His scientific interests lie mostly in Enantioselective synthesis, Catalysis, Organic chemistry, Stereocenter and Stereochemistry. His Enantioselective synthesis research includes elements of Indole test and Chirality. The concepts of his Catalysis study are interwoven with issues in Yield, Combinatorial chemistry and Isatin.
In the field of Organic chemistry, his study on Cascade reaction, Brønsted–Lowry acid–base theory and Amine gas treating overlaps with subjects such as Component. His studies deal with areas such as Phosphoric acid, Indoline and Povarov reaction as well as Stereocenter. His Stereochemistry research is multidisciplinary, incorporating elements of Stereoselectivity, Molecule, Stereoisomerism and Azomethine ylide.
Feng Shi mostly deals with Catalysis, Organic chemistry, Combinatorial chemistry, Enantioselective synthesis and Microwave irradiation. His work carried out in the field of Catalysis brings together such families of science as Yield, Medicinal chemistry, Indole test and Phosphoric acid. His work on Dimedone, Aldehyde, One-pot synthesis and Tetronic acid is typically connected to Ammonium acetate as part of general Organic chemistry study, connecting several disciplines of science.
Feng Shi has researched Combinatorial chemistry in several fields, including Cascade reaction, Electrophile, Solvent and Microwave assisted. His Enantioselective synthesis research is multidisciplinary, relying on both Isatin and Stereochemistry. He combines subjects such as Oxindole and Povarov reaction with his study of Stereocenter.
Feng Shi focuses on Catalysis, Combinatorial chemistry, Enantioselective synthesis, Indole test and Yield. His Catalysis study is concerned with the larger field of Organic chemistry. His work on Phosphine as part of general Organic chemistry study is frequently connected to Tryptamines, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
The Combinatorial chemistry study combines topics in areas such as Electrophile, Oxindole, Ring and Phosphoric acid. As a part of the same scientific family, he mostly works in the field of Enantioselective synthesis, focusing on Organic synthesis and, on occasion, Isatin. Feng Shi has included themes like Reagent, O quinones, Chiral amine and Trifluoroacetic acid in his Yield study.
Catalysis, Combinatorial chemistry, Enantioselective synthesis, Para-quinone and Axial symmetry are his primary areas of study. In his study, Alkyl is inextricably linked to Medicinal chemistry, which falls within the broad field of Catalysis. His Combinatorial chemistry study integrates concerns from other disciplines, such as In situ, Isatin, Cycloaddition, Phosphoric acid and Oxindole.
Feng Shi is studying Organocatalysis, which is a component of Enantioselective synthesis. His Para-quinone research includes themes of Aryne and Xanthene. His research on Metal concerns the broader Organic chemistry.
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Brønsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles
Jie Yu;Feng Shi;Liu-Zhu Gong.
Accounts of Chemical Research (2011)
Catalytic asymmetric synthesis of spirooxindoles: recent developments
Guang-Jian Mei;Feng Shi.
Chemical Communications (2018)
Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach.
Yu-Chen Zhang;Fei Jiang;Feng Shi.
Accounts of Chemical Research (2020)
Design and Enantioselective Construction of Axially Chiral Naphthyl‐Indole Skeletons
Hong-Hao Zhang;Cong-Shuai Wang;Can Li;Guang-Jian Mei.
Angewandte Chemie (2017)
Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles
Jia-Jia Zhao;Si-Bing Sun;Sai-Huan He;Qiong Wu.
Angewandte Chemie (2015)
Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′-Bisindole Skeletons
Chun Ma;Fei Jiang;Feng-Tao Sheng;Yinchun Jiao.
Angewandte Chemie (2019)
Scaffold‐Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin‐3,2′‐oxindoles] with Structural Diversity through Catalytic Isatin‐Derived 1,3‐Dipolar Cycloadditions
Feng Shi;Zhong‐Lin Tao;Shi‐Wei Luo;Shu‐Jiang Tu.
Chemistry: A European Journal (2012)
A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2′-quinoline] Scaffold
Feng Shi;Gui-Juan Xing;Ren-Yi Zhu;Wei Tan.
Organic Letters (2013)
Organocatalytic Asymmetric Arylative Dearomatization of 2,3‐Disubstituted Indoles Enabled by Tandem Reactions
Yu-Chen Zhang;Jia-Jia Zhao;Fei Jiang;Si-Bing Sun.
Angewandte Chemie (2014)
Diastereo- and Enantioselective Construction of 3,3'-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions.
Wei Dai;Xiao-Li Jiang;Qiong Wu;Feng Shi.
Journal of Organic Chemistry (2015)
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