2019年
173、 Peichao Zhang, Jie Han and Junliang Zhang* Angew. Chem. Int. Ed. 2019, 58, 10.1002/anie.201904805.
170、 Huamin Wang, Junyou Zhang, Youshao Tu and Junliang Zhang* Angew. Chem. Int. Ed. 2019, 58, 5422-5426.
169、 Chenghao Zhu, Junliang Zhang* Chem. Commun., 2019, 55, 2793—2796.
168、 Bing Liu, Wenbo Li, Hai-Hong Wu *, Junliang Zhang*. Org. Chem. Front., 2019, 6, 694–698.
167、 Lei Wang, Mingjie Chen, Junliang Zhang*. Org. Chem. Front., 2019, 6, 32–35.
2018年
162、 Tao-Yan Lin, Hai-Hong Wu, Jian-Jun Feng, Junliang Zhang* Org. lett., 2018, 20 , 3587–3590.
161、 Bing Xu, Zhan-Ming Zhang, Lujia Zhou, Junliang Zhang* Org. Lett., 2018, 20, 2716-2719.
159、 Mei Zhang, Xiaoyu Di, Mingrui Zhang, Junliang Zhang* Chin. J. Chem, 2018, 36, 519-525.
158 、Shan Xu, Bing Liu, Zhan-Ming Zhang, Bing Xu, Junliang Zhang* Chin. J. Chem. 2018, 36, 421-429.
157、 Chao-Ze Zhu, Jian-Jun Feng, Junliang Zhang* Chem. Commun., 2018, 54, 2401-2404.
156、 Qin Zeng, Li Zhang, Yuanjing Xiao,* Junliang Zhang* Org. Biomol. Chem, 2018, 16, 1375-1380.
155、 Qiang Dai, Junliang Zhang* Adv. Synth. Catal., 2018, 360, 1123-1127.
154、 Peng Chen, Junyou Zhang, Junliang Zhang* Adv. Synth. Catal., 2018, 360, 682-685.
153、 Pei-Chao Zhang, Yidong Wang, Zhan-Ming Zhang, Junliang Zhang* Org. Lett, 2018, 20, 7049-7052.
152、 Tao Zhou, Tong Xia, Zhenli Liu, Lu Liu,* Junliang Zhang* Adv. Synth. Catal.,2018, 360, 4475-4479.
149、 Yidong Wang, Zhan-Ming Zhang, Feng Liu, Yinyan He, Junliang Zhang* Org. Lett. 2018, 20, 6403-6406.
148、 Ben Ma, Lu Liu,* Junliang Zhang* Asian J. Org. Chem., 2018, 7, 2015-2025.
147、 Bing Liu, Hai-Hong Wu, Junliang Zhang* ACS .Catal., 2018, 8, 8318-8323.
2017年
145、 Chao-Ze Zhu, Jian-Jun Feng,* and Junliang Zhang* Angew. Chem. Int. Ed. 2017, 56, 1351-1355.
144. Ben Ma, Zhaowei Chu, Ben Huang, Zhenli Liu, Lu Liu* and Junliang Zhang*
143. Chao-Ze Zhu, Jian-Jun Feng* and Junliang Zhang*
Rhodium(I)-Catalyzed Intermolecular Aza-[4+3] Cycloaddition of Vinyl Aziridines and Dienes: Atom-Economical Synthesis of nantiomerically Enriched Functionalized Azepines. Angew. Chem. Int. Ed., 2017, 56, 1351-1355.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201609608/full
142. , and
http://onlinelibrary.wiley.com/doi/10.1002/chem.201602822/full
141. Bing Xu,‡ Zhan-Ming Zhang,‡ Shan Xu, Bing Liu, Yuanjing Xiao and Junliang Zhang*
Copper(I)/Ming-Phos-Catalyzed Asymmetric Intermolecular [3+2] Cycloaddition of Azomethine Ylides with α-Trifluoromethyl α,β-Unsaturated Esters. ACS Catal. 2017, 7, 210−214.
‡ These authors contributed equally to this work
140、 Xiaofan Zhou,Chaoqian Huang, Yu Zeng, Jiarui Xiong, Yuanjing Xiao*, Junliang Zhang* Chem. Commun. 2017,53, 1084 – 1087.
139、Jieru Yang, Xiaofan Zhou,Yu Zeng, Chaoqian Huang, Yuanjing Xiao*, Junliang Zhang* Org. Biomol. Chem., 2017, 15, 2253–2258.
138、Huamin Wang, Wei Zhou, Mengna Tao, Anjing Hu, Junliang Zhang* Org. Lett. 2017, 19, 1710 – 1713.
137、Shenhuan Li, Yuanyuan Liu, Ben Huang, Tao Zhou, Hongmei Tao, Yuanjing Xiao, Lu Liu*, Junliang Zhang* ACS. Catal. 2017,7, 2805 – 2809.
136、Taoyan Lin,Haihong Wu, Jianjun Feng, Junliang Zhang* Org. Lett. 2017, 19, 2897 – 2900.
135、Taoyan Lin,Haihong Wu, Jianjun Feng, Junliang Zhang* ACS. Catal. 2017, 7, 4047 – 4052.
134、Peichao Zhang, Yidong Wang, Deyun Qian, Wenbo Li, Junliang Zhang* Chin. J. Chem. 2017,35, 849 – 852.
133、Xingxing Wu, Wei Zhou, Haihong Wu, Junliang Zhang* Chem. Commun. 2017, 53, 5661 – 5664.
132、Chaoze Zhu, Jianjun Feng, Junliang Zhang* Chem. Commun. 2017 , 53, 4688 – 4691.
131、Wei Zhou, HuaminWang, Mengna Tao, Chaoze Zhu, Taoyan Lin, Junliang Zhang* Chem. Sci. 2017, 8, 4660 – 4665.
130、Bing Xu, Zhanmin Zhang, Bing Liu, Shan Xu, Liejin Zhou, Junliang Zhang* Chem. Commun. 2017, 53, 8152 – 8155.
129、 Lu Liu, Junliang Zhang* Chin. J. Org. Chem. 2017,37,1117 – 1126.
128、Jianjun Feng, Junliang Zhang* ACS. Catal. 2017, 7, 1533 – 1542.
127、Yuanyuan Liu, Wenbo Li, Junliang Zhang* Natl. Sci. Rev. 2017, 4, 326 – 358.
126、Bing Liu, Zhanmin Zhang, Bing Xu, Shan Xu, Haihong Wu, Yuanyuan Liu, Junliang Zhang* Org. Chem. Front. 2017, 4, 1772 – 1776.
