Results 201 to 210 of about 14,678 (255)
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
K. Abbaspour Tehrani, N. De Kimpe
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AbstractFor Abstract see ChemInform Abstract in Full Text.
K. Abbaspour Tehrani, N. De Kimpe
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Chemical Society Reviews, 2012
Formation of an imine--from an amine and an aldehyde--is a reversible reaction which operates under thermodynamic control such that the formation of kinetically competitive intermediates are, in the fullness of time, replaced by the thermodynamically most stable product(s).
Belowich, ME Belowich, Matthew E. +1 more
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Formation of an imine--from an amine and an aldehyde--is a reversible reaction which operates under thermodynamic control such that the formation of kinetically competitive intermediates are, in the fullness of time, replaced by the thermodynamically most stable product(s).
Belowich, ME Belowich, Matthew E. +1 more
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The Catalytic Acylcyanation of Imines
Chemistry – An Asian Journal, 2008AbstractThe catalytic acylcyanation of aldimines with acylcyanides and a direct three‐component variant involving the generation of an imine in situ have been developed. Furthermore, a highly enantioselective version has been established, culminating in the first organocatalytic asymmetric three‐component Strecker reaction.
Pan, S., List, B.
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Radical Aminomethylation of Imines
The Journal of Organic Chemistry, 2014Taking advantage of the high level of performance of N-alkoxycarbonyl-imines, we achieved the first example of addition of the aminomethyl radical to imine. The reaction efficiency depended on the structure of the radical precursor, whether it is an iodide or a xanthate, and an electron-withdrawing group on the nitrogen atom of the radical.
Shintaro, Fujii +5 more
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Enantioselective imine reduction catalyzed by imine reductases and artificial metalloenzymes
Org. Biomol. Chem., 2014Adding value to organic synthesis. Novel imine reductases enable the enantioselective reduction of imines to afford chiral amines. Likewise, novel bioinspired artificial metalloenzymes can perform the same reaction as well. Remarkable recent examples are herein discussed.
Daniela, Gamenara +1 more
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ChemInform Abstract: Isomerization of Imines in Platinum‐Imine Complexes.
ChemInform, 1987AbstractMultinuclear 1H, 13C and 195Pt NMR spectroscopy provides strong evidence for E‐Z isomerization of imine ligands coordinated to platinum(II).
A. M. AL‐SHALAAN +2 more
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Asymmetric Hydrogenation of Imines
2013Homogeneous catalytic asymmetric hydrogenation has evolved into a significantly useful methodology for the preparation of enantiopure compounds. Significant advances in asymmetric hydrogenation of imines have enabled a straightforward and powerful approach to various chiral amines.
Wei, Li, Xumu, Zhang
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1.3-additionen mit pyridin-imin, chinolin-imin, isochinolin-imin und phenanthridin-imin
Tetrahedron Letters, 1962Rolf Huisgen +2 more
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Acraldehyde Imine and 2‐Methylacraldehyde Imine
Angewandte Chemie International Edition in English, 1967B. Bogdanović, M. Velić
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