部分科研成果
2024:
132. Yang Wang, Ji-Chen Yin, Yu-Wei Zhang, Yuzhe Zhang, Feng Shi*, Hypervalent iodine-mediated regioselective dearomatization of non-activated arenes, Adv. Synth. Catal. 2024, DOI: 10.1002/adsc.202400852
131. Cheng-Cheng Tian, Dan Yang, Yu Liu, Wei Chen, Yuzhe Zhang* and Hong-Hao Zhang*, Synthesis of β-Amino Acid Derivatives via Photoredox-Catalyzed Radical Cross‐Coupling of Anilines with Diazo Compounds. Org. Chem. Front. 2024,
DOI: 10.1039/D4QO01396D
130. Tian-Zhen Li, Shu-Fang Wu, Ning-Yi Wang, Chen-Shengping Hong, Yu-Chen Zhang,* and Feng Shi*, Catalytic Atroposelective Synthesis of N−N Axially Chiral Indolylamides. J. Org. Chem. 2024, DOI: 10.1021/acs.joc.4c01489
129. Ping Wu, Wen-Tao Zhang, Ji-Xiang Yang, Xian-Yang Yu, Shao-Fei Ni,* Wei Tan* and Feng Shi*, Synthesis of Alkene Atropisomers with Multiple Stereogenic Elements via Catalytic Asymmetric Rearrangement of 3- Indolylmethanols. Angew. Chem. Int. Ed. 2024, e202410581, DOI: 10.1002/anie.202410581
128. Wei Tan,* Xin-Yue Wu, and Feng Shi*, Catalytic Atroposelective Construction of Furan-Based Axially Chiral Scaffolds. ChemCatChem 2024, DOI: 10.1002/cctc.202401022
127.Si-Jia Liu, Tian-Zhen Li, Ning-Yi Wang, Qi Cheng, Yinchun Jiao,* Yu-Chen Zhang,* and Feng Shi*, Catalytic Asymmetric Formal (2 + 3) Cycloaddition Involving Methyl-Substituted 2-Indolylmethanols, Org. Chem. Front. 2024, DOI: 10.1039/D4QO01047G
126. Yue Wang, Jiang-Ning Yu, Yang Wang,* and Feng Shi*, Intermolecular α‑Functionalization of Benzylamides with N‑Nucleophiles via Oxidative Umpolung: Synthesis of Tetrasubstituted 3,3′-Oxindoles, Org. Lett. 2024, DOI:10.1021/acs.orglett.4c02167
125. Bo-Wen Lai, Shi-Yu Qu, Yu-Xian Yin, Rui Li, Kuiyong Dong*, and Feng Shi*, Cooperative Catalysis-Enabled (4 + 3) Cycloaddition of 2-Indolylmethanols with In Situ-Generated ortho-Naphthoquinone Methides, J. Org. Chem. 2024, 89(14), 10197–10211. DOI: 10.1021/acs.joc.4c01080
124.Zi-Qi Zhu,* Tian-Zhen Li, Si-Jia Liu, and Feng Shi*, Advances in Organocatalytic Asymmetric [3+3] Cycloadditions Synthesis of Chiral Six-Membered (Hetero)cyclic Compounds, Org. Chem. Front. 2024, DOI: 10.1039/D4QO00515E
123. Shuang Yang, Jia-Bo Huang, Da-Hua Wang, Ning-Yi Wang, Yu-Yu Chen, Xin-Yan Ke, Hao Chen, Shao-Fei Ni,* Yu-Chen Zhang,* and Feng Shi*, Catalytic Asymmetric Diastereodivergent Synthesis of 2‑Alkenylindoles Bearing both Axial and Central Chirality. Precis. Chem. 2024, 2(5), 208–220. DOI: 10.1021/prechem.4c00008
122.Tian-Zhen Li, Si-Jia Liu, Shu-Fang Wu, Qi Cheng, Qun Chen,* Yinchun Jiao,* Yu-Chen Zhang* & Feng Shi*, Catalytic Asymmetric (3 + 3) Cycloaddition between Different 2-Indolylmethanols, Science China Chemistry 2024, DOI:10.1007/s11426-023-1927-3
121. Jing-Yi Wang, Cong-Hui Gao, Cheng Ma, Xin-Yue Wu, Shao-Fei Ni,* Wei Tan* and Feng Shi*, Design and Catalytic Asymmetric Synthesis of Furan-Indole Compounds Bearing both Axial and Central Chirality. Angew. Chem., Int. Ed. 2024, 63 e202316454. DOI: 10.1002/anie.202316454
120. Hong-Hao Zhang,* Tian-Zhen Li, Si-Jia Liu, and Feng Shi*, Catalytic Asymmetric Synthesis of Atropisomers Bearing Multipl Chiral Elements: An Emerging Field, Angew. Chem., Int. Ed. 2024, 63, e202311053. DOI: 10.1002/anie.202311053
2023:
119. Shu-Fang Wu, Guo-Ke Zhang, Xue Wang, Zhuo-Jing He, Yu-Chen Zhang,* and Feng Shi*, Organocatalytic Diastereoselective (4 + 1) Cycloaddition of o‑Hydroxyphenyl-Substituted Secondary Phosphine Oxides, J. Org. Chem. 2023, 88(23), 16497-16510. DOI: 10.1021/acs.joc.3c01990
118. Guo-Ke Zhang, Shu-Fang Wu, Chen Zhong, Yu-Qi Liu, Da-Hua Wang*, Yu-Chen Zhang*and Feng Shi*, Copper-Catalyzed α,β-Regioselective (2+4) Cycloaddition of Propargylic Esters, Eur. J. Org. Chem. 2023, 26(46), e202300802. DOI:10.1002/ejoc.202300802
117. Lei Yu, Ran Xu, Yan-Yi Yao, Yu Lu, Fei-Yang Liu, Wei Tan* and Feng Shi*, Organocatalytic (Z/E)‑Selective Synthesis of 3‑Vinylnaphthofurans via a Formal (3 + 2) Cycloaddition, J. Org. Chem. 2023, 88(6), 3474−3486. DOI:10.1021/acs.joc.2c02641
116. Cong-Hui Gao, Lei Yu, Xin-Yue Wu, Hong-Lin Wan, Wei Tan* and Feng Shi*, Brønsted Acid–Catalyzed Tandem Reaction of 1,4-Enediones with 2-Naphthols: Synthesis of 2-Furylmethylnaphthalenes, Asian J. Org. Chem. 2023, 12(9), e202300231. DOI:10.1002/ajoc.202300231
