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发表于 2021-3-1 09:22:49
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本帖最后由 gdqqdl 于 2021-3-1 18:54 编辑
游书力你的统计总篇数和上次你的统计一样,但是论文不一样。
WOS已经收录情况看73篇(25篇J+48篇A),有的人WOS没有权限,所以下面我把原文链接贴出来,不需权限。
游书力从2006年起J/A通讯论文76篇
通讯26篇J. Am. Chem. Soc.,50篇Angew.Chem. Int. Ed.
26篇J. Am. Chem. Soc. 1 1 3 3 2 0 3 2 4 2 1 1 2 1 0 1 0
50篇Angew.Chem. Int. Ed. 2 3 6 5 8 5 6 4 1 3 2 3 1 0 0 1
游书力JACS,共30篇,2009年以后通讯直接数*号就有25篇+2007年1篇通讯
https://pubs.acs.org/action/doSearch?field1=Contrib&text1=shu-li+you&publication=&accessType=allContent&Earliest=&earlycite=on&sortBy=Earliest&ContribStored=You%2C+Shu-Li&SeriesKey=jacsat&startPage=0&pageSize=100
1.Journal of the American Chemical Society 2021, 143, 1, 114-120 (Communication) DOI: 10.1021/jacs.0c11735
Qiang Wang, Wen-Wen Zhang, Chao Zheng, Qing Gu, and Shu-Li You*
2.Journal of the American Chemical Society 2020, 142, 45, 19354-19359 (Article) DOI: 10.1021/jacs.0c09638
Ye Wang, Wen-Yun Zhang, Jia-Hao Xie, Zong-Lun Yu, Jia-Hao Tan, Chao Zheng, Xue-Long Hou, and Shu-Li You*
3.Journal of the American Chemical Society 2020, 142, 37, 15678-15685 (Communication) DOI: 10.1021/jacs.0c08205
Qiang Wang, Wen-Wen Zhang, Hao Song, Jian Wang, Chao Zheng, Qing Gu, and Shu-Li You*
4.Journal of the American Chemical Society 2020, 142, 16, 7379-7385 (Communication) DOI: 10.1021/jacs.0c02813
Wen-Jun Cui, Zhi-Jie Wu, Qing Gu, and Shu-Li You*
5.Journal of the American Chemical Society 2019, 141, 24, 9504-9510 (Communication) DOI: 10.1021/jacs.9b03862
Qiang Wang, Zhong-Jian Cai, Chen-Xu Liu, Qing Gu, and Shu-Li You*
6.Journal of the American Chemical Society 2019, 141, 6, 2228-2232 (Communication) DOI: 10.1021/jacs.8b13182
Ye Wang, Wen-Yun Zhang, and Shu-Li You*
7.Journal of the American Chemical Society 2019, 141, 6, 2636-2644 (Article) DOI: 10.1021/jacs.8b12965
Min Zhu, Chao Zheng*, Xiao Zhang*, and Shu-Li You*
8.Journal of the American Chemical Society 2018, 140, 24, 7737-7742 (Article) DOI: 10.1021/jacs.8b05126
Sheng-Biao Tang, Xiao Zhang, Hang-Fei Tu, and Shu-Li You*
9.Journal of the American Chemical Society 2018, 140, 8, 3114-3119 (Article) DOI: 10.1021/jacs.8b00136
Ze-Peng Yang, Ru Jiang, Chao Zheng*, and Shu-Li You*
10.Journal of the American Chemical Society 2016, 138, 18, 5793-5796 (Communication) DOI: 10.1021/jacs.6b02678
Lin Huang, Li-Xin Dai, and Shu-Li You*
11.Journal of the American Chemical Society 2016, 138, 16, 5242-5245 (Communication) DOI: 10.1021/jacs.6b02302
Jun Zheng, Wen-Jun Cui, Chao Zheng, and Shu-Li You*
12.Journal of the American Chemical Society 2016, 138, 8, 2544-2547 (Communication) DOI: 10.1021/jacs.6b00127
De-Wei Gao, Qing Gu, and Shu-Li You*
13.Journal of the American Chemical Society 2015, 137, 50, 15899-15906 (Article) DOI: 10.1021/jacs.5b10440
Ze-Peng Yang, Qing-Feng Wu, Wen Shao, and Shu-Li You*
14.Journal of the American Chemical Society 2015, 137, 15, 4880-4883 (Communication) DOI: 10.1021/jacs.5b01707
Jun Zheng, Shao-Bo Wang, Chao Zheng, and Shu-Li You*
15.Journal of the American Chemical Society 2014, 136, 46, 16251-16259 (Article) DOI: 10.1021/ja5080135
Chao Zheng*, Chun-Xiang Zhuo, and Shu-Li You*
16.Journal of the American Chemical Society 2014, 136, 44, 15469-15472 (Communication) DOI: 10.1021/ja508645j
Ren-Qi Xu, Qing Gu, Wen-Ting Wu, Zhuo-An Zhao, and Shu