurrent oxidization and alkylation reactions is described.
Xuan Ding+3 more
semanticscholar +1 more source
The combination of photoredox and enzymatic catalysis for the direct asymmetric one-pot synthesis of 2,2-disubstituted indol-3-ones from 2-arylindoles through concurrent oxidization and alkylation reactions is described.
Xuan Ding+3 more
semanticscholar +1 more source