D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 61 Citations 10,781 201 World Ranking 6146 National Ranking 862

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

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.

His most cited work include:

  • Brønsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles (593 citations)
  • Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles (195 citations)
  • Scaffold‐Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin‐3,2′‐oxindoles] with Structural Diversity through Catalytic Isatin‐Derived 1,3‐Dipolar Cycloadditions (161 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Catalysis (53.31%)
  • Organic chemistry (40.06%)
  • Combinatorial chemistry (40.06%)

What were the highlights of his more recent work (between 2017-2021)?

  • Catalysis (53.31%)
  • Combinatorial chemistry (40.06%)
  • Enantioselective synthesis (35.54%)

In recent papers he was focusing on the following fields of study:

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.

Between 2017 and 2021, his most popular works were:

  • Catalytic asymmetric synthesis of spirooxindoles: recent developments (154 citations)
  • Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach (89 citations)
  • Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′‐Bisindole Skeletons (88 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Catalysis
  • Alkene

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.

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.

Best Publications

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)

1085 Citations

Catalytic asymmetric synthesis of spirooxindoles: recent developments

Guang-Jian Mei;Feng Shi.
Chemical Communications (2018)

389 Citations

Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach.

Yu-Chen Zhang;Fei Jiang;Feng Shi.
Accounts of Chemical Research (2020)

311 Citations

Design and Enantioselective Construction of Axially Chiral Naphthyl‐Indole Skeletons

Hong-Hao Zhang;Cong-Shuai Wang;Can Li;Guang-Jian Mei.
Angewandte Chemie (2017)

285 Citations

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)

269 Citations

Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′-Bisindole Skeletons

Chun Ma;Fei Jiang;Feng-Tao Sheng;Yinchun Jiao.
Angewandte Chemie (2019)

252 Citations

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)

244 Citations

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)

238 Citations

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)

235 Citations

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)

222 Citations

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