115. Shuang Yang, Ning-yi Wang, Qing-qing Hang, Yu-chen Zhang*, Feng Shi*, Advances in Catalytic Asymmetric Reactions Involving o-Hydroxyphenyl Substituted p-Quinone Methides, Acta Chim. Sinica 2023, 81(7), 793-808. DOI:10.6023/A23040192
114. Jia-Yi Zhang, Jia-Yi Chen, Cong-Hui Gao, Lei Yu, Shao-Fei Ni*, Wei Tan* and Feng Shi*, Asymmetric (4+n) Cycloadditions of Indolyldimethanols for the Synthesis of Enantioenriched Indole-Fused Rings, Angew. Chem. Int. Ed. 2023, 62(37), e202305450. DOI:10.1002/anie.202305450
113. Hai-Qing Wang‡, Shuang Yang‡, Yu-Chen Zhang*, Feng Shi*, Advances in Catalytic Asymmetric Reactions Involving o-Hydroxybenzyl Alcohols, Chin. J. Org. Chem. 2023, 43(3), 974-999. DOI:10.6023/cjoc202211022
112. Zhi-Han Chen‡, Tian-Zhen Li‡, Ning-Yi Wang, Xiao-Fang Ma, Shao-Fei Ni, Yu-Chen Zhang* and Feng Shi*, Organocatalytic Enantioselective Synthesis of Axially Chiral N, N'-Bisindoles, Angew. Chem. Int. Ed. 2023, 62(15), e202300419. DOI:10.1002/anie.202300419
111. Wei Tan*, Jia-Yi Zhang, Cong-Hui Gao, Feng Shi*, Progress in Organocatalytic Asymmetric (4 + 3) Cycloadditions for theEnantioselective Construction of Seven-membered Rings, Sci. China Chem. 2023, 66, 966-992. DOI:10.1007/s11426-022-1471-2
110. Hai-Qing Wang§, Shu-Fang Wu§, Jun-Ru Yang, Yu-Chen Zhang*, and Feng Shi*, Design and Organocatalytic Asymmetric Synthesis of Indolyl-Pyrroloindoles Bearing Both Axial and Central Chirality, J. Org. Chem. 2023, 88(12), 7684–7702. DOI:10.1021/acs.joc.2c02303
109. Yi-Cheng Shi, Xin-Yu Yan, Ping Wu, Song Jiang, Ran Xu, Wei Tan* and Feng Shi*, Design and Application of m-Hydroxybenzyl Alcohols in Regioselective (3+3) Cycloadditions of 2-Indolymethanols, Chin. J. Chem. 2023, 41(1), 27-36. DOI:10.1002/cjoc.202200503
108. Ping Wu, Lei Yu, Cong-Hui Gao, Qi Cheng, Shuang Deng, Yinchun Jiao*, Wei Tan* and Feng Shi*, Design and Synthesis of Axially Chiral Aryl-Pyrroloindoles via the Strategy of Organocatalytic Asymmetric (2+3) Cyclization, Fundam. Res. 2023, 3(2), 237-248. DOI:10.1016/j.fmre.2022.01.002
2022:
107. Hong-Hao Zhang and Feng Shi*, Advances in Catalytic Asymmetric Reactions Using 2-Indolylmethanols as Platform Molecules, Chin. J. Org. Chem. 2022, 42(10), 3351-3372. DOI:10.6023/cjoc202203018
106. Yang Wang*, Zheng-Guang Wu, Feng Shi*, Advances in catalytic enantioselective synthesis of chiral helicenes and helicenoids, Chem. Catalysis 2022, 2(11), 3077-3111. DOI:10.1016/j.checat.2022.10.011
105. Hong-Hao Zhang and Feng Shi*, Organocatalytic Atroposelective Synthesis of Indole Derivatives Bearing Axial Chirality: Strategies and Applications, Acc. Chem. Res. 2022, 55(18), 2562-2580. DOI:10.1021/acs.accounts.2c00465
104. Shuang Yang, Hai-Qing Wang, Jun-Nan Gao, Wen-Xin Tan, Yu-Chen Zhang*, Feng Shi*, Lewis Acid-Catalyzed (3+2) Cycloaddition of 2-Indolylmethanol with β,γ-Unsaturated α-Ketoesters, Eur. J. Org. Chem. 2022, 2022(35), e202200878. DOI:10.1002/ejoc.202200878
103. Qing-Qing Hang†, Shu-Fang Wu†, Shuang Yang, Xue Wang, Zhen Zhong, Yu-Chen Zhang* & Feng Shi*, Design and Catalytic Atroposelective Synthesis of Axially Chira Isochromenone-Indoles, Science China Chemistry 2022, 65, 1929-1937. DOI:10.1007/s11426-022-1363-y
102. Feng-Tao Sheng, Shuang Yang, Shu-Fang Wu, Yu-Chen Zhang*, Feng Shi*, Catalytic Asymmetric Synthesis of Axially Chiral 3,3'-Bisindoles by Direct Coupling of Indole Rings, Chin. J. Chem. 2022, 40(18), 2151-2160. DOI: 10.1002/cjoc.202200327
101. Jing-Yi Wang, Shuming Zhang, Xian-Yang Yu, Yu-Hao Wang, Hong-Lin Wan, Shu Zhang*, Wei Tan*, Feng Shi*, Organocatalytic Asymmetric Synthesis of Bioactive Hexahydropyrrolo[2,3-b] Indole-containing Tetrasubstituted Allenes Bearing Multiple Chiral Elements, Tetrahedron Chem. 2022, 1, 100007. DOI: 10.1016/j.tchem.2022.100007
100. Ke-Wei Chen, Zhi-Han Chen, Shuang Yang, Shu-Fang Wu, Yu-Chen Zhang* and Feng Shi*, Organocatalytic Atroposelective Synthesis of N–N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation, Angew. Chem. Int. Ed. 2022, 61(17), e202116829. DOI:10.1002/anie.202116829
99. Si-Jia Liu, Zhi-Han Chen, Jia-Yi Chen, Shao-Fei Ni*, Yu-Chen Zhang* and Feng Shi*, Rational Design of Axially Chiral Styrene-Based Organocatalysts and Their Application in Catalytic Asymmetric (2+4) Cyclizations, Angew. Chem. Int. Ed. 2022, 61(7), e202112226. DOI:10.1002/anie.202112226
