Her primary areas of study are Catalysis, Enantioselective synthesis, Organic chemistry, Stereochemistry and Combinatorial chemistry. The study incorporates disciplines such as Ring, Ligand and Alkyl in addition to Catalysis. Her work deals with themes such as Yield, Nucleophile and Medicinal chemistry, which intersect with Enantioselective synthesis.
The concepts of her Yield study are interwoven with issues in Kinetic resolution and Concerted reaction. Reaction conditions, Scandium, Michael reaction, Indole test and Asymmetric induction are the core of her Organic chemistry study. Lili Lin has included themes like Bifunctional, Guanidine and Pyrazolin-5-Ones in her Michael reaction study.
Lili Lin mainly investigates Catalysis, Enantioselective synthesis, Organic chemistry, Medicinal chemistry and Combinatorial chemistry. Her work carried out in the field of Catalysis brings together such families of science as Yield, Stereochemistry and Scandium. Lili Lin works mostly in the field of Enantioselective synthesis, limiting it down to topics relating to Michael reaction and, in certain cases, Addition reaction.
Her Organic chemistry study is mostly concerned with Friedel–Crafts reaction, Aldol reaction, Diels–Alder reaction, Enantiomeric excess and Guanidine. Her Medicinal chemistry study integrates concerns from other disciplines, such as Amination, Aryl, Ring and Nucleophile. Lili Lin merges Combinatorial chemistry with Conjugate in her study.
Lili Lin focuses on Catalysis, Enantioselective synthesis, Medicinal chemistry, Organic chemistry and Combinatorial chemistry. She has researched Catalysis in several fields, including Yield and Stereochemistry. Her biological study spans a wide range of topics, including Guanidine, Amide and Efficient catalyst.
Her studies in Stereochemistry integrate themes in fields like Metal and Michael reaction. Lili Lin works mostly in the field of Enantioselective synthesis, limiting it down to concerns involving Catalytic cycle and, occasionally, Reaction mechanism. Her Medicinal chemistry research includes elements of Aldol reaction, Diels–Alder reaction, Ring and Silylation.
Lili Lin spends much of her time researching Catalysis, Enantioselective synthesis, Organic chemistry, Combinatorial chemistry and Medicinal chemistry. Her study in Catalysis is interdisciplinary in nature, drawing from both Yield, Chirality, Metal and Scandium. Her research integrates issues of Vicinal, Guanidine, Cycloaddition and Stereochemistry in her study of Enantioselective synthesis.
Her Combinatorial chemistry research is multidisciplinary, incorporating perspectives in Iminium, Zinc, Primary, Bimetallic strip and Electrophilic addition. Her studies deal with areas such as Crystal structure and Desymmetrization as well as Medicinal chemistry. Her Stereocenter research incorporates elements of Enantiomer and Diastereomer.
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Chiral N,N′-Dioxides: New Ligands and Organocatalysts for Catalytic Asymmetric Reactions
XiaoHua Liu;LiLi Lin;XiaoMing Feng.
Accounts of Chemical Research (2011)
Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action
Ke Shen;Xiaohua Liu;Lili Lin;Xiaoming Feng.
Chemical Science (2012)
Chiral N,N′-dioxide ligands: synthesis, coordination chemistry and asymmetric catalysis
Xiaohua Liu;Lili Lin;Xiaoming Feng.
Organic chemistry frontiers (2014)
Amide-based bifunctional organocatalysts in asymmetric reactions
Xiaohua Liu;Lili Lin;Xiaoming Feng.
Chemical Communications (2009)
Asymmetric three-component inverse electron-demand aza-Diels-Alder reaction: efficient synthesis of ring-fused tetrahydroquinolines.
M. Xie;X. Chen;Y. Zhu;B. Gao.
Angewandte Chemie (2010)
Asymmetric Cycloaddition and Cyclization Reactions Catalyzed by Chiral N,N′-Dioxide–Metal Complexes
Xiaohua Liu;Haifeng Zheng;Yong Xia;Lili Lin.
Accounts of Chemical Research (2017)
Catalytic Asymmetric Bromoamination of Chalcones: Highly Efficient Synthesis of Chiral α‐Bromo‐β‐Amino Ketone Derivatives
Yunfei Cai;Xiaohua Liu;Yonghai Hui;Jun Jiang.
Angewandte Chemie (2010)
Bifunctional Guanidine via an Amino Amide Skeleton for Asymmetric Michael Reactions of β‐Ketoesters with Nitroolefins: A Concise Synthesis of Bicyclic β‐Amino Acids
Zhipeng Yu;Xiaohua Liu;Lin Zhou;Lili Lin.
Angewandte Chemie (2009)
Chiral bisguanidine-catalyzed inverse-electron-demand hetero-Diels-Alder reaction of chalcones with azlactones.
Shunxi Dong;Xiaohua Liu;Xiaohong Chen;Fang Mei.
Journal of the American Chemical Society (2010)
Facile and efficient enantioselective hydroxyamination reaction: synthesis of 3-hydroxyamino-2-oxindoles using nitrosoarenes.
Ke Shen;Xiaohua Liu;Gang Wang;Lili Lin.
Angewandte Chemie (2011)
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