125、Yu Zeng, Chaoqian Huang, PeiyunNi, Lu Liu, Yuanjing Xiao*, Junliang Zhang* Adv. Synth. Catal. 2017, 359, 3555 – 3559.
124、Ben Ma, Jiaojiao Wu, Lu Liu*, Junliang Zhang* Chem. Commun. 2017 ,53, 10164 – 10167.
123、Chaoqian Huang, Yu Zeng, Huayu Cheng, Anjing Hu, Lu Liu, Yuanjing Xiao*, JunliangZhang* Org. Lett. 2017,19, 4968 – 4971.
122、MengnaTao, Wei Zhou, Junliang Zhang* Adv. Synth. Catal. 2017, 359, 3347 – 3353.
121、Huamin Wang, Weike Lu, Junliang Zhang* Chem. Eur. J. 2017, 23, 13587 – 13590.
120、Tao Zhou, Shenhuan Li, Ben Huang, Chao Li, Yang Zhao, Jieqiong Chen, Aoling Chen, Yuanjing Xiao, Lu Liu*, Junliang Zhang* Org. Biomol. Chem., 2017, 15, 4941–4945.
119、Ben Huang, Chao Li, Huamin Wang, Caihui Wang, Lu Liu*, Junliang Zhang* Org. Lett. 2017, 19, 5102−5105.
118、Taoyan Lin, Haihong Wu, Jianjun Feng*, Junliang Zhang* Org. Lett. 2017, 19, 6526–6529.
117、 Junyou Zhang, Haihong Wu*, Junliang Zhang* Org. Lett. 2017, 19, 6080−6083.
116、Chaoze Zhu, Jianjun Feng,* junliang Zhang* Chin. J. Org. Chem. 2017, 37, 1165-1172.
115. W. Zhou, L. Gao, M. Tao, X. Su, Q. Zhao, J. Zhang, Acta Chim. Sinica 2016, 74, 800-804.
114. W. Zhou, Z. Yue, J. Zhang, Org. Chem. Front. 2016, 3, 1416.
113.Zhunzhun Yu,Yongfeng Li, Jiameng Shi, Ben Ma, Lu Liu and Junliang Zhang*
(C6F5)3B -Catalyzed Highly Chemoselective and Ortho-selective C-H Bond Functionalization of Phenols Oriented by Hydrogen Bonds. Angew.Chem. Int. Ed., 2016, 55, 14807-14811.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201608937/full
112. Feng, Jian-Jun;* Zhang, Junliang*
Synthesis of Unsaturated N-Heterocycles by Cycloadditions of Aziridines and Alkynes. ACS Catal. 2016, 6, 6651-6661. (Invited Review)
http://pubs.acs.org/doi/abs/10.1021/acscatal.6b02072
111. Peng Chen, Zhenting Yue, Junyou Zhang, Xi Lv, Lei Wang and Junliang Zhang*
Phosphine-Catalyzed Asymmetric Umpolung Addition of Trifluoromethyl Ketimines to Morita–Baylis–Hillman Carbonates. Angew. Chem. Int. Ed.2016, 55, 13316-13320.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201607918/full
110. Zhenting Yue, Wenbo Li, Lu Liu, Cuihong Wang* and Junliang Zhang*
Enantioselective Synthesis of 4H-Pyrans Through Organocatalytic Asymmetric Formal [3+3] Cycloadditions of 2-(1-Alkynyl)-2-alken-1-ones with β-Keto Esters. Adv. Synth. Catal. 2016, 3015-3020 (VIP).
http://onlinelibrary.wiley.com/doi/10.1002/adsc.201600591/full
109. Lin, Tao-Yan; Zhu, Chao-Ze; Zhang, Peichao; Wang, Yidong; Wu, Hai-Hong; Feng, Jian-Jun;* Zhang, Junliang*
Regiodivergent Intermolecular [3+2] Cycloadditions of Vinyl Aziridines and Allenes: Stereospecific Synthesis of Chiral Pyrrolidines”, Angew. Chem. Int. Ed. 2016, 55, 10844-10848.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201605530/full
108. WenboLi, Xiuzhao Yu, Zhenting Yue, and Junliang Zhang*
Asymmetric Construction of 2,3-Dihydroisoxazoles via an Organocatalytic Formal [3 + 2] Cycloaddition of Enynes withN-Hydroxylamines. Org. Lett. 2016, 18, 3972–3975
http://pubs.acs.org/doi/abs/10.1021/acs.orglett.6b01737
107. Ben Ma, Ziang Wu, Ben Huang, Lu Liu* and Junliang Zhang*
Gold-catalysed facile access to indene scaffold via sequential C-H functionalization and 5-endo-dig carbocyclization. Chem. Commun, 2016, 52, 9351-9354.
http://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc04034a
106. Wei Zhou, Peng Chen, Mengna Tao, Xiao Su, Qingjie Zhao* and Junliang Zhang*
Enantioselective intermolecular cross Rauhut–Currier reactions of activated alkenes with acrolein. Chem. Commun, 2016, 52, 7612-7615.
http://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc02742c#!divAbstract
105.ZhunZhun Yu, Lu Liu* and Junliang Zhang*
Triflic Acid-Catalyzed Enynes Cyclization: A New Strategy beyond Electrophilic π-Activation. Chem. Eur. J., 2016, 22, 8488-8492
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201601599/abstract
104. Haoxiang Hu, Yidong Wang, Deyun Qian, Zhan-Ming Zhang, Lu Liu* and Junliang Zhang*
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone. Org. Chem. Front., 2016, 3, 759-763.
http://pubs.rsc.org/en/content/articlelanding/2016/qo/c6qo00087h/unauth#!divAbstract
103.Zhan-Ming Zhang,‡ Bing Xu,‡ Shan Xu, Hai-Hong Wu and Junliang Zhang*
Diastereo- and Enantioselective Copper(I)-Catalyzed Intermolecular [3+2] Cycloaddition of Azomethine Ylides with β-Trifluoromethyl β,β-Disubstituted Enones. Angew. Chem. Int. Ed. 2016, 55, 6324–6328.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201602542/full
‡ These authors contributed equally to this work
102. Jieru Yang, Xiaofan Zhou, Yu Zeng, Chaoqian Huang, Yuanjing Xiao* and Junliang Zhang*
Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates. Chem. Commun., 2016, 52, 4922.
