His main research concerns Organic chemistry, Catalysis, Combinatorial chemistry, Hydroamination and Enantioselective synthesis. His Catalysis research is multidisciplinary, incorporating perspectives in Substrate and Copper. His research investigates the connection between Substrate and topics such as Chemoselectivity that intersect with problems in Intramolecular force and Trifluoromethyl.
His Combinatorial chemistry research focuses on subjects like Functional group, which are linked to Reaction conditions. His study explores the link between Hydroamination and topics such as Microwave assisted that cross with problems in Microwave irradiation, Organic reaction, Isomerization and Phosphine. His Enantioselective synthesis study combines topics in areas such as Brønsted–Lowry acid–base theory and Stereoselectivity.
Xin-Yuan Liu focuses on Catalysis, Combinatorial chemistry, Organic chemistry, Enantioselective synthesis and Intramolecular force. His Catalysis study incorporates themes from Medicinal chemistry and Phosphoric acid. He has researched Combinatorial chemistry in several fields, including Aryl, Alkyl, Substrate and Reaction conditions.
His Enantioselective synthesis research is multidisciplinary, relying on both Brønsted–Lowry acid–base theory, Optically active and Aldehyde. His studies in Intramolecular force integrate themes in fields like Amination and Michael reaction. His Hydroamination research includes themes of Photochemistry and Microwave assisted.
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Alkyl, Copper and Enantioselective synthesis. His studies deal with areas such as Photochemistry, Racemization and Intermolecular force as well as Catalysis. Xin-Yuan Liu interconnects Aryl, Radical, Alkene and Stereocenter in the investigation of issues within Combinatorial chemistry.
The study incorporates disciplines such as Oxidative addition, Alkylation and Substrate in addition to Copper. His Enantioselective synthesis research includes elements of Amination, Intramolecular force and Chemoselectivity. His research on Amination concerns the broader Organic chemistry.
His primary areas of study are Combinatorial chemistry, Catalysis, Enantioselective synthesis, Alkyl and Copper. The Combinatorial chemistry study combines topics in areas such as Denticity, Organic synthesis, Asymmetric induction, Radical and Chemoselectivity. Catalysis is a subfield of Organic chemistry that Xin-Yuan Liu explores.
His work in the fields of Enantioselective synthesis, such as Enantiomeric excess, intersects with other areas such as Surface modification. His biological study spans a wide range of topics, including Side reaction, Glaser coupling, Stereocenter and Cinchona. His Copper research is multidisciplinary, incorporating elements of Alkene, Silylation and Organic molecules.
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.
Synthesis of Substituted 1,2-Dihydroquinolines and Quinolines from Aromatic Amines and Alkynes by Gold(I)-Catalyzed Tandem Hydroamination−Hydroarylation under Microwave-Assisted Conditions
Xin-Yuan Liu;Pan Ding;Jie-Sheng Huang;Chi-Ming Che.
Organic Letters (2007)
Phosphine gold(I)-catalyzed hydroamination of alkenes under thermal and microwave-assisted conditions.
Xin-Yuan Liu;Cheng-Hui Li;Chi-Ming Che.
Organic Letters (2006)
Highly enantioselective synthesis of chiral secondary amines by gold(I)/chiral Brønsted acid catalyzed tandem intermolecular hydroamination and transfer hydrogenation reactions.
Xin-Yuan Liu;Chi-Ming Che.
Organic Letters (2009)
Recent advances in copper-catalysed radical-involved asymmetric 1,2-difunctionalization of alkenes
Zhong-Liang Li;Gui-Chun Fang;Qiang-Shuai Gu;Xin-Yuan Liu.
Chemical Society Reviews (2020)
Atroposelective Synthesis of Axially Chiral Biaryldiols via Organocatalytic Arylation of 2-Naphthols.
Ye-Hui Chen;Dao-Juan Cheng;Jian Zhang;Yong Wang.
Journal of the American Chemical Society (2015)
A Dual-Catalytic Strategy To Direct Asymmetric Radical Aminotrifluoromethylation of Alkenes
Jin-Shun Lin;Xiao-Yang Dong;Tao-Tao Li;Na-Chuan Jiang.
Journal of the American Chemical Society (2016)
Enantioselective C-H bond functionalization triggered by radical trifluoromethylation of unactivated alkene.
Peng Yu;Jin-Shun Lin;Lei Li;Sheng-Cai Zheng.
Angewandte Chemie (2014)
A Highly Efficient and Selective AuI‐Catalyzed Tandem Synthesis of Diversely Substituted Pyrrolo[1,2‐a]quinolines in Aqueous Media
Xin-Yuan Liu;Chi-Ming Che.
Angewandte Chemie (2008)
Metal-Free Direct Intramolecular Carbotrifluoromethylation of Alkenes to Functionalized Trifluoromethyl Azaheterocycles
Lei Li;Min Deng;Sheng-Cai Zheng;Ya-Ping Xiong.
Organic Letters (2014)
Radical-Mediated 1,2-Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium-Sized Rings
Zhong-Liang Li;Zhong-Liang Li;Xiao-Hua Li;Na Wang;Ning-Yuan Yang.
Angewandte Chemie (2016)
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: