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Chemistry

D-Index
54
Citations
9272
World Ranking
12732
National Ranking
1999

Overview

Guofu Zhong is a researcher affiliated with Hangzhou Normal University in China, specializing primarily in the field of Chemistry with a strong focus on Organic Chemistry. Their work encompasses various subfields such as Inorganic Chemistry, Spectroscopy, Pharmacology, and Molecular Biology, reflecting an interdisciplinary approach.

The main topics of research include Catalytic C-H Functionalization Methods, Synthesis and Catalytic Reactions, Axial and Atropisomeric Chirality Synthesis, Catalytic Cross-Coupling Reactions, Asymmetric Hydrogenation and Catalysis, Asymmetric Synthesis and Catalysis, and Synthetic Organic Chemistry Methods.

Frequent coauthors in their publications include Jian Zhang, Xiaofei Zeng, Yuhang Zhu, Liyuan Ding, and Wenzhou Shen, indicating active collaboration within their research network.

Zhong's research outputs have appeared multiple times in notable scientific journals. The most common publication venues for their work are:

  • Organic Chemistry Frontiers
  • Organic Letters
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • The Chemical Record

Selected recent papers authored or coauthored by Guofu Zhong include:

  • Recent advances in chelation-assisted site- and stereoselective alkenyl C-H functionalization, 2021, Chemical Society Reviews
  • Design and Atroposelective Construction of IAN analogues by Organocatalytic Asymmetric Heteroannulation of Alkynes, 2020, Angewandte Chemie International Edition
  • Photocatalyst-free visible-light-mediated three-component reaction of α-diazoesters, cyclic ethers and NaSCN to access organic thiocyanates, 2022, Chinese Chemical Letters
  • Nitrosobenzene-Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N-Arylbenzimidazoles, 2021, Angewandte Chemie International Edition
  • A Dynamic Kinetic Resolution Approach to Axially Chiral Diaryl Ethers by Catalytic Atroposelective Transfer Hydrogenation, 2022, Angewandte Chemie International Edition

Best Publications

  • A Facile and Rapid Route to Highly Enantiopure 1,2-Diols by Novel Catalytic Asymmetric α-Aminoxylation of Aldehydes†

    Guofu Zhong

  • A highly enantioselective amino acid-catalyzed route to functionalized α-amino acids

    Armando Cordova;Wolfgang Notz;Guofu Zhong;Juan M. Betancort

  • Recent Progress of Metal Sulfide Photocatalysts for Solar Energy Conversion

    Unknown

  • Immune versus natural selection: antibody aldolases with enzymic rates but broader scope.

    Carlos F. Barbas;Andreas Heine;Guofu Zhong;Torsten Hoffmann

  • Aldolase Antibodies of Remarkable Scope

    Torsten Hoffmann;Guofu Zhong;Benjamin List;Doron Shabat

  • Amine-catalyzed direct asymmetric Mannich-type reactions

    Wolfgang Notz;Kandasamy Sakthivel;Tommy Bui;Guofu Zhong

  • Antibody-Catalyzed Enantioselective Robinson Annulation

    Guofu Zhong;Torsten Hoffmann;Richard A. Lerner;Samuel Danishefsky

  • Chiral Brønsted Acid-Catalyzed Enantioselective α-Hydroxylation of β-Dicarbonyl Compounds

    Min Lu;Di Zhu;Yunpeng Lu;Xiaofei Zeng

  • Recent advances in chelation-assisted site- and stereoselective alkenyl C-H functionalization.

    Jian Zhang;Xiunan Lu;Cong Shen;Liangyao Xu

  • Organocatalytic asymmetric tandem Michael-Henry reactions: a highly stereoselective synthesis of multifunctionalized cyclohexanes with two quaternary stereocenters.

    Bin Tan;Pei Juan Chua;Yongxin Li;Guofu Zhong

  • Broadening the Aldolase Catalytic Antibody Repertoire by Combining Reactive Immunization and Transition State Theory: New Enantio‐ and Diastereoselectivities

    Guofu Zhong;Richard A. Lerner;Carlos F. Barbas

  • The Scope of the Direct Proline-Catalyzed Asymmetric Addition of Ketones to Imines

    Wolfgang Notz;Shin‐ichi Watanabe;Naidu S. Chowdari;Guofu Zhong

  • Facile Domino Access to Chiral Bicyclo[3.2.1]octanes and Discovery of a New Catalytic Activation Mode

    Bin Tan;Yunpeng Lu;Xiaofei Zeng;Pei Juan Chua

  • Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Bronsted Acid Catalysis

    Dan Shen;Qiliang Chen;Peipei Yan;Xiaofei Zeng

  • N-heterocyclic carbene (NHC)-catalyzed highly diastereo- and enantioselective oxo-Diels-Alder reactions for synthesis of fused pyrano[2,3-b]indoles.

    Limin Yang;Fei Wang;Pei Juan Chua;Yunbo Lv

  • Organocatalytic Asymmetric α‐Aminoxylation/Aza‐Michael Reactions for the Synthesis of Functionalized Tetrahydro‐1,2‐oxazines

    Min Lu;Di Zhu;Yunpeng Lu;Yuxuan Hou

  • Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins.

    Bin Tan;Xiaofei Zeng;Yunpeng Lu;Pei Juan Chua

  • Control of four stereocenters in an organocatalytic domino double Michael reaction: efficient synthesis of multisubstituted cyclopentanes.

    Bin Tan;Zugui Shi;Pei Juan Chua;Guofu Zhong

  • Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.

    Danbo Xie;Limin Yang;Youqiang Lin;Zhiming Zhang

  • Enantioselective synthesis of allylic alcohols by the sequential aminoxylation-olefination reactions of aldehydes under ambient conditions.

    Guofu Zhong;Yongping Yu

  • Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: highly efficient and stereocontrolled syntheses of 3,3'-pyrrolidonyl spirooxindoles

    Bin Tan;Bin Tan;Xiaofei Zeng;Xiaofei Zeng;Wendy Wen Yi Leong;Wendy Wen Yi Leong;Zugui Shi;Zugui Shi

  • Organocatalytic asymmetric alpha-aminoxylation/aza-Michael reactions for the synthesis of functionalized tetrahydro-1,2-oxazines.

    Unknown

Frequent Co-Authors

Bin Tan
Bin Tan Southern University of Science and Technology
Carlos F. Barbas
Carlos F. Barbas Scripps Research Institute
Richard A. Lerner
Richard A. Lerner Scripps Research Institute
Benjamin List
Benjamin List Max Planck Society
Doron Shabat
Doron Shabat Tel Aviv University
Teck-Peng Loh
Teck-Peng Loh Nanyang Technological University
Yongxin Li
Yongxin Li Nanyang Technological University
Ian A. Wilson
Ian A. Wilson Scripps Research Institute
Fujie Tanaka
Fujie Tanaka Okinawa Institute of Science and Technology
Christoph Rader
Christoph Rader Scripps Research Institute

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