http://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc00831c
101.Jian-Jun Feng,‡ Tao-Yan Lin,‡ Chao-Ze Zhu, Huamin Wang, Hai-Hong Wu and Junliang Zhang*
The Divergent Synthesis of Nitrogen Heterocycles by Rhodium(I)-Catalyzed Intermolecular Cycloadditions of Vinyl Aziridines and Alkynes. J. Am. Chem. Soc. 2016, 138, 2178-2181.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b00386
‡ These authors contributed equally to this work
100.Wenbo Li and Junliang Zhang*
Recent developments in the synthesis and utilization of chiral β-aminophosphine derivatives as catalysts or ligands. Chem. Soc. Rev.2016, 45, 1657-1677.
http://pubs.rsc.org/en/content/articlelanding/2016/cs/c5cs00469a#!divAbstract
99. Peng Chen, Xiao Su, Wei Zhou, Yuanjing Xiao* and Junliang Zhang*
Novel Chiral Sulfinamide Phosphines : Valuable Precursors to Chiral β-Aminophosphines. Tetrahedron 2016, 72, 2700-2706.
http://www.sciencedirect.com/science/article/pii/S0040402015302532
98.Yanqing Zhang, Yuanjing Xiao* and Junliang Zhang*
Gold(I)-Catalyzed Stereospecific [4+3]-Cycloaddition Reaction of 1-(Alk-1-ynyl)cyclopropyl Ketones with Nitrones: A Modular Entry to Enantioenriched 5,7-Fused Bicyclic Furo[3,4-d][1,2]oxazepines. Synthesis 2016, 48, 512-519. (Invited feature article)
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1561276
97. Lu Liu* and Junliang Zhang*
Gold-catalyzed transformations of α-diazocarbonyl compounds: selectivity and diversity. Chem. Soc. Rev. 2016, 45, 506-516.
http://pubs.rsc.org/en/content/articlelanding/2015/cs/c5cs00821b#!divAbstract
96. Zhunzhun Yu, Haile Qiu, Lu Liu* and Junliang Zhang*
Gold-Catalyzed Construction of Two Adjacent Quaternary Stereocenters via Sequential C-H Functionalization and Aldol Annulation. Chem. Commun. 2016, 52, 2257-2260.
http://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc08880a#!divAbstract
95 Wenbo Li, Liejing Zhou and Junliang Zhang*
Recent Progress in Dehydro(genative) Diels–Alder Reaction. Chem. Eur. J. 2016, 22, 1558-1571. (Invited Reviews)
http://onlinelibrary.wiley.com/doi/10.1002/chem.201503571/full
94 Yuan Liu,‡ Zhunzhun Yu,‡ John Zenghui Zhang, Lu Liu,* Fei Xia* and Junliang Zhang*
Origins of Unique Gold-Catalyzed Chemo- and Site-Selective C-H Functionalization of Phenols with Diazo Compounds. Chem. Sci.2016,7, 1988-1995.
http://pubs.rsc.org/en/content/articlelanding/2015/sc/c5sc04319k#!divAbstract
‡ These authors contributed equally to this work
93 Jian-Jun Feng, Tao-Yan Lin, Hai-Hong Wu, and Junliang Zhang*
Modular Access to the Stereoisomers of Fused Bicyclic Azepines: Rhodium-Catalyzed Intramolecular Stereospecific Hetero-[5+2] Cycloaddition of Vinyl Aziridines and Alkenes. Angew. Chem. Int. Ed. 2015, 54, 15854-15858.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201509185/abstract
92 Mingjin Chen, Zhan-Ming Zhang, Zhunzhun Yu, Haile Qiu, Ben Ma, Hai-Hong Wu* and Junliang Zhang*
Polymer-Bound Chiral Gold-Based Complexes as Efficient Heterogeneous Catalysts for Enantioselectivity Tunable Cycloaddition. ACS Catal. 2015, 5, 7488−7492.
http://pubs.acs.org/doi/abs/10.1021/acscatal.5b01963
91 Wenbo Li, Lihua Gao, Zhenting Yue and Junliang Zhang*
Phosphine-Catalyzed Regioselective and Stereoselective Hydrohalogenation Reaction of 2-(1-Alkynyl)-2-alken-1-ones: Synthesis of 2-Halo-1,3-dienes.Adv. Synth. Catal. 2015, 357, 2651-2655.
http://onlinelibrary.wiley.com/doi/10.1002/adsc.201500408/abstract
90 Wei Zhou, Xiao Su, Mengna Tao,Chaoze Zhu, Qingjie Zhao* and Junliang Zhang*
A Novel Chiral Sulfinamide Bisphosphine Catalysts: Design, Synthesis, and Application in Highly Enantioselective Inter-molecular Cross Rauhut–Currier Reactions. Angew. Chem. Int. Ed. 2015, 54, 14853-14857
http://onlinelibrary.wiley.com/doi/10.1002/anie.201508108/abstract
89 Yidong Wang, Peichao Zhang, Deyun Qian and Junliang Zhang*
Highly Regio-, Diastereo-, and Enantioselective Gold(I)-Catalyzed Intermolecular Annulations with N-Allenamides at the Proximal C=C Bond. Angew. Chem. Int. Ed. 2015, 54, 14849-14852 (Cover paper).
（Highlighted by Synfacts 2015, 11, 1302）
http://onlinelibrary.wiley.com/doi/10.1002/anie.201507165/abstract
88 Yidong Wang, Peichao Zhang, Yuan Liu, Fei Xia* and Junliang Zhang*
Enantioselective Gold-Catalyzed Intermolecular [2+2] versus [4+2]-Cycloadditions of 3-Styrylindoles with N-Allenamides: Oberservation of Interesting Substituent Effect. Chem. Sci. 2015, 6, 5564-5570.http://pubs.rsc.org/en/content/articlelanding/2015/sc/c5sc01827g#!divAbstract
（Highlighted by Synfacts 2016, 12, 55）
87 Yangyan Li, Xiao Su, Wei Zhou, Wenbo Li and Junliang Zhang*
Amino Acid Derived Phosphine-Catalyzed Enantioselective 1,4-Dipolar Spiroannulation of Cyclobutenones and Isatylidenemalononitrile. Chem. Eur. J.2015, 21, 4224-4228.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201406475/abstract
86 Liejin Zhou, Bing Xu and Junliang Zhang*
Metal-free Dehydrogenative Diels-Alder Reactions of 2-Methyl, 3-Aryl-methyl-indoles and Dienophiles：A Rapid Access to Tetrahydrocarbazoles, Carbazoles and Heteroacenes. Angew. Chem. Int. Ed.2015, 54, 9092-9096.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201503549/abstract
85 Feng Liu, Yidong Wang, Weiming Ye, and Junliang Zhang*
Gold(I)-catalyzed asymmetric [3 + 2]-cycloadditions of γ-1-ethoxyethoxy-propiolates and aldehydes. Org. Chem. Front.2015, 2, 221-225.
