Yanzhao Wang

General Research Institute for Nonferrous Metals (China)

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Liming Zhang

University of California, Santa Barbara

Long‐Wu Ye

Chinese Academy of Sciences

Yingdong Luo

South China University of Technology

Lianzhu Liu

University of California, Santa Barbara

Biao Lu

Sichuan Agricultural University

Liu‐Zhu Gong

Hefei National Center for Physical Sciences at Nanoscale

Guozhu Zhang

Central China Normal University

Ke‐Gong Ji

Northwest A&F University

Xiao‐Ying Xu

Second Affiliated Hospital of Dalian Medical University

Zhixun Wang

Merck & Co., Inc., Rahway, NJ, USA (United States)

Cooperative Institutions

Chinese Academy of Sciences

Tongji University

University of California, Santa Barbara

State Key Laboratory of Pollution Control and Resource Reuse

University of Science and Technology of China

Central China Normal University

University of Chinese Academy of Sciences

Shanghai Institute of Pollution Control and Ecological Security

Chengdu Organic Chemicals (China)

Grinm Advanced Materials (China)

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Engineering gold nanoclusters anchored cobalt oxyhydroxide with bifunction for discriminative monitoring azodicarbonamide

Food Chemistry (2025)

Shun Wang Guoming Sun Yanzhao Wang Shuo Tian Z. G. Xing

Nanoclusters

10.1016/j.foodchem.2025.143563

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Citations (0)

Synthesis of Chiral γ-Amino Alcohols via a RuPHOX-Ru Catalyzed Asymmetric Hydrogenation of β-Imide Ketones

Chinese Journal of Organic Chemistry (2014)

Yanzhao Wang Jianxia Wang Delong Liu Wanbin Zhang

RuPHOX-Ru 催化的手性

Imide

10.6023/cjoc201404035

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Citations (25)

An Au/Zn‐catalyzed Synthesis of N ‐Protected Indole via Annulation of N ‐Arylhydroxamic Acid and Alkyne

Organic Syntheses (2019)

Xinpeng Cheng Yanzhao Wang Liming Zhang

Annulation

10.1002/0471264229.os095.02

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Citations (1)

Homogeneous Gold-Catalyzed Oxidative Carboheterofunctionalization of Alkenes

Journal of the American Chemical Society (2010)

Guozhu Zhang Li Cui Yanzhao Wang Liming Zhang

Homogeneous carboamination, carboalkoxylation and carbolactonization of terminal alkenes are realized via oxidative gold catalysis, providing expedient access to various substituted N- or O-heterocycles. Deuterium-labeling studies established the anti nature of the alkene functionalization and the indispensible role of Au(I)/Au(III) catalysis. This study constitutes the first example of catalytically converting C(sp(3))-Au bonds into C(sp(3))--C(sp(2)) bonds in a cross-coupling manner and opens new opportunities to study gold alkene catalysis where alkylgold intermediates can be readily functionalized intermolecularly.

Alkene

Homogeneous Catalysis

Surface Modification

Oxidative addition

10.1021/ja909555d

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Citations (419)

Combining Gold(I)/Gold(III) Catalysis and CH Functionalization: A Formal Intramolecular [3+2] Annulation towards Tricyclic Indolines and Mechanistic Studies

Angewandte Chemie International Edition (2011)

Guozhu Zhang Yingdong Luo Yanzhao Wang Liming Zhang

Gold rush: A combination of oxidative gold(I)/gold(III) catalysis and CH functionalization led to the first oxidative coupling between in situ generated alkyl gold reagents and CH bonds, affording tricyclic indolines through a formal [3+2] annulation between a vinyl group and an aniline moiety [see scheme; Tf=trifluoromethanesulfonyl, Selectfluor=1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)]. Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Selectfluor

Moiety

Annulation

Tetrafluoroborate

Surface Modification

10.1002/anie.201100293

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Citations (125)

Copolymerization of Ethylene/Polar Monomer Catalyzed by Phosphinoarenesulfonate (PO) Metal Catalysts and the Catalytic Mechanism

Chinese Journal of Organic Chemistry (2016)

Biyun Su Peiyu Jia Yanzhao Wang Yaning Li He Huang

王彦昭 a 李亚宁 a 黄鹤 a 李谦定 a ( a 西安石油大学化学化工学院西安 710065) ( b 宁波激智科技股份有限公司宁波 315100) 摘要含有膦基苯磺酸(PO)配体的烷基金属配合物表现出罕见的烯烃聚合催化性质, 其不但可以催化乙烯均聚形成线性聚乙烯, 而且可以催化乙烯与众多的极性单体如 CH 2 ＝CHX、CO 等共聚产生功能化线性聚烯烃.总结了 PO 配体的结构特点和(PO)Pd(II)配合物引发的新型聚合反应, 综述了(PO)Ni(II)催化剂在催化乙烯和极性单体共聚方面的应用, 以及含有膦基二磺酸配体 OPO 的 Pd(II)、Ru(IV)催化剂的特殊催化性质. 另外, 从配体的对称性、柔性和轴向官能团位阻以及纯电子效应等方面对 PO 金属催化剂的构效关系和共聚催化反应机理进行了探讨.

10.6023/cjoc201603048

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Citations (2)

Hydroxy-telechelic poly(ethylene-co-isobutylene) as a soft segment for thermoplastic polyurethanes

Polymer Chemistry (2015)

Yanzhao Wang Marc A. Hillmyer

Facile preparation of linear amorphous hydroxy-telechelic poly(ethylene-co-isobutylene) (PEIB) was enabled by ROMP of a new monomer, (Z)-5,5-dimethylcyclooct-1-ene (Me₂COE).

Isobutylene

Thermoplastic elastomer

Telechelic polymer

10.1039/c5py00990a

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Citations (25)

Au-catalyzed synthesis of 2-alkylindoles from N-arylhydroxylamines and terminal alkynes

Chemical Communications (2011)

Yanzhao Wang Long‐Wu Ye Liming Zhang

The first gold-catalyzed addition of N-arylhydroxylamines to aliphatic terminal alkynes is developed to access O-alkenyl-N-arylhydroxylamines, which undergo facile in situ sequential 3,3-rearrangements and cyclodehydrations to afford 2-alkylindoles with regiospecificity and under exceptionally mild reaction conditions.

Reaction conditions

10.1039/c1cc12212f

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Citations (103)

Rapid Access to Chroman‐3‐ones through Gold‐Catalyzed Oxidation of Propargyl Aryl Ethers

Angewandte Chemie (2012)

Yanzhao Wang Ke‐Gong Ji Sylvester Lan Liming Zhang

Ruck-zuck: Chroman-3-one sind wichtige Zwischenstufen in der organischen Synthese und medizinischen Chemie, ihre Synthese erfordert aber mehrere Stufen. Eine goldkatalysierte Alkinoxidation eröffnet einen hoch effizienten Weg zu diesen vielseitigen Heterocyclen in nur zwei Stufen ausgehend von leicht zugänglichen Phenolen (siehe Schema). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Propargyl

Schema (genetic algorithms)

10.1002/ange.201107561

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Citations (61)

ChemInform Abstract: Rapid Access to Chroman-3-ones Through Gold-Catalyzed Oxidation of Propargyl Aryl Ethers.

ChemInform (2012)

Yanzhao Wang Ke‐Gong Ji Sylvester Lan Liming Zhang

Abstract An efficient one‐pot method for the synthesis of the title compounds uses easily accessible pyridine N‐oxides (I), derived from Hantzsch esters.

Propargyl

10.1002/chin.201227144

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Citations (0)