World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
65
Citations
12445
World Ranking
7814
National Ranking
55

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Aldehyde

Yonggui Robin Chi mostly deals with Catalysis, Organic chemistry, Carbene, Enantioselective synthesis and Organocatalysis. His work investigates the relationship between Catalysis and topics such as Combinatorial chemistry that intersect with problems in Single bond. Yonggui Robin Chi has researched Carbene in several fields, including Cycloaddition, Surface modification, Stereochemistry, Trifluoromethyl and Nucleophile.

Brønsted–Lowry acid–base theory is closely connected to Electrophile in his research, which is encompassed under the umbrella topic of Nucleophile. His Enantioselective synthesis research focuses on subjects like Isatin, which are linked to Steric effects, Benzoin and Chemoselectivity. The various areas that Yonggui Robin Chi examines in his Organocatalysis study include Aldehyde, Michael reaction, HOMO/LUMO, Ketone and Enone.

His most cited work include:

  • A family of metal-organic frameworks exhibiting size-selective catalysis with encapsulated noble-metal nanoparticles. (257 citations)
  • Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis. (243 citations)
  • β-Carbon activation of saturated carboxylic esters through N -heterocyclic carbene organocatalysis (168 citations)

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

His main research concerns Catalysis, Carbene, Enantioselective synthesis, Combinatorial chemistry and Organic chemistry. In Catalysis, Yonggui Robin Chi works on issues like Molecule, which are connected to Lactone and Functional group. The Carbene study combines topics in areas such as Surface modification, Organocatalysis, Carbon and Medicinal chemistry.

His work carried out in the field of Enantioselective synthesis brings together such families of science as Iminium, Nucleophilic addition, Annulation and Imine. His Combinatorial chemistry study also includes fields such as

  • Kinetic resolution and related Acylation,
  • Heteroatom most often made with reference to Moiety. His work on Electrophile, Ketone, Stereoisomerism and Diels alder as part of general Organic chemistry study is frequently linked to Oxidative phosphorylation, therefore connecting diverse disciplines of science.

He most often published in these fields:

  • Catalysis (119.48%)
  • Carbene (106.06%)
  • Enantioselective synthesis (57.58%)

What were the highlights of his more recent work (between 2019-2021)?

  • Catalysis (119.48%)
  • Carbene (106.06%)
  • Combinatorial chemistry (63.64%)

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

His primary scientific interests are in Catalysis, Carbene, Combinatorial chemistry, Enantioselective synthesis and Medicinal chemistry. His Catalysis research includes elements of Steric effects and Polymer chemistry. Yonggui Robin Chi has included themes like Organocatalysis, Cycloaddition, Annulation and Nucleophilic addition in his Carbene study.

His Combinatorial chemistry study combines topics from a wide range of disciplines, such as Kinetic resolution, Molecule, Chirality, Addition reaction and Stereoselectivity. His Enantioselective synthesis research is multidisciplinary, incorporating elements of Lactam, Heteroatom, Aldol reaction, Allene and Aryl. His work in the fields of Organic chemistry, such as Amination, overlaps with other areas such as Component.

Between 2019 and 2021, his most popular works were:

  • Prediction of NHC-catalyzed chemoselective functionalizations of carbonyl compounds: a general mechanistic map (15 citations)
  • A Glycosylated Cationic Block Poly(β-peptide) Reverses Intrinsic Antibiotic Resistance in All ESKAPE Gram-Negative Bacteria. (14 citations)
  • Gold and Carbene Relay Catalytic Enantioselective Cycloisomerization/Cyclization Reactions of Ynamides and Enals (13 citations)

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

  • Organic chemistry
  • Catalysis
  • Aldehyde

Yonggui Robin Chi spends much of his time researching Combinatorial chemistry, Carbene, Catalysis, Enantioselective synthesis and Electrophile. His Combinatorial chemistry study integrates concerns from other disciplines, such as Indoline, Cascade reaction, Palladium and Stereoselectivity. His Carbene study incorporates themes from Organocatalysis, Reactive intermediate, Nucleophile and Homogeneous catalysis.

Catalysis and Rapid access are two areas of study in which he engages in interdisciplinary work. His biological study spans a wide range of topics, including Lactam, Transition metal, Cycloisomerization, Metal and Bicyclic molecule. His Electrophile study necessitates a more in-depth grasp of Organic chemistry.

Best Publications

  • A family of metal-organic frameworks exhibiting size-selective catalysis with encapsulated noble-metal nanoparticles.

    Weina Zhang;Guang Lu;Chenlong Cui;Yayuan Liu

  • Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis.