http://pubs.rsc.org/en/content/articlelanding/2015/qo/c4qo00261j#!divAbstract
84 Xiao Su, Wei Zhou, Yangyan Li, and Junliang Zhang*
Design, Synthesis, and Application of a Chiral Sulfinamide Phosphine Catalyst for the Enantioselective Intramolecular Rauhut–Currier Reaction. Angew. Chem. Int. Ed.2015, 54, 6874-6877.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201500907/abstract
83 Jieru Yang, Ao Mao, Zhenting Yue, Wenxuan Zhu, Xuewei Luo, Chuwei Zhu, Yuanjing Xiao* and Junliang Zhang*
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C–F substitutions. Chem. Commun.2015, 51, 8326-8329.
http://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc02073e#!divAbstract
(Highlighted by http://x-mol.com/news/508)
82 Jian-Jun Feng, Tao-Yan Lin, Hai-Hong Wu and Junliang Zhang*
Transfer of Chirality in the Rhodium-Catalyzed Intramolecular Formal Hetero-[5 + 2] Cycloaddition of Vinyl Aziridines and Alkynes: Stereoselective Synthesis of Fused Azepine Derivatives. J. Am.Chem. Soc. 2015, 137, 3787-3790.
http://pubs.acs.org/doi/abs/10.1021/jacs.5b01305
81. Deyun Qian and Junliang Zhang*
Gold-Catalyzed Cyclopropanation Reactions by Carbenoid Precursor Toolbox. Chem. Soc. Rev. 2015, 44, 677-698. (Cover paper)
http://pubs.rsc.org/en/content/articlelanding/2015/cs/c4cs00304g#!divAbstract
80. Li Zhang,Qin Zeng, Ao Mao, Ziang Wu, Tian Luo, Yuanjing Xiao* and Junliang Zhang*
NIS-mediated oxidative cyclization of N-(2-trifluoromethyl-3-alkynyl) hydroxylamines: a facile access to 4-trifluoromethyl-5-acylisoxazoles. Org. Biomol. Chem.2014,12, 8942-8946.
http://pubs.rsc.org/en/content/articlelanding/2014/ob/c4ob01790k
79. Deyun Qian, Haoxiang Hu, Feng Liu, Bin Tang, Weimin Ye, Yidong Wang and Junliang Zhang*
Gold(I)-Catalyzed Highly Diastereo- and Enatioselective Alkyne Oxidation/Cyclopropanation of 1,6-Enynes. Angew. Chem. Int. Ed.2014, 53, 13751-13755.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201407717/abstract
78. Lu Liu and Junliang Zhang*
Product Selectivity Control in the Domino Cyclization of 2-(2-Alkynylarylidene)-1,3-dicarbonyl Compounds Catalyzed by Metal Lewis Acids. Synthesis, 2014, 46, 2133-2142. (Invited feature article)
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0034-1378392
77. Lai Wei, Lu Liu* and Junliang Zhang*
Scandium-Catalyzed Tandem Selective Oxirane Ring-opening / Friedel-Crafts Alkylation: A Facile Access to [1,4]Oxazino[4,3-a]indoles and 3,4-Dihydro-1H-pyrrolo[2,1-c][1,4]oxazines. Org. Biomol. Chem.2014,12, 6869-6877.
http://pubs.rsc.org/en/content/articlelanding/2014/ob/c4ob01057d
76. Weimin Ye, Wenbo Li and Junliang Zhang*
A metal-free dyotropic-like rearrangement of 2-oxa allylic alcohols in the presence of organoboronic acids. Chem. Commun., 2014,50, 9879-9882
http://pubs.rsc.org/en/content/articlelanding/2014/cc/c4cc03450c
75. Liejin Zhou, Mingrui Zhang, Wenbo Li and Junliang Zhang*
Furan-Based o-Quinodimethanes by Gold-Catalyzed Dehydrogenative Heterocyclization of 2-(1-Alkynyl)-2-alken-1-ones: A Modular Entry to 2,3-Furan Fused Carbocycles. Angew. Chem. Int. Ed. 2014, 53, 6542-6545.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201403709/abstract
74. Zhunzhun Yu, Ben Ma, Mingjin Chen, Hai-Hong Wu, Lu Liu* and Junliang Zhang*
Highly Site-selective Direct C-H Bond Functionalization of Phenols with α-Aryl-α-Diazoacetates and Diazooxindoles via Gold Catalysis. J. Am. Chem. Soc. 2014, 136, 6904-6907. (Featured in JACS Spotlights：J. Am. Chem. Soc. 2014, 136, 7187−7188 http://pubs.acs.org/doi/pdf/10.1021/ja504672f，当月JACS Most Read Articles top 3，同时被SCIENCE CHINA Chemistry 2014, 57, 1057重点评述)
http://pubs.acs.org/doi/abs/10.1021/ja503163k
73. Deyun Qian and Junliang Zhang*
Gold-Catalyzed Cascade Reactions for Synthesis of Carbo- and Heterocycles: Selectivity and Diversity. Chem. Rec. 2014, 14, 280-302. (Invited Account)
http://onlinelibrary.wiley.com/doi/10.1002/tcr.201300039/abstract
72. Zhan-Ming Zhang, Peng Chen, Wenbo Li, Yanfei Niu, Xiao-Li Zhao and Junliang Zhang*
A New Type of Chiral Sulfinamide Monophosphine Ligands: Stereodivergent Synthesis and Application in Enantioselective Gold(I)-Catalyzed Cycloaddition Reactions. Angew. Chem. Int. Ed. 2014, 53, 4350-4354.
http://onlinelibrary.wiley.com/doi/10.1002/anie.201401067/abstract
71. Ziqi Tian, Yuanjing Xiao, Xiangai Yuan, Zuliang Chen, Junliang Zhang*, and Jing Ma*
Control of Chemoselectivity by Coordinated Water and Relative Size of Ligands to Metal Cations of Lewis Acid Catalysts for Cycloaddition of an Oxirane Derivative to an Aldehyde: Theoretical and Experimental Study. Organometallics2014, 33, 1715-1725.
70. Qin Zeng, Li Zhang, Jieru Yang, Bing Xu, Yuanjing Xiao*and Junliang Zhang*
Pyrroles versus cyclic nitrones: catalyst-controlled divergent cyclization of N-(2-perfluoroalkyl-3-alkynyl) hydroxylamines. Chem. Commun.2014, 50, 4203-4206.
69. Wenbo Li and Junliang Zhang*
Phosphine-Mediated Regio- and Stereoselective Hydrocarboxylation of Enynes. Org. Lett.2014, 16, 162-165.