2021:
98. Jing-Yi Wang, Meng Sun, Xian-Yang Yu, Yu-Chen Zhang, Wei Tan* and Feng Shi*, Atroposelective Construction of Axially Chiral Alkene‐Indole Scaffolds via Catalytic Enantioselective Addition Reaction of 3‐Alkynyl‐2‐indolylmethanols, Chin. J. Chem. 2021, 39, 2163-2171. DOI:10.1002/cjoc.202100214
97. Man-Su Tu, Ke-Wei Chen, Ping Wu, Yu-Chen Zhang*, Xiao-Qin Liu* and Feng Shi*, Advances in organocatalytic asymmetric reactions of vinylindoles: powerful access to enantioenriched indole derivatives, Org. Chem. Front. 2021, 8, 2643-2672. DOI: 10.1039/d0qo01643h
96. Tian-Zhen Li, Si-Jia Liu, Yu-Wen Sun, Shuang Deng, Wei Tan, Yingchun Jiao*, Yu-Chen Zhang* and Feng Shi*, Regio- and Enantioselective (3+3) Cycloaddition of Nitrones with 2-Indolylmethanols Enabled by Cooperative Organocatalysis, Angew. Chem. Int. Ed. 2021, 60(5), 2355-2363. DOI:10.1002/anie.202011267
95. Xiao Wan, Meng Sun, Jing-Yi Wang, Lei Yu, Qiong Wu*, Yu-Chen Zhang* and Feng Shi*, Regio- and Enantioselective Ring-Opening Reaction of Vinylcyclopropanes with Indoles under Cooperative Catalysis, Org. Chem. Front. 2021, 8, 212-223. DOI:10.1039/d0qo00699h
2020:
94. Feng-Tao Sheng, Jing-Yi Wang, Wei Tan*, Yu-Chen Zhang* and Feng Shi*, Progresses in Organocatalytic Asymmetric Dearomatization Reactions of Indole Derivatives, Org. Chem. Front. 2020, 7, 3967-3998. DOI:10.1039/D0QO01124J
93. Chun Ma, Feng-Tao Sheng, Hai-Qing Wang, Shuang Deng, Yu-Chen Zhang*, Yin-Chun Jiao, Wei Tan* and Feng Shi*, Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution, J. Am. Chem. Soc. 2020, 142(37), 15686-15696. DOI: 10.1021/jacs.0c00208
92. Ji Zhou, Tian-Zhen Li, Yu-Wen Sun, Bai-Xiang Du, Wei Tan* and Feng Shi*, Chiral Brønsted Acid-Catalyzed Asymmetric 1,4-Addition of Benzofuran-Derived Azadienes with 3-Substituted Indoles, ChemCatChem 2020, 12(19), 4862-4870. DOI: 10.1002/cctc.202000810
91. Ye-Xin Wang, Yi-Nan Lu, Lin-Lin Xu, Feng-Tao Sheng, Jin-Peng Zhang*, Wei Tan* and Feng Shi*, Application of Benzofuran-Derived Azadienes as Two-Carbon Building Blocks in Annulations: Chemo- and Diastereoselective Construction of Spiro-Benzofuran Scaffolds, Synthesis 2020, 52(20), 2979-2986. DOI: 10.1055/s-0040-1707205
90. Ke-Wei Chen, Zhao-Shan Wang, Ping Wu, Xin-Yu Yan, Shu Zhang*, Yu-Chen Zhang* and Feng Shi*, Catalytic Asymmetric Synthesis of 3,3’-Bisindoles Bearing Single Axial Chirality, J. Org. Chem. 2020, 85(15), 10152-10166. DOI: 10.1021/acs.joc.0c01528
89. Si-Jia Zhou, Meng Sun, Jing-Yi Wang, Xian-Yang Yu, Han Lu, Yu-Chen Zhang* and Feng Shi*, Metal-Catalyzed Regiospecific (4+3) Cyclization of 2-Indolylmethanols with ortho-Quinone Methides, Eur. J. Org. Chem. 2020, 2020(28), 4301-4308. DOI: 10.1002/ejoc.202000693
88. Qing-Qing Hang, Si-Jia Liu, Lei Yu, Ting-Ting Sun, Yu-Chen Zhang*, Guang-Jian Mei* and Feng Shi*, Design and Application of Indole-Based Allylic Donors for Pd‐Catalyzed Decarboxylative Allylation Reactions, Chin. J. Chem. 2020, 38(12), 1612-1618. DOI: 10.1002/cjoc.202000104
87. Tian-Zhen Li, Si-Jia Liu, Wei Tan* and Feng Shi*, Catalytic Asymmetric Construction of Axially Chiral Indole-Based Frameworks: An Emerging Area, Chem. Eur. J. 2020, 26(68), 15779-15792. DOI: 10.1002/chem.202001397
86. Cong-Shuai Wang, Tian-Zhen Li, Si-Jia Liu, Yu-Chen Zhang,Shuang Deng, Yinchun Jiao* and Feng Shi*, Axially Chiral Aryl-Alkene-Indole Framework: A Nascent Member of the Atropisomeric Family and Its Catalytic Asymmetric Construction, Chin. J. Chem. 2020, 38, 543-552. DOI: 10.1002/cjoc.202000131
85. Feng-Tao Sheng, Zhi-Min Li, Yi-Zhu Zhang, Li-Xing Sun, Yu-Chen Zhang, Wei Tan*, Feng Shi*, Atroposelective Synthesis of 3,3’-Bisindoles Bearing Axial and Central Chirality: Using Isatin-Derived Imines as Electrophiles, Chin. J. Chem. 2020, 38, 583-589. DOI: 10.1002/cjoc.202000022
84. Yu-Chen Zhang, Fei Jiang, Feng Shi*, Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach, Acc. Chem. Res. 2020, 53(2), 425-446. DOI: 10.1021/acs.accounts.9b00549
2019:
83. Fei Jiang, Ke-Wei Chen, Ping Wu, Yu-Chen Zhang*, Yinchun Jiao, Feng Shi*, A Strategy for Synthesizing Axially Chiral Naphthyl-Indoles: Catalytic Asymmetric Addition Reactions of Racemic Substrates, Angew. Chem. Int. Ed. 2019, 58 (42), 15104-15110.