    Junming Mo;Xingkuan Chen;Yonggui Robin Chi

  • One-pot multi-component asymmetric cascade reactions catalyzed by soluble star polymers with highly branched non-interpenetrating catalytic cores.

    Yonggui Chi;Steven T Scroggins;Jean M J Fréchet

  • N‐Heterocyclic Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates

    Xingkuan Chen;Hongling Wang;Zhichao Jin;Yonggui Robin Chi;Yonggui Robin Chi

  • β-Carbon activation of saturated carboxylic esters through N -heterocyclic carbene organocatalysis

    Zhenqian Fu;Jianfeng Xu;Tingshun Zhu;Wendy Wen Yi Leong

  • N-heterocyclic carbene-catalyzed [3+4] cycloaddition and kinetic resolution of azomethine imines

    Ming Wang;Zhijian Huang;Jianfeng Xu;Yonggui Robin Chi

  • NHC Organocatalytic Formal LUMO Activation of α,β‐Unsaturated Esters for Reaction with Enamides

    Jiajia Cheng;Zhijian Huang;Yonggui Robin Chi

  • Functionalization of Benzylic C(sp3)H Bonds of Heteroaryl Aldehydes through N‐Heterocyclic Carbene Organocatalysis

    Xingkuan Chen;Song Yang;Bao-An Song;Yonggui Robin Chi

  • Carbene-Catalyzed Asymmetric Construction of Atropisomers.

    Runjiang Song;Yongtao Xie;Zhichao Jin;Yonggui Robin Chi

  • Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts.

    Lin Hao;Yu Du;Hui Lv;Xingkuan Chen

  • Highly enantioselective addition of enals to isatin-derived ketimines catalyzed by N-heterocyclic carbenes: synthesis of spirocyclic γ-lactams.

    Hui Lv;Bhoopendra Tiwari;Junming Mo;Chong Xing

  • Enantioselective Organocatalytic Aminomethylation of Aldehydes: A Role for Ionic Interactions and Efficient Access to β2-Amino Acids

    Yonggui Chi;Samuel H. Gellman

  • Benzene construction via organocatalytic formal [3+3] cycloaddition reaction

    Tingshun Zhu;Pengcheng Zheng;Chengli Mou;Song Yang

  • N-heterocyclic carbene-catalyzed radical reactions for highly enantioselective β-hydroxylation of enals.

    Yuexia Zhang;Yu Du;Zhijian Huang;Jianfeng Xu

  • Enantioselective Organocatalytic Michael Addition of Aldehydes to Nitroethylene: Efficient Access to γ2-Amino Acids

    Yonggui Chi;Li Guo;Nathan A. Kopf;Samuel H. Gellman

  • Stereospecific Synthesis of Conformationally Constrained γ-Amino Acids: New Foldamer Building Blocks That Support Helical Secondary Structure

    Li Guo;Yonggui Chi;Aaron M. Almeida;Ilia A. Guzei

  • Enantioselective Oxidative Cross-Dehydrogenative Coupling of Tertiary Amines to Aldehydes**

    Junmin Zhang;Bhoopendra Tiwari;Chong Xing;Xingkuan Chen

  • Organocatalytic Enantioselective γ-Aminoalkylation of Unsaturated Ester: Access to Pipecolic Acid Derivatives

    Jianfeng Xu;Zhichao Jin;Yonggui Robin Chi

  • Direct β‐Activation of Saturated Aldehydes to Formal Michael Acceptors through Oxidative NHC Catalysis

    Junming Mo;Liang Shen;Yonggui Robin Chi

  • Access to P-Stereogenic Phosphinates via N-Heterocyclic Carbene-Catalyzed Desymmetrization of Bisphenols

    Zhijian Huang;Xuan Huang;Baosheng Li;Chengli Mou

  • Enantioselective Organocatalytic Michael Additions of Aldehydes to Enones

    T. J. Peelen;Y. Chi;S. H. Gellman

Frequent Co-Authors

Song Yang
Song Yang Guizhou University
Baoan Song
Baoan Song Guizhou University
Bin Liu
Bin Liu National University of Singapore
Richard D. Webster
Richard D. Webster Nanyang Technological University
Jun Sun
Jun Sun Singapore Management University
Rakesh Ganguly
Rakesh Ganguly Nanyang Technological University
Fengwei Huo
Fengwei Huo Nanjing Tech University
Yun-Dong Wu
Yun-Dong Wu Peking University
Mary B. Chan-Park
Mary B. Chan-Park Nanyang Technological University
Guillermo C. Bazan
Guillermo C. Bazan National University of Singapore

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