68. Mingrui Zhang and Junliang Zhang*
Base-Catalyzed Tandem Michael/Dehydro-Diels-Alder Reaction of α,α-Dicyanoolefins with Electron-Deficient 1,3-Conjugated Enynes: A Facile Entry to Angularly Fused Polycycles. Chem. Eur. J.2014, 20, 399-404.
67. Hui Qian, Xiuzhao Yu, Junliang Zhang* and Jianwei Sun*
Organocatalytic Enantioselective Synthesis of 2,3-Allenoates by Intermolecular Addition of Nitroalkanes to Activated Enynes. J. Am. Chem. Soc. 2013, 135, 18020–18023.
http://pubs.acs.org/doi/abs/10.1021/ja409080v
66. Mei Zhangand Junliang Zhang*
Gold(I)-Catalyzed Diastereoselective Domino Reactions of 2-(1-Alkynyl)alk-2-en-1-one Oxime Ethers with α,β-Unsaturated Imines Consisting of 1,2-Alkyl Migration. Isr. J. Chem. 2013, 53, 911–914.
65. Junqing Zhang, Yuanjing Xiaoand Junliang Zhang*
Nickel-Catalyzed Annulation of Donor–Acceptor Oxiranes with Imines: Diastereoselective Access to Highly Substituted 2,4-trans-Oxazolidines. Adv. Synth. Catal. 2013, 355, 2793-2797.
64. Jieming Zhang, Hai-Hong Wu and Junliang Zhang*
Cesium Carbonate Mediated Borylation of Aryl Iodides with Diboron in Methanol. Eur. J. Org. Chem.2013, 6263-6266.
63. Zuliang Chen, Yuanjing Xiao and Junliang Zhang*
Reaction of Two Differently Functionalized Oxiranes with Nickel Perchlorate: A Modular Entry to Highly Substituted 1,3-Dioxolanes. Eur. J. Org. Chem.2013, 4748-4751.
62. Renrong Liu and Junliang Zhang*
Organocatalytic Michael Addition of Indoles to Isatylidene-3-acetaldehydes: Application to the Formal Total Synthesis of (-)-Chimonanthine. Org. Lett. 2013, 15, 2266-2269..
61. Renrong Liu and Junliang Zhang*
Organocatalytic Michael Addition of Malonates to Isatylidene-3-acetaldehydes: Application to the Total Synthesis of (-)-Debromoflustramine E. Chem. Eur. J. 2013, 19, 7319-7323.
60. Deyun Qian and Junliang Zhang*
Gold/Bronsted Acid Relay Catalysis for Enantioselective Construction of Spirocyclic Diketones. Chem. Eur. J. 2013, 19, 6984-6988.
59. Xingxing Wu, Lei Liand Junliang Zhang*
Direct aza-Darzens Aziridination of N-Tosyl Imines with 2-Bromomalonates for Efficient Synthesis of Highly Functionalized Donor-acceptor Aziridines. Adv. Synth. Catal. 2012, 354, 3485-3489.
http://onlinelibrary.wiley.com/doi/10.1002/adsc.201200628/abstract
58. Xingxing Wu and Junliang Zhang*
Y(OTf)3-Catalyzed Diastereoselective [3+2]Cycloaddition of N-Tosylaziridines and Imines; Efficient Synthesis of Multisubstituted Imidazolidines.Synthesis2012, 44, 2147-2154.
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0031-1290816
57. Yanqing Zhang and Junliang Zhang*
Highly Substituted Pyrroles by Gold(I)-Catalyzed Tandem Reaction of 1-(1-Alkynyl)cyclopropyl Oxime Ethers with Nucleophiles.Synlett,2012, 23, 1389-1393.
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0031-1290978
56. Renrong Liu and Junliang Zhang*
Palladium(II)-Catalyzed Stereospecific Three-Component Domino Reactions of Diyne-enones, Nucleophiles, and Vinyl Ketones. Chem. Asian. J.2012. 7, 294-297.
http://onlinelibrary.wiley.com/doi/10.1002/asia.201100770/abstract
55. Wenbo Li, Yuying Li, Guanghua Zhou, Xiangshu Wu, and Junliang Zhang*
Gold(I)-Catalyzed Regiodivergent Rearrangements: 1,2- and 1,2’-Alkyl Migration in Skipped Alkynyl Ketones. Chem. Eur. J. 2012, 18, 15113-15121.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201201727/abstract
54. Xiuzhao Yu, and Junliang Zhang*
A Base-Promoted Tandem Cycloaddition/Air Oxidation Reaction of Electron-Deficient Conjugated Enynes and Hydrazines: Synthesis of Highly Substituted Pyrazoles. Chem. Eur. J. 2012, 18, 12945-12949.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201202583/abstract
53. Yanqing Zhang, Junliang Zhang*
Gold(I)-Catalyzed Regio- and Stereoselective 1,3-Dipolar Cycloaddition Reactions of 1-(1-Alkynyl)cyclopropyl Oximes with Nitrones: A Modular Entry to Highly Substituted Pyrrolo[3,4-d][1,2]oxazepines. Adv. Synth. Catal.2012‚ 354‚ 2556-2560.
52. Zuliang Chen, Ziqi Tian, Jieming Zhang, Jing Ma*, Junliang Zhang*
C-O Versus C-C Bond Cleavage: Selectivity Control in Lewis Acid Catalyzed Chemodivergent Cycloadditions of Aryl Oxiranyldicarboxylates with Aldehydes, and Theoretical Rationalizations of Reaction Pathways. Chem. Eur. J. 2012,18, 8591-8595.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201201453/pdf
51. Hongyin Gao, Junliang Zhang*
Cationic Rhodium(I)-Catalyzed Regioselective Tandem Heterocyclization/[3+2] Cycloaddition of 2-(1-Alkynyl)-2-alken-1-ones with Alkynes. Chem. Eur. J.2012,18, 2777-2782.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201103924/pdf
50. Deyun Qian, Junliang Zhang*
Catalytic oxidation/C–H functionalization of N-arylpropiolamides by means of gold carbenoids: concise route to 3-acyloxindoles. Chem. Commun. 2012,48, 7082-7084.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc31972a
49. Mei Zhang, Junliang Zhang*
Gold(I)-catalyzed cyclization of 2-(1-alkynyl)-alk-2-en-1-one oximes: a facile access to highly substituted N-alkoxypyrroles. Chem. Commun. 2012,48, 6399-6401.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc32510a
48. Xiuzhao Yu, Guanghua Zhou, Junliang Zhang*
DBU-catalyzed tandem additions of electron-deficient 1,3-conjugated enynes with 2-aminomalonates: a facile access to highly substituted 2-pyrrolines. Chem. Commun. 2012,48, 4002-4004.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc30840a
47. Yanqing Zhang, Junliang Zhang*
Kinetic resolution of 1-(1-alkynyl)cyclopropyl ketones by gold(I)-catalyzed asymmetric [4+3]cycloaddition with nitrones: scope, mechanism and applications. Chem. Commun. 2012,48, 4710-4712.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc30309d?page=search
46. Lai Wei, Junliang Zhang*
Efficient synthesis of isochromanones and isoquinolines viaYb(OTf)3-catalyzed tandem oxirane/aziridine ring opening/Friedel–Crafts cyclization. Chem. Commun. 2012,48, 2636-2638.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc17836b
45. Jieming Zhang, Junliang Zhang*
Ni(ClO4)2-catalysed regio- and diastereoselective [3+2] cycloaddition of indoles and aryl oxiranyl-dicarboxylates/diketones: a facile access to furo[3,4-b]indoles. Chem. Commun. 2012,48, 1817-1819.
http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc16918e
44. Jian-Jun Feng‚ Junliang Zhang*An Atom-Economic Synthesis of Bicyclo[3.1.0]hexanes by Rhodium N-Heterocyclic Carbene-Catalyzed Diastereoselective Tandem Hetero-[5 + 2] Cycloaddition/Claisen Rearrangement Reaction of Vinylic Oxiranes with Alkynes. J. Am. Chem. Soc.2011‚133‚ 7304–7307.http://pubs.acs.org/doi/pdfplus/10.1021/ja2014604
43. Deyun Qian, Junliang Zhang*
A gold(I)-catalyzed intramolecular oxidation–cyclopropanation sequence of 1,6-enynes: a convenient access to [n.1.0]bicycloalkanes. Chem. Commun. 2011,47, 11152-11154.
http://pubs.rsc.org/en/content/articlepdf/2011/cc/c1cc14788a
42. Xingxing Wu, Lei Li, Junliang Zhang*
Nickel(II)-catalyzed diastereoselective [3+2] cycloaddition of N-tosyl-aziridines and aldehydes via selective carbon–carbon bond cleavage. Chem. Commun. 2011,47, 7824-7826.
http://pubs.rsc.org/en/content/articlepdf/2011/cc/c1cc12189h
41. Lei Li,Xingxing Wu, Junliang Zhang*
Lewis acid-catalyzed formal [3+2] cycloadditions of N-tosyl aziridines with electron-rich alkenes via selective carbon–carbon bond cleavage. Chem. Commun. 2011,47, 5049-5051.
http://pubs.rsc.org/en/content/articlepdf/2011/cc/c1cc10926j
40. Lei Li‚ Junliang Zhang*Lewis Acid-catalyzed [3 + 2]Cyclo-addition of Alkynes with N-Tosyl-aziridines via Carbon–Carbon Bond Cleavage: Synthesis of Highly Substituted 3-Pyrrolines. Org. Lett.2011‚ 13‚ 5940-5943.http://pubs.acs.org/doi/pdfplus/10.1021/ol202603e
39. Zuliang Chen‚ Lai Wei‚ Zhang Junliang*
Lewis Acid Catalyzed Carbon-Carbon Bond Cleavage of Aryl Oxiranyl Diketones: Synthesis of cis-2‚5-Disubstituted 1‚3-Dioxolanes.Org. Lett.2011‚ 13‚ 1170-1173.
http://pubs.acs.org/doi/pdfplus/10.1021/ol2000292 
38. Renrong Liu, Mei Zhang‚ Junliang Zhang*
Highly regioselective Lewis acid-catalyzed [3+2] cycloaddition of alkynes with donor–acceptor oxiranes by selective carbon–carbon bond cleavage of epoxides.Chem. Commun. 2011,47, 12870-12872.
http://pubs.rsc.org/en/content/articlepdf/2011/cc/c1cc15669a
37. Xiuzhao Yu‚ Junliang Zhang* Regioselective Addition of Organometallic Reagents to 2-(1-Alkynyl)-2-alken-1-ones for an Efficient Synthesis of Substituted 1‚2-Allenyl Ketones. Adv. Synth. Catal.2011‚ 353‚ 1265-1268.http://onlinelibrary.wiley.com/doi/10.1002/adsc.201100009/pdf
36. Deyun Qian‚ Junliang Zhang*
Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions. Beilstein J. Org. Chem. 2011‚ 7‚ 808–812.(Invited contribution in honor of F. Dean Toste )
http://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-7-92.pdf
![Graphical abstract:A gold(i)-catalyzed intramolecular oxidation–cyclopropanation sequence of 1,6-enynes:a convenient access to [n.1.0]bicycloalkanes](https://faculty.ecnu.edu.cn/picture/article/1811/e3/9f/a1b8fd8f41e8b5aa874a58797541/664ff6b5-eb86-4ca5-a33d-52842c6a5a77.gif.x "Graphical abstract")
35. Hongyin Gao‚ Xingxing Wu‚ Junliang Zhang*
Gold(I)-Catalyzed‚ Highly Diastereoselective‚ Tandem Heterocyclizations/[3+2] Cycloadditions: Synthesis of Highly Substituted Cyclopenta[c]furans.Chem. Eur. J.2011‚ 17‚ 2838-28414.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201003363/pdf
34. Guanghua Zhou‚ Feng Liu‚ Junliang Zhang*
Enantioselective Gold-Catalyzed Functionalization of Unreactive sp3 C-H Bonds through a Redox–Neutral Domino Reaction.Chem. Eur. J.2011‚ 17‚3101-3104.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201100019/pdf 
33. Tao Wang‚ Junliang Zhang*
Chemoselective C-C Bond Cleavage of Epoxide Motifs: Gold(I)-Catalyzed Diastereoselective [4+3] Cycloadditions of 1-(1-Alkynyl)oxiranyl Ketones and Nitrones. Chem. Eur. J.2011‚ 17‚ 86-90.
http://onlinelibrary.wiley.com/doi/10.1002/chem.201002395/pdf
32. Tao Wang‚ Cui-Hong Wang ‚ Junliang Zhang*
Unexpected C–C bond cleavage of epoxide motif: Rhodium(I)-catalyzed tandem heterocyclization/[4+1] cycloaddition of 1-(1-alkynyl)oxiranyl ketones. Chem. Commun. 2011‚ 47‚ 5578-5580.