82. Meng Sun, Chun Ma, Si-Jia Zhou, Sai-Fan Lou, Jian Xiao, Yinchun Jiao*, Feng Shi*, Catalytic Asymmetric (4+3) Cyclizations of In Situ Generated ortho-Quinone Methides with 2-Indolylmethanols, Angew. Chem. Int. Ed. 2019, 58(26), 8703-8708.
81. Chun Ma, Fei Jiang, Feng-Tao Sheng, Yinchun Jiao, Guang-Jian Mei, Feng Shi*, Design and Catalytic Asymmetric Construction of Axially Chiral 3,3’-Bisindole Skeletons, Angew. Chem., Int. Ed. 2019, 58(10), 3014-3020.
80. Can Li, Cong-Shuai Wang, Tian-Zhen Li, Guang-Jian Mei, Feng Shi*, Brønsted Acid-Catalyzed (4 + 3) Cyclization of N,N’‑Cyclic Azomethine Imines with Isatoic Anhydrides, Org. Lett. 2019, 21(3), 598−602.
79. Meng Sun, Xiao Wan, Si-Jia Zhou, Guang-Jian Mei, Feng Shi*, Iridium and Brøsted acid cooperatively catalyzed chemodivergent and stereoselective reactions of vinyl benzoxazinones with azlactones, Chem. Commun. 2019, 55(9), 1283-1286.
78. Cong-Shuai Wang, Tian-Zhen Li, Yu-Chun Cheng, Ji Zhou, Guang-Jian Mei, Feng Shi*, Catalytic Asymmetric [4+1] Cyclization of Benzofuran-Derived Azadienes with 3-Chlorooxindoles, J. Org. Chem. 2019, 84(6), 3214−3222.
2018:
77. Chun Ma, Jia-Yu Zhou, Yi-Zhu Zhang, Guang-Jian Mei*, Feng Shi*, Catalytic Asymmetric [2+3] Cyclizations of Azlactones with Azonaphthalenes, Angew. Chem., Int. Ed. 2018, 57(19), 5398-5402
76. Fei Jiang, Fu-Ru Yuan, Li-Wen Jin, Guang-Jian Mei*, Feng Shi*, Metal-Catalyzed (4 + 3) Cyclization of Vinyl Aziridines with para-Quinone Methide Derivatives, ACS Catal. 2018, 8(11), 10234–10240
75. Yi-Nan Lu, Chun Ma, Jin-Ping Lan, Caiqiang Zhu, Yu-Jia Mao, Guang-Jian Mei, Shu Zhang*, Feng Shi*, Catalytic enantioselective and regioselective substitution of 2,3-indolyldimethanols with enaminones, Org. Chem. Front. 2018, 5(18), 2657-2667.
74. Jia-Le Wu, Jing-Yi Wang, Ping Wu, Jin-Rong Wang, Guang-Jian Mei, Feng Shi*, Diastereo- and enantioselective construction of chiral cyclopenta[b]indole framework via a catalytic asymmetric tandem cyclization of 2-indolymethanols with 2-naphthols, Org. Chem. Front. 2018, 5(9), 1436-1445.
73. Cong-Shuai Wang, Yu-Chun Cheng, Ji Zhou, Guang-Jian Mei, Shu-Liang Wang*, Feng Shi*, Metal-Catalyzed Oxa-[4+2] Cyclizations of Quinone Methides with Alkynyl Benzyl Alcohols, J. Org. Chem. 2018, 83(22), 13861−13873.
72. Meng Sun, Zi-Qi Zhu, L. Gu, Xiao Wan, Guang-Jian Mei, Feng Shi*, Catalytic Asymmetric Dearomative [3 + 2] Cycloaddition of Electron-Deficient Indoles with All-Carbon 1,3-Dipoles, J. Org. Chem. 2018, 83(4), 2341−2348.
71. Guang-Jian Mei*, Shao-Li Xu, Wen-Qin Zheng, Chen-Yu Bian, Feng Shi*, [4 + 2] Cyclization of para-Quinone Methide Derivatives with Alkynes, J. Org. Chem. 2018, 83(3), 1414−1421.
