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Catalytic Asymmetric Arylation of α-Aryl-α-diazoacetates with Aniline Derivatives.
- B. Xu, Mao-lin Li, Xiao-Dong Zuo, S. Zhu, Q. Zhou
- Chemistry, Medicine
- Journal of the American Chemical Society
- 6 July 2015
The asymmetric arylation of diazo compounds with aniline derivatives cooperatively catalyzed by an achiral dirhodium complex and a chiral spiro phosphoric acid is reported. The reaction provides a… Expand
Enantioselective N-H insertion reaction of α-aryl α-diazoketones: an efficient route to chiral α-aminoketones.
- B. Xu, S. Zhu, Xiao-Dong Zuo, Zhi-chao Zhang, Q. Zhou
- Chemistry, Medicine
- Angewandte Chemie
- 7 April 2014
A highly enantioselective NH insertion reaction of α-diazoketones was developed by using cooperative catalysis by dirhodium(II) carboxylates and chiral spiro phosphoric acids. The insertion reaction… Expand
Bioinspired enantioselective synthesis of crinine-type alkaloids via iridium-catalyzed asymmetric hydrogenation of enones† †Electronic supplementary information (ESI) available. See DOI:…
A bioinspired enantioselective synthesis of crinine-type alkaloids was developed by iridium-catalyzed asymmetric hydrogenation of enones, providing 24 crinine-type alkaloids and 8 analogues with high… Expand
Catalytic Asymmetric Arylation of α‐Aryl‐α‐diazoacetates with Aniline Derivatives.
Asymmetric Total Synthesis of Gracilamine and Determination of Its Absolute Configuration.
(+)-Gracilamine, a biologically attractive and structurally unique pentacyclic Amaryllidaceae alkaloid, was biomimetically synthesized in 11 linear steps in 9.9% overall yield from the known racemic… Expand
Molten Salt Synthesis of High-Performance, Nanostructured La0.6Sr0.4FeO3−δ Oxygen Electrode of a Reversible Solid Oxide Cell
Nanoscale perovskite oxides with enhanced electrocatalytic activities have been widely used as oxygen electrodes of reversible solid oxide cells (RSOC). Here, La0.6Sr0.4FeO3−δ (LSF) nanoscale powder… Expand
Enantioselective N—H Insertion Reaction of α‐Aryl α‐Diazoketones: An Efficient Route to Chiral α‐Aminoketones.
This is the first asymmetric N—H insertion of α-diazoketones giving α-aminoketones in good yields and with high enantioselectivities.