http://pubs.rsc.org/en/content/articlepdf/2011/cc/c0cc05650b
![Graphical abstract:Unexpected C–C bond cleavage of epoxide motif:Rhodium(i)-catalyzed tandem heterocyclization/[4+1] cycloaddition of 1-(1-alkynyl)oxiranyl ketones](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C0CC05650B "Graphical abstract")
31. Wanxiang Zhao‚ Junliang Zhang*
Rhodium-Catalyzed Tandem Heterocyclization and Carbonylative [(3+2)+1] Cyclization of Diyne-enones. Org. Lett.2011‚ 13‚ 688–691.
http://pubs.acs.org/doi/pdfplus/10.1021/ol102920f
30. Renrong Liu‚ Junliang Zhang*
Polyheterocycles by Palladium(II)-Catalyzed Oxidative Domino Reactions Involving Direct C-H Functionalization. Adv. Synth. Catal.2011‚ 353‚ 36-40.
http://onlinelibrary.wiley.com/doi/10.1002/adsc.201000670/pdf
2010年 29. Liu Lu‚ Wei Lai‚ Zhang Junliang*A Facile Route to Polysubstituted Naphthalenes and Benzofluorenols via Scandium Triflate- and Triflic Acid-Catalyzed Benzannulation of 2-(2-Alkynylarylidene)-1‚3-Dicarbonyl Compounds. Adv.Synth. Catal.2010‚ 352‚ 1920-1924.http://onlinelibrary.wiley.com/doi/10.1002/adsc.201000286/pdf28. Xiuzhao Yu‚ Bo Du‚ Kai Wang and Junliang Zhang*Highly Substituted 2‚3-Dihydroisoxazoles by Et3N-Catalyzed Tandem Reaction of Electron-Deficient 1‚3-Conjugated Enynes with Hydroxylamines. Org. Lett.2010‚ 12‚ 1876–1879.
http://pubs.acs.org/doi/pdfplus/10.1021/ol100490y
27. Xiuzhao Yu‚ Zhongyan Cao‚ Junliang Zhang*Organocatalytic hetero [4+2] cycloaddition reactions of 2-(1-alkynyl)-2-alkene-1-ones: metal-free access to highly substituted 4H-pyrans. Org. Biomol. Chem.2010‚ 8‚ 5059-5061http://pubs.rsc.org/en/content/articlelanding/2010/ob/c0ob00334d ![Graphical abstract:Organocatalytic hetero [4+2] cycloaddition reactions of 2-(1-alkynyl)-2-alkene-1-ones:metal-free access to highly substituted 4H-pyrans](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C0OB00334D "Graphical abstract")
![Graphical abstract:Rhodium-catalyzed domino heterocyclization and [(3+2)+2] carbocyclization:construction of fused tricycloheptadienes](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C0CC02382E "Graphical abstract")
![Graphical abstract:Exo/endo selectivity-control in Lewis-acid catalyzed tandem heterocyclization/formal [4+3] cycloaddition:synthesis of polyheterocycles from 2-(1-alkynyl)-2-alken-1-ones and 1,3-diphenylisobenzofuran](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C0CC02778B "Graphical abstract")
22. Guanghua Zhou‚ Junliang Zhang*
Product-selectivity control by the nature of the catalyst: Lewis acid-catalyzed selective formation of ring-fused tetrahydroquinolines and tetrahydroazepines via intramolecular redox reaction. Chem. Commun.2010‚ 46‚ 6593–6595.http://pubs.rsc.org/en/content/articlepdf/2010/cc/c0cc01946a 
http://onlinelibrary.wiley.com/doi/10.1002/anie.201003136/pdf
20. Zuliang Chen‚ Junliang Zhang*
An Unexpected Phosphine-Catalyzed Regio- and Diastereoselective [4+1] Annulation Reaction of Modified Allylic Compounds with Activated Enones. Chem. Ansia J.2010‚ 1542- 1545.
http://www3.interscience.wiley.com/journal/123452698/abstract
19. Wenbo Li‚ Yuying Li‚ Junliang Zhang*
Gold-Catalyzed Domino Reactions Consisting of Regio- and Stereoselective 1‚2-Alkyl Migration. Chem. Eur. J.2010‚ 16‚ 6447-6450.
http://www3.interscience.wiley.com/cgi-bin/fulltext/123400551/PDFSTART
18. Yanqing Zhang‚ Feng Liu‚ Junliang Zhang*Catalytic Regioselective Control in the Diastereoselective 1‚3-Dipolar Cycloaddition Reactions of 1-(1-Alkynyl)cyclopropyl Ketones with Nitrones. Chem. Eur. J.2010‚ 16‚ 6146-6150.http://www3.interscience.wiley.com/cgi-bin/fulltext/123354217/PDFSTART
17. Wanxiang Zhao‚ Junliang Zhang*
Rhodium-catalyzed tandem nucleophilic addition/bicyclization of diyne-enones with alcohols: a modular entry to 2‚3-fused bicyclic furans. Chem. Commun. 2010‚ 46‚ 4384-4386.
http://www.rsc.org/ej/CC/2010/c000883d.pdf
16. Tao Wang‚ Junliang Zhang*
Synthesis of 2-acylfurans from 3-(1-alkynyl)-2-alken-1-ones via the oxidation of gold-carbene intermediates by H2O2. Dalton Trans.2010‚ 39‚ 4270-4273.
http://www.rsc.org/ej/DT/2010/c0dt00024h.pdf
15. Xiuzhao Yu‚ Bo Du‚ Kai Wang‚ Junliang Zhang*
Highly Substituted 2‚3-Dihydroisoxazoles by Et3N-Catalyzed Tandem Reaction of Electron-Deficient 1‚3-Conjugated Enynes with Hydroxylamines. Org. Lett.2010‚ 12‚ 1876-1879.
http://pubs.acs.org/doi/pdf/10.1021/ol100490y
14. Hongyin Gao‚ Xiaoli Zhao‚ Yihua Yu‚ Junliang Zhang*
Highly Substituted Furo[3‚4-c]azepines by Gold(I)-Catalyzed Diastereoselective Tandem Double Heterocyclizations and 1‚2-Alkyl Migration. Chem. Eur. J.2010‚ 16‚ 456-459.
http://www3.interscience.wiley.com/cgi-bin/fulltext/123193390/PDFSTART
13. Yuanjing Xiao‚ Junliang Zhang*
Tetrasubstituted allenes by Pd(0)-catalyzed three-component tandem Michael addition/cross-coupling reaction. Chem. Commun.2010‚ 46‚ 752-754.
