Xiaohua Liu focuses on Catalysis, Organic chemistry, Enantioselective synthesis, Medicinal chemistry and Scandium. His Catalysis study combines topics in areas such as Nitrile and Ene reaction. His research investigates the connection between Organic chemistry and topics such as Combinatorial chemistry that intersect with issues in Optically active.
His Stereocenter study, which is part of a larger body of work in Enantioselective synthesis, is frequently linked to Chemical synthesis, bridging the gap between disciplines. The concepts of his Medicinal chemistry study are interwoven with issues in Carboxylic acid, Thiol, Alcohol, Ring and Enantiopure drug. In his study, Aza-Diels–Alder reaction and Aldimine is inextricably linked to Trifluoromethanesulfonate, which falls within the broad field of Scandium.
Xiaohua Liu mostly deals with Catalysis, Enantioselective synthesis, Organic chemistry, Medicinal chemistry and Michael reaction. His Catalysis study combines topics from a wide range of disciplines, such as Yield, Combinatorial chemistry and Scandium. His Enantioselective synthesis research integrates issues from Catalytic cycle, Stereochemistry and Optically active.
He works mostly in the field of Catalytic cycle, limiting it down to topics relating to Bifunctional and, in certain cases, Cyanohydrin, as a part of the same area of interest. His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Amination, Nickel, Ring, Reactivity and Trifluoromethanesulfonate. The study incorporates disciplines such as Addition reaction and Amine gas treating in addition to Michael reaction.
His scientific interests lie mostly in Catalysis, Enantioselective synthesis, Medicinal chemistry, Organic chemistry and Yield. Xiaohua Liu combines subjects such as Scandium and Combinatorial chemistry with his study of Catalysis. His research integrates issues of Alkylation, Cycloaddition, Annulation, Phenacyl and Cascade reaction in his study of Enantioselective synthesis.
The Medicinal chemistry study combines topics in areas such as Friedel–Crafts reaction, Addition reaction and Magnesium. His Yield research incorporates elements of Nickel, Halogen, Ester derivatives, Diastereomer and Nucleophile. He studied Stereocenter and Stereochemistry that intersect with Succinimides, Axial chirality, Desymmetrization and Michael reaction.
His primary scientific interests are in Catalysis, Organic chemistry, Enantioselective synthesis, Yield and Medicinal chemistry. In Catalysis, Xiaohua Liu works on issues like Stereochemistry, which are connected to Stereocenter. His Enantioselective synthesis research includes themes of Scandium, Cascade reaction and Diol.
Xiaohua Liu has included themes like Diels–Alder reaction and Nickel in his Yield study. The concepts of his Medicinal chemistry study are interwoven with issues in Alcohol, Ester derivatives and Halogen. His Reaction conditions research includes elements of Optically active and Ene reaction.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
An N,N'-dioxide/In(OTf)3 catalyst for the asymmetric Hetero-Diels-Alder reaction between Danishefsky's dienes and aldehydes: application in the total synthesis of triketide
Zhipeng Yu;Xiaohua Liu;Zhenhua Dong;Mingsheng Xie.
Angewandte Chemie (2008)
Enantioselective Friedel–Crafts Alkylation of Indoles with Alkylidene Malonates Catalyzed by N,N′‐Dioxide–Scandium(III) Complexes: Asymmetric Synthesis of β‐Carbolines
Yanling Liu;Deju Shang;Xin Zhou;Xiaohua Liu.
Chemistry: A European Journal (2009)
Asymmetric Carbonyl-Ene Reaction Catalyzed by Chiral N,N′-Dioxide-Nickel(II) Complex: Remarkably Broad Substrate Scope
Ke Zheng;Jian Shi;Xiaohua Liu;Xiaoming Feng.
Journal of the American Chemical Society (2008)
Highly Enantioselective Aza-Henry Reaction of Ketoimines Catalyzed by Chiral N,N′-Dioxide−Copper(I) Complexes
Cheng Tan;Xiaohua Liu;Liwei Wang;Jun Wang.
Organic Letters (2008)
Asymmetric α-amination of 4-substituted pyrazolones catalyzed by a chiral Gd(OTf)3/N,N'-dioxide complex: highly enantioselective synthesis of 4-amino-5-pyrazolone derivatives.
Zhigang Yang;Zhen Wang;Sha Bai;Xiaohua Liu.
Organic Letters (2011)
Asymmetric Intramolecular Oxa‐Michael Addition of Activated α,β‐Unsaturated Ketones Catalyzed by a Chiral N,N′‐Dioxide Nickel(II) Complex: Highly Enantioselective Synthesis of Flavanones
Lijia Wang;Xiaohua Liu;Zhenhua Dong;Xuan Fu.
Angewandte Chemie (2008)
Catalytic asymmetric vinylogous Mannich-type (AVM) reaction of nonactivated α-angelica lactone.
Lin Zhou;Lili Lin;Jie Ji;Mingsheng Xie.
Organic Letters (2011)
Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(III)-complex catalyzed inverse-electron-demand hetero-Diels-Alder reaction.
Haipeng Hu;Yangbin Liu;Jing Guo;Lili Lin.
Chemical Communications (2015)
Highly Enantioselective Synthesis of 3‐Amino‐2‐oxindole Derivatives: Catalytic Asymmetric α‐Amination of 3‐Substituted 2‐Oxindoles with a Chiral Scandium Complex
Zhigang Yang;Zhen Wang;Sha Bai;Ke Shen.
Chemistry: A European Journal (2010)
Highly Z‐Selective Asymmetric Conjugate Addition of Alkynones with Pyrazol‐5‐ones Promoted by N,N′‐Dioxide–Metal Complexes
Zhen Wang;Zhenling Chen;Sha Bai;Wei Li.
Angewandte Chemie (2012)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: