Leaderboards/Cyclopropane Reaction Mechanisms

Cyclopropane Reaction Mechanisms

Last updated July 7, 2026

Rising Stars

New and hot

Rising Stars Researchers

1
You‐Jie Yu
University of Science and Technology of China
2
Soumitra Agasti
University of Manchester
3
Kushal Dhake
University of Victoria
4
Wan‐Chen Cindy Lee
Boston College
5
Bao‐Gui Cai
Anhui University
6
Jakub Durka
Institute of Organic Chemistry
7
Satyajit Roy
The University of Texas at Dallas
8
Yangyang Yang
The University of Texas Southwestern Medical Center
9
Shao‐Qian Yang
Chinese Academy of Sciences
10
Patrick W. Antoni
Heidelberg University

Rising Stars Papers

1
Diastereoselective dearomative cycloaddition of bicyclobutanes with pyridinium ylides: a modular approach to multisubstituted azabicyclo[3.1.1]heptanes
Chemical Communications|2024
23 cit.
2
Stereodivergent Synthesis of Pyridyl Cyclopropanes via Enzymatic Activation of Pyridotriazoles
Journal of the American Chemical Society|2024
20 cit.
3
Asymmetric C–H Amination via Fe(III)-Metalloradical Catalysis Featuring α-Fe(IV)-Aminyl Radicals as Key Intermediates
Journal of the American Chemical Society|2025
18 cit.
4
Asymmetric radical aziridination of alkenes
Trends in Chemistry|2024
9 cit.
5
Metalloradical Catalysis: General Approach for Controlling Reactivity and Selectivity of Homolytic Radical Reactions
Angewandte Chemie|2024
8 cit.
6
Beyond single pathways: synergistic SET–EnT pathways in visible-light photochemistry
Chemical Society Reviews|2026
8 cit.
7
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Angewandte Chemie International Edition|2024
6 cit.
8
<i>N</i>-Aryl/heteroaryl oxaziridines: from photochemical synthesis to reactivity investigation in heteroatom transfer reactions
Organic Chemistry Frontiers|2024
4 cit.
9
Sequential C–H Aroylation and Formal [4 + 2] Cycloaddition of Naphthalenes with Aroylfluorides and Styrenes
ACS Catalysis|2025
4 cit.
10
Regioselective Electrochemical Borylation of Oxygenated Allylic Electrophiles: Method Development and Synthetic Applications
ACS Central Science|2025
4 cit.

Emerging Leaders

Gaining momentum

Emerging Leaders Researchers

1
Jian‐Jun Feng
Jimei University
2
Fa‐Guang Zhang
Tianjin University
3
Lu Liu
Shihezi University
4
Osvaldo Gutiérrez
University of California, Los Angeles
5
Mengchun Ye
Nankai University
6
Shi‐Liang Shi
Shanghai Institute of Organic Chemistry
7
Xiao‐Song Xue
Shanghai Institute of Organic Chemistry
8
Fanke Meng
Chinese Academy of Sciences
9
Andrew McNally
Princeton University
10
Jin Xie
China Pharmaceutical University

Emerging Leaders Papers

1
Halogenation of the 3-position of pyridines through Zincke imine intermediates
Science|2022
170 cit.
2
Silver‐Catalyzed Dearomative [2π+2σ] Cycloadditions of Indoles with Bicyclobutanes: Access to Indoline Fused Bicyclo[2.1.1]hexanes**
Angewandte Chemie International Edition|2023
158 cit.
3
Highly selective synthesis of all-carbon tetrasubstituted alkenes by deoxygenative alkenylation of carboxylic acids
Nature Communications|2022
134 cit.
4
Palladium-Catalyzed Ligand-Controlled Switchable Hetero-(5 + 3)/Enantioselective [2σ+2σ] Cycloadditions of Bicyclobutanes with Vinyl Oxiranes
Journal of the American Chemical Society|2024
134 cit.
5
Photoinduced gold-catalyzed divergent dechloroalkylation of gem-dichloroalkanes
Nature Catalysis|2022
120 cit.
6
Cobalt-Catalyzed Sequential Site- and Stereoselective Hydrosilylation of 1,3- and 1,4-Enynes
Journal of the American Chemical Society|2022
112 cit.
7
Switching between the [2π+2σ] and Hetero‐[4π+2σ] Cycloaddition Reactivity of Bicyclobutanes with Lewis Acid Catalysts Enables the Synthesis of Spirocycles and Bridged Heterocycles
Angewandte Chemie International Edition|2024
106 cit.
8
Enantio- and Regioselective Ni-Catalyzed <i>para</i>-C–H Alkylation of Pyridines with Styrenes via Intermolecular Hydroarylation
Journal of the American Chemical Society|2022
102 cit.
9
Enantioselective formal (3 + 3) cycloaddition of bicyclobutanes with nitrones enabled by asymmetric Lewis acid catalysis
Nature Communications|2024
86 cit.
10
Decarboxylative tandem C-N coupling with nitroarenes via SH2 mechanism
Nature Communications|2022
84 cit.

Current Senior Leaders

Established & currently active

Current Senior Leaders Researchers

1
Jianbo Wang
Baoding People's Hospital
2
Huw M. L. Davies
Emory University
3
Frank Glorius
University of Münster
4
Min Shi
Guiyang University
5
F. Dean Toste
University of California System
6
Antonio M. Echavarren
Institut Català d'Investigació Química
7
Junliang Zhang
Fudan University
8
Vladimir Gevorgyan
The University of Texas at Dallas
9
Jin‐Quan Yu
Scripps Research Institute
10
K. N. Houk
University of California System

Current Senior Leaders Papers

1
An overview of N-heterocyclic carbenes
Nature|2014
4.2k cit.
2
Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions
Accounts of Chemical Research|2011
2.7k cit.
3
C–H bond activation enables the rapid construction and late-stage diversification of functional molecules
Nature Chemistry|2013
2.4k cit.
4
Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
Angewandte Chemie International Edition|2012
1.6k cit.
5
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O<sub>2</sub> as an Oxidant
Journal of the American Chemical Society|2006
1.4k cit.
6
Benchmarking the Conductor-like Polarizable Continuum Model (CPCM) for Aqueous Solvation Free Energies of Neutral and Ionic Organic Molecules
Journal of Chemical Theory and Computation|2004
1.3k cit.
7
The Measure of All Rings—N‐Heterocyclic Carbenes
Angewandte Chemie International Edition|2010
1.2k cit.
8
Palladium(II)‐katalysierte C‐H‐Aktivierung/C‐C‐Kreuzkupplung: Vielseitigkeit und Anwendbarkeit
Angewandte Chemie|2009
1.2k cit.
9
Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
Journal of the American Chemical Society|2007
991 cit.
10
Diazo Compounds and <i>N</i>-Tosylhydrazones: Novel Cross-Coupling Partners in Transition-Metal-Catalyzed Reactions
Accounts of Chemical Research|2012
971 cit.

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