70. Lin-Zhi Li, Cong-Shuai Wang, Wei-Feng Guo, Guang-Jian Mei*, Feng Shi*, Catalytic Asymmetric [4+2] Cycloaddition of in Situ Generated o‑Quinone Methide Imines with o‑Hydroxystyrenes: Diastereo- and Enantioselective Construction of Tetrahydroquinoline Frameworks, J. Org. Chem. 2018, 83(2), 614−623.
69.Meng-Meng Xu, Hai-Qing Wang, Yu-Jia Mao, Guang-Jian Mei, Shu-Liang Wang, Feng Shi*, Cooperative Catalysis-Enabled Asymmetric alfa-Arylation of Aldehydes Using 2-Indolylmethanols as Arylation Reagents, J. Org. Chem. 2018, 83(9), 5027-5034.
68. Jing-Yi Wang, Ping Wu, Jia-Le Wu, Guang-Jian Mei*, Feng Shi*, Chemodivergent Tandem Cyclizations of 2-Indolylmethanols with Tryptophols: C-N versus C-C Bond Formation, J. Org. Chem. 2018, 83(11), 5931-5946.
67. Can Li, Dan-Ni Xu, Chun Ma, Guang-Jian Mei, Feng Shi*, Diastereo- and Enantioselective Construction of Dihydrobenzo[e]indole Scaffolds via Catalytic Asymmetric [3+2] Cycloannulations, J. Org. Chem. 2018, 83(16), 9190-9200.
66. Fei Jiang, Gui-Zhen Luo, Zi-Qi Zhu, Cong-Shuai Wang, Guang-Jian Mei, Feng Shi*, Application of Naphthylindole-Derived Phosphines as Organocatalysts in [4 + 1] Cyclizations of o-Quinone Methides with Morita-Baylis-Hillman Carbonates, J. Org. Chem. 2018, 83(17), 10060-10069.
65. Cong-Shuai Wang, Jia-Le Wu, Can Li, Lin-Zhi Li, Guang-Jian Mei, Feng Shi*, Design of C3-Alkenyl-Substituted 2-Indolylmethanols for Catalytic Asymmetric Interrupted Nazarov-Type Cyclization, Adv. Synth. Catal. 2018, 360(5), 846-851.
64. Ting Zhang, Chun Ma, Jia-Yu Zhou, Guang-Jian Mei, Feng Shi*, Application of Homophthalic Anhydrides as 2C Building Blocks in Catalytic Asymmetric Cyclizations of ortho-Quinone Methides: Diastereo- and Enantioselective Construction of Dihydrocoumarin Frameworks, Adv. Synth. Catal. 2018, 360(6), 1128-1137.
63. Hai-Qing Wang, Meng-Meng Xu, Ying Wan, Yu-Jia Mao, Guang-Jian Mei*, Feng Shi*, Application of 7-Indolylmethanols in Catalytic Asymmetric Arylations with Tryptamines: Enantioselective Synthesis of 7-indolylmethanes, Adv. Synth. Catal. 2018, 360(9), 1850-1860.
62. Zi-Qi Zhu, Lei Yu, Meng Sun, Guang-Jian Mei*, Feng Shi*, Regioselective [3+3] Cyclization of 2-Indolymethanols with Vinylcyclopropanes via Metal Catalysis, Adv. Synth. Catal. 2018, 360(16), 3109-3116.
61. Xiao-Li Jiang, Shu-Fang Wu, Jin-Rong Wang, Guang-Jian Mei, Feng Shi*, Catalytic Asymmetric [4+2] Cyclization of para-Quinone Methide Derivatives with 3-Alkyl-2-vinylindoles Adv. Synth. Catal. 2018, 360(21), 4225-4235.
60. Yi-Nan Lu, Jin-Ping Lan, Yu-Jia Mao, Ye-Xin Wang, Guang-Jian Mei*, Feng Shi*, Catalytic Asymmetric de novo Construction of Dihydroquinazolinone Scaffolds via Enantioselective Decarboxylative [4+2] Cycloadditions, Chem. Commun. 2018, 54(96), 13527-13530.
59. Guang-Jian Mei, Feng Shi*, Catalytic asymmetric synthesis of spirooxindoles: recent developments, Chem. Commun. 2018, 54(50), 6607-6621. (invited feature article)
58. Chun Ma, Jia-Yu Zhou, Yi-Zhu Zhang, Yinchun Jiao, Guang-Jian Mei, Feng Shi*, Synergistic-Catalysis-Enabled Reaction of 2-Indolymethanols with Oxonium Ylides for the Construction of 3-Indolyl-3-Alkoxy Oxindole Frameworks, Chemistry - An Asian Journal, 2018, 13(17), 2549-2558. (invited)
2017：
57. Hong-Hao Zhang, Cong-Shuai Wang, Can Li, Guang-Jian Mei, Yuxue Li*, Feng Shi*, Design and Enantioselective Construction of Axially Chiral Naphthyl-Indole Skeletons, Angew. Chem., Int. Ed. 2017, 56(1), 116 –121.
56. Fei Jiang, Dan Zhao, Xue Yang, Fu-Ru Yuan, Guang-Jian Mei, Feng Shi*, Catalyst-Controlled Chemoselective and Enantioselective Reactions of Tryptophols with Isatin-Derived Imines, ACS Catal. 2017, 7(10), 6984-6989.
55. Chun Ma, Ting Zhang, Jia-Yu Zhou, Guang-Jian Mei, Feng Shi*, Catalytic asymmetric chemodivergent arylative dearomatization of tryptophols, Chem. Commun. 2017, 53(89), 12124-12127.
54. Guang-Jian Mei, Zi-Qi Zhu, Jia-Jia Zhao, Chen-Yu Bian, Jie Chen, Ruo-Wei Chen, Feng Shi*, Brønsted acid-catalyzed stereoselective [4+3] cycloadditions of ortho-hydroxybenzyl alcohols with N,N’-cyclic azomethine imines, Chem. Commun. 2017, 53(18), 2768-2771.