http://www.rsc.org/ej/CC/2010/b919060k.pdf
2009年12. Wenbo Li‚ Yuanjing Xiao‚ Junliang Zhang*Alkynyl Group as Activating Group: Base-Catalyzed Diastereoselective Domino Reactions of Electron-Deficient Enynes. Adv. Synth. Catal.2009‚ 351‚ 3083-3088.http://www3.interscience.wiley.com/cgi-bin/fulltext/123206975/PDFSTART
11. Zuliang Chen‚ Junliang Zhang*Highly Functionalized 4-Alkylidenebicyclo[3.1.0]hex-2-enes by Tandem Michael Addition and Annulation of Electron-Deficient Enynes. Chem. Asian J. 2009‚ 4‚ 1527-1529.http://www3.interscience.wiley.com/cgi-bin/fulltext/122573742/PDFSTART
10. Renrong Liu‚ Junliang Zhang*Tetrasubstituted Furans by Pd-II-Catalyzed Three-Component Domino Reactions of 2-(1-Alkynyl)-2-alken-1-ones with Nucleophiles and Vinyl Ketones or Acrolein. Chem. Eur. J.2009‚ 15‚ 9303-9306. http://www3.interscience.wiley.com/cgi-bin/fulltext/122536702/PDFSTART
9. Lu Liu‚ Junliang Zhang*Selectivity-Control in Lewis-acid Catalyzed Regiodivergent Tandem Cationic Cyclization/Ring Expansion Terminated by Pinacol Rearrangement. Angew. Chem. Int. Ed. 2009‚ 48‚ 6093-6096.http://www3.interscience.wiley.com/cgi-bin/fulltext/122509041/PDFSTART
8. Feng Liu‚ Yihua Yu‚ and Junliang Zhang*
Highly Substituted Furo[3‚4-d][1‚2]oxazines: Gold-Catalyzed
Regiospecific and Diastereoselective 1‚3-Dipolar Cycloaddition of 2-(1-Alkynyl)-2-alken-1-ones with Nitrones. Angew. Chem. Int. Ed.2009‚ 48‚ 5505 –5508.
http://www3.interscience.wiley.com/cgi-bin/fulltext/122465773/PDFSTART
7. Yuanjing Xiao‚ Junliang Zhang*
Furans versus 4H-pyrans: catalyst-controlled regiodivergent tandem Michael addition–cyclization reaction of 2-(1-alkynyl)-2-alken-1-ones with 1‚3-dicarbonyl compounds. Chem. Commun. 2009‚ 3954-3596.
http://www.rsc.org/Publishing/Journals/CC/article.asp?doi=b905267d
6. Yanqing Zhang‚ Zuliang Chen‚ Yuanjing Xiao‚ Junliang Zhang*
RhI-Catalyzed Regio- and Stereospecific Carbonylation of 1-(1-Alkynyl)cyclopropyl Ketones: A Modular Entry to Highly Substituted 5‚6-Dihydrocyclopenta[c]furan-4-ones. Chem. Eur. J.2009‚ 15‚ 5208-5211.
http://www3.interscience.wiley.com/cgi-bin/fulltext/122314633/PDFSTART
5. Yuanjing Xiao‚ Junliang Zhang*
Palladium(II)-Catalyzed Domino Reaction of 2-(1-Alkynyl)-2-alken-1-ones with Nucleophiles: Scope‚ Mechanism and Synthetic Application in the Synthesis of 3‚4-Fused Bicyclic Tetrasubstituted Furans. Adv. Synth. Catal.2009‚ 351‚ 617.
http://www3.interscience.wiley.com/cgi-bin/fulltext/122208194/PDFSTART
4. Hongyin Gao‚ Junliang Zhang*
A Dramatic Substituent Effect in Silver(I)-Catalyzed Regioselective Cyclization of ortho-Alkynylaryl Aldehyde Oxime DerivativesAdv. Synth. Catal. 2009‚ 351‚ 85.
http://www3.interscience.wiley.com/cgi-bin/fulltext/121578716/PDFSTART
3. Liyan Fan‚ Wanxiang Zhao‚ Weihua Jiang‚ Junliang Zhang*
One-Pot Synthesis of Fused Tricyclic Heterocycles with Quaternary Carbon Stereocenter by Sequential Pauson-Khand Reaction and Formal [3+3] Cycloaddition . Chem. Eur. J. 2008‚ 14‚ 9139-9142
http://www3.interscience.wiley.com/cgi-bin/fulltext/121402436/PDFSTART
2. Xiuzhao Yu‚ Hongjun Ren‚ Yuanjing Xiao‚ Junliang Zhang*Efficient Assembly of Allenes‚ 1‚3-Dienes‚ and 4H-Pyrans by Catalytic Regioselective Nucleophilic Addition to Electron-Deficient 1‚3-Conjugated Enynes . Chem. Eur. J.2008‚ 14‚ 8481-8485http://www3.interscience.wiley.com/cgi-bin/fulltext/121372166/PDFSTART
1.Yuanjing Xiao and Junliang Zhang*
Tetrasubstituted Furans by a PdII-Catalyzed Three- Component Michael Addition/Cyclization/Cross-Coupling Reaction. Angew. Chem.‚ Int. Ed. 2008‚ 47‚ 1903-1906.
http://www3.interscience.wiley.com/cgi-bin/fulltext/117902009/PDFSTART
![Graphical abstract:Kinetic resolution of 1-(1-alkynyl)cyclopropyl ketones by gold(i)-catalyzed asymmetric [4+3]cycloaddition with nitrones:scope, mechanism and applications](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CC30309D "Graphical abstract")
![Graphical abstract:Ni(ClO4)2-catalysed regio- and diastereoselective [3+2] cycloaddition of indoles and aryl oxiranyl-dicarboxylates/diketones:a facile access to furo[3,4-b]indoles](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CC16918E "Graphical abstract")
![Graphical abstract:A gold(i)-catalyzed intramolecular oxidation–cyclopropanation sequence of 1,6-enynes:a convenient access to [n.1.0]bicycloalkanes](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C1CC14788A "Graphical abstract")
![Graphical abstract:Nickel(ii)-catalyzed diastereoselective [3+2] cycloaddition of N-tosyl-aziridines and aldehydes via selective carbon–carbon bond cleavage](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C1CC12189H "Graphical abstract")
![Graphical abstract:Lewis acid-catalyzed formal [3+2] cycloadditions of N-tosyl aziridines with electron-rich alkenes via selective carbon–carbon bond cleavage](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C1CC10926J "Graphical abstract")
![Graphical abstract:Highly regioselective Lewis acid-catalyzed [3+2] cycloaddition of alkynes with donor–acceptor oxiranes by selective carbon–carbon bond cleavage of epoxides](http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C1CC15669A "Graphical abstract")