53. Guang-Jian Mei, Zi-Qi Zhu, Jia-Jia Zhao, Chen-Yu Bian, Jie Chen, Ruo-Wei Chen, Feng Shi*, A catalytic asymmetric construction of a tetrahydroquinoline-based spirooxindole framework via a diastereoand enantioselective decarboxylative [4+2] cycloaddition, Chem. Commun. 2017, 53(72), 10030-10033.
52. Guang-Jian Mei*, Chen-Yu Bian, Guo-Hao Li, Shao-Li Xu, Wen-Qin Zheng, and Feng Shi*, Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization, Org. Lett. 2017, 19(12), 3219-3222.
51. Zi-Qi Zhu, Yang Shen, Jin-Xi Liu, Ji-Yu Tao, and Feng Shi*, Enantioselective Direct α‑Arylation of Pyrazol-5-ones with 2‑Indolylmethanols via Organo-Metal Cooperative Catalysis, Org. Lett. 2017, 19(7), 1542-1545.
50. Meng-Meng Xu, Hai-Qing Wang, Ying Wan, Guofeng He, Jingjing Yan, Shu Zhang*, Shu-Liang Wang, Feng Shi*, Catalytic asymmetric substitution of orthohydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes, Org. Chem. Front. 2017, 4(3), 358-368.
49. Zi-Qi Zhu, Lei Yin, Yang Wang, Yang Shen, Can Li, Guang-Jian Mei*, Feng Shi*, Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles, Org. Chem. Front. 2017, 4(1), 57–68.
48. Jia-Le Wu, Jing-Yi Wang, Ping Wu, Guang-Jian Mei, Feng Shi*, Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols, Org. Chem. Front. 2017, 4(12), 2465-2479.
47. Ying-Ying He, Xiao-Xue Sun, Guo-Hao Li, Guang-Jian Mei*, Feng Shi*, Substrate-Controlled Regioselective Arylations of 2-Indolylmethanols with Indoles: Synthesis of Bis(indolyl)methane and 3,3'-Bisindole Derivatives, J. Org. Chem. 2017, 82(5), 2462-2471.
46. Guang-Jian Mei, Feng Shi*, Indolylmethanols as Reactants in Catalytic Asymmetric Reactions, J. Org. Chem. 2017, 82(15), 7695-7707. (invited Synopsis)
45. Meng-Meng Xu, Hai-Qing Wang, Ying Wan, Shu-Liang Wang, Feng Shi*, Enantioselective Construction of Cyclopenta[b]indole Scaffolds via the Catalytic Asymmetric [3 + 2] Cycloaddition of 2-Indolylmethanols with p-Hydroxystyrenes, J. Org. Chem. 2017, 82(19), 10226-10233.
44. Xiao-Xue Sun, Can Li, Ying-Ying He, Zi-Qi Zhu, Guang-Jian Mei, Feng Shi*, Catalytic Asymmetric [3+3] Cycloaddition of Azomethine Ylides with C3-Substituted 2-Indolylmethanols, Adv. Synth. Catal. 2017, 359(15), 2660-2670.
43. Xiao-Li Jiang, Si-Jia Liu, Yu-Qi Gu, Guang-Jian Mei*, Feng Shi*, Catalytic Asymmetric [4+1] Cyclization of ortho-Quinone Methides with 3-Chlorooxindoles, Adv. Synth. Catal. 2017, 359(19), 3341-3346.
2016：
42. Jia-Jia Zhao, Man Tang, Hong-Hao Zhang, Meng-Meng Xu, Feng Shi*, Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation, Chem. Commun. 2016, 52(35), 5953-5956.
41. Xiao-Xue Sun, Hong-Hao Zhang, Guo-Hao Li, Meng, Li; Feng Shi*, Diastereo- and enantioselective construction of an indole-based 2,3-dihydrobenzofuran scaffold via catalytic asymmetric [3+2] cyclizations of quinone monoimides with 3-vinylindoles, Chem. Commun. 2016, 52(14), 2968-2971.
40. Yue-Ming Wang, Hong-Hao Zhang, Can Li, Tao Fan, Feng Shi*, Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3'-oxindole] framework, Chem. Commun. 2016, 52(9), 1804-1807.
39. Cong-Shuai Wang, Tao Fan, Hong-Hao Zhang, Can Li, Yang Shen, Guang-Jian Mei*, Feng Shi*, Gallium Bromide-Promoted Dearomative Indole Insertion in 3-Indolylmethanols: Chemoselective and (Z/E)-Selective Synthesis of 3,3'-Bisindole Derivatives, J. Org. Chem. 2016, 81(23), 11734-11742.
38. Yu-Chen Zhang, Qiu-Ning Zhu, Xue Yang, Lu-Jia Zhou, Feng Shi*, Merging Chiral Bronsted Acid/Base Catalysis: An Enantioselective [4 + 2] Cycloaddition of o-Hydroxystyrenes with Azlactones, J. Org. Chem. 2016, 81(4), 1681-1688.
37. Jia-Le Wu, Bai-Xiang Du, Yu-Chen Zhang, Ying-Ying He, Jing-Yi Wang, Ping Wu, Feng Shi*, Diastereo- and Enantioselective Construction of Dihydroisocoumarin-Based Spirooxindole Frameworks via Organocatalytic Tandem Reactions, Adv. Synth. Catal. 2016, 358(17), 2777-2790.
36. Lei Yin, Yang Wang, Meng Sun, Feng Shi*, Bronsted Acid-Catalyzed [3+2] Cyclodimerization of 3-Alkyl- 2-vinylindoles Leading to the Diastereoselective Construction of a Pyrroloindole Framework, Adv. Synth. Catal. 2016, 358(7), 1093-1102.
35. Tao Fan, Hong-Hao Zhang, Can Li, Yang Shen, Feng Shi*, The Application of N-Protected 3-Vinylindoles in Chiral Phosphoric Acid-Catalyzed [3+2] Cyclization with 3-Indolylmethanols: Monoactivation of the Catalyst to Vinyliminium, Adv. Synth. Catal. 2016, 358(12), 2017-2031.
34.Lu-Jia Zhou, Yu-Chen Zhang, Fei Jiang, Guofeng He, Jingjing Yan, Han Lu*; Shu Zhang*; Feng Shi*, Enantioselective Construction of Cyclic Enaminone-Based 3-Substituted 3-Amino-2-oxindole Scaffolds via Catalytic Asymmetric Additions of Isatin-Derived Imines, Adv. Synth. Catal. 2016, 358(19), 3069-3083.
33. Zi-Qi Zhu, Yang Shen, Xiao-Xue Sun, Ji-Yu Tao, Jin-Xi Liu, Feng Shi*, Catalytic Asymmetric [3+2] Cycloadditions of C-3 Unsubstituted 2-Indolylmethanols: Regio-, Diastereo- and Enantioselective Construction of the Cyclopenta[b]indole Framework, Adv. Synth. Catal. 2016, 358(23), 3797-3808.
32. Hong-Hao Zhang, Zi-Qi Zhu, Tao Fan, Jing Liang, Feng Shi*, Intermediate-Dependent Unusual [4+3], [3+2] and Cascade Reactions of 3-Indolylmethanols: Controllable Chemodivergent and Stereoselective Synthesis of Diverse Indole Derivatives, Adv. Synth. Catal. 2016, 358(8), 1259-1288.
31. Xiao-Xue Sun, Hong-Hao Zhang, Guo-Hao Li, Ying-Ying He, Feng Shi*, Catalytic Enantioselective and Regioselective [3+3] Cycloadditions Using 2-Indolylmethanols as 3 C Building Blocks, Chem. Eur. J. 2016, 22(49), 17526-17532.
30. Wei Dai, Xiao-Li Jiang, Ji-Yu Tao, Feng Shi*, Application of 3-Methyl-2-vinylindoles in Catalytic Asymmetric Povarov Reaction: Diastereo- and Enantioselective Synthesis of Indole-Derived Tetrahydroquinolines, J. Org. Chem 2016, 81(1), 185-192.
29. Xue Yang, Yu-Chen Zhang, Qiu-Ning Zhu, Man-Su Tu*, Feng Shi*, Diastereo- and Enantioselective Construction of the Hexahydrocoumarin Scaffold via an Organocatalytic Asymmetric [3 + 3] Cyclization, J. Org. Chem. 2016, 81(12), 5056-5065.
28. Qiu-Ning Zhu, Yu-Chen Zhang, Meng-Meng Xu, Xiao-Xue Sun, Xue Yang, Feng Shi*, Enantioselective Construction of Tetrahydroquinolin-5-one-Based Spirooxindole Scaffold via an Organocatalytic Asymmetric Multicomponent [3 + 3] Cyclization, J. Org. Chem. 2016, 81(17), 7898-7907.
2015：
27. Jia-Jia Zhao, Si-Bing Sun, Sai-Huan He, Qiong Wu, Feng Shi*, Catalytic Asymmetric Inverse-Electron-Demand Oxa-Diels-Alder Reaction of In Situ Generated ortho-Quinone Methides with 3-Methyl-2-Vinylindoles, Angew. Chem., Int. Ed. 2015, 54(18), 5460-5464.
26. Yang Wang, Meng Sun, Lei Yin and Feng Shi*, Catalytic Enantioselective Arylative Dearomatization of 3-Methyl-2-vinylindoles Enabled by Reactivity Switch, Adv. Synth. Catal. 2015, 357(18), 4031-4040.
25. Fei Jiang, Yu-Chen Zhang, Si-Bing Sun, Lu-Jia Zhou, Feng Shi*, Organocatalytic Reactions of Indoles with Quinone Imine Ketals: An Alternative Metal-Free Approach to Bioactive meta-Indolylanilines, Adv. Synth. Catal. 2015, 357(6), 1283-1292.
24. Feng Shi*, Hong-Hao Zhang, Xiao-Xue Sun, Jing Liang, Tao Fan, Shu-Jiang Tu, Organocatalytic Asymmetric Cascade Reactions of 7-Vinylindoles: Diastereo- and Enantioselective Synthesis of C7-Functionalized Indoles, Chem. Eur. J. 2015, 21(8), 3465-3471.
23. Cong-Shuai Wang, Ren-Yi Zhu, Jian Zheng, Feng Shi*, Shu-Jiang Tu, Enantioselective Construction of Spiro[indoline-3,2'-pyrrole] Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions Using Allenes as Equivalents of Alkynes, J. Org. Chem. 2015, 80(1), 512-520.
22. Xin Li, Wei Tan, Yu-Xin Gong, Feng Shi*, Catalyst-Controlled Chemoselective Reaction of 3-Indolylmethanols with Cyclic Enaminones Leading to C2-Functionalized Indoles, J. Org. Chem. 2015, 80(3), 1841-1848.
21. Yang Wang, Man-Su Tu, Lei Yin, Meng Sun, Feng Shi*, Bronsted Acid Catalyzed Asymmetric Diels-Alder Reactions: Stereoselective Construction of Spiro[tetrahydrocarbazole-3,3'-oxindole] Framework, J. Org. Chem. 2015, 80 (6), 3223-3232.
20. Wei Dai, Xiao-Li Jiang, Qiong Wu, Feng Shi*, Shu-Jiang Tu, Diastereo- and Enantioselective Construction of 3,3’-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions, J. Org. Chem. 2015, 80(11), 5737-5744.
18. Cong-Shuai Wang, Ren-Yi Zhu, Yu-Chen Zhang and Feng Shi*, Catalytic Chemoselective [3+3] Cycloadditions of Azomethine Ylides with Quinone Monoimides Leading to the Construction of A Dihydrobenzoxazine Scaffold, Chem. Commun. 2015, 51(59), 11798-11801.
17. Xiao-Xue Sun, Bai-Xiang Du, Hong-Hao Zhang, Lei Ji, Feng Shi*, Catalytic Asymmetric Arylation of 3-Indolylmethanols: Enantioselective Synthesis of 3,3'-Bis(indolyl)oxindoles with High Atom Economy, ChemCatChem. 2015, 7(7), 1211-1221.
2014：
16. Yu-Chen Zhang, Jia-Jia Zhao, Fei Jiang, Si-Bing Sun, Feng Shi*, Organocatalytic Asymmetric Arylative Dearomatization of 2,3-Disubstituted Indoles Enabled by Tandem Reactions, Angew. Chem., Int. Ed. 2014, 53(50), 13912-13915.
15. Yu-Chen Zhang, Fei Jiang, Shu-Liang Wang*, Feng Shi*, Shu-Jiang Tu , Organocatalytic Chemo- and Regioselective Oxyarylation of Styrenes via a Cascade Reaction: Remote Activation of Hydroxyl Groups, J. Org. Chem. 2014, 79(13), 6143-6152.
14. Hong-Hao Zhang, Yue-Ming Wang, Yuan-Wei Xie, Zi-Qi Zhu, Feng Shi*, Shu-Jiang Tu, Organocatalytic Chemo-, (E/Z)- and Enantioselective Formal Alkenylation of Indole-Derived Hydroxylactams Using o-Hydroxystyrenes as a Source of Alkenyl Group, J. Org. Chem. 2014, 79(15), 7141-7151.
13. Ren-Yi Zhu, Cong-Shuai Wang, Jian Zheng, Feng Shi*, Shu-Jiang Tu, Organocatalytic Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of N,N'-Cyclic Azomethine Imines, J. Org. Chem. 2014, 79(19), 9305-9312.
12. Lu-Jia Zhou, Yu-Chen Zhang, Jia-Jia Zhao, Feng Shi*, Shu-Jiang Tu, Organocatalytic Arylation of 3-Indolylmethanols via Chemo- and Regiospecific C6-Functionalization of Indoles, J. Org. Chem. 2014, 79(21), 10390-10398.
11. Yang Wang, Man-Su Tu, Feng Shi*, Shu-Jiang Tu, Enantioselective construction of the biologically significant dibenzo[1,4]diazepine scaffold via organocatalytic asymmetric three-component reactions, Adv. Synth. Catal. 2014, 356(9), 2009-2019.
10. Wei Dai, Han Lu, Xin Li, Feng Shi*, Shu-Jiang Tu, Diastereo- and enantioselective construction of a bispirooxindole scaffold containing a tetrahydro-β-carboline moiety through an organocatalytic asymmetric cascade reaction, Chem. Eur. J. 2014, 20(36), 11382-11389.
9. Feng Shi*, Ren-Yi Zhu, Wei Dai, Cong-Shuai Wang, Shu-Jiang Tu*, Catalytic Asymmetric Formal [3+3] Cycloaddition of an Azomethine Ylide with 3-Indolylmethanol: Enantioselective Construction of a Six-Membered Piperidine Framework, Chem. Eur. J. 2014, 20(9), 2597-2604.
8. Yang Wang, Feng Shi*, Xi-Xi Yao, Meng Sun, Liang Dong, Shu-Jiang Tu, Catalytic Asymmetric Construction of 3,3'-Spirooxindoles Fused with Seven-Membered Rings by Enantioselective Tandem Reactions, Chem. Eur. J. 2014, 20(46), 15047-15052.
7.Yan Liu, Hong-Hao Zhang, Yu-Chen Zhang, Yan Jiang, Feng Shi*, Shu-Jiang Tu, Organocatalytic enantioselective and (Z)-selective allylation of 3-indolylmethanol via hydrogen-bond activation, Chem. Commun. 2014, 50(81), 12054-12057.
6. Wei Tan, Xin Li, Yu-Xin Gong, Meng-Di Ge, Feng Shi*, Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3'-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions, Chem. Commun. 2014, 50(100), 15901-15904.
5. Wei Tan, Bai-Xiang Du, Xin Li, Xu Zhu, Feng Shi*, Shu-Jiang Tu, Catalytic Asymmetric Aza-ene Reaction of 3-Indolylmethanols with Cyclic Enaminones: Enantioselective Approach to C3-Functionalized Indoles, J. Org. Chem. 2014, 79(10), 4635-4643.
2013：
4. Feng Shi*, Gui-Juan Xing, Ren-Yi Zhu, Wei Tan, Shu-jiang Tu*, A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2'-quinoline] Scaffold, Org. Lett. 2013, 15(1), 128-131.
3. Feng Shi*, Ren-Yi Zhu, Xia Liang, Shu-Jiang Tu*, Catalytic Asymmetric 1,3-Dipolar Cycloadditions of Alkynes with Isatin-Derived Azomethine Ylides: Enantioselective Synthesis of Spiro[indoline-3,2'-pyrrole] Derivatives, Adv. Synth. Catal. 2013, 355(11-12), 2447-2458.
2. Feng Shi*, Wei Tan, Hong-Hao Zhang, Mei Li, Qin Ye, Guan-Hua Ma, Shu-Jiang Tu*, Guigen Li, Asymmetric Organocatalytic Tandem Cyclization/Transfer Hydrogenation: A Synthetic Strategy for Enantioenriched Nitrogen Heterocycles, Adv. Synth. Catal. 2013, 355(18), 3715-3726.
1. Feng Shi*, Wei Tan, Ren-Yi Zhu, Gui-Juan Xing, Shu-Jiang Tu*, Catalytic Asymmetric Five-Component Tandem Reaction: Diastereoselective and Enantioselective Synthesis of Densely Functionalized Tetrahydropyridines with Biological Importance, Adv. Synth. Catal. 2013, 355(8), 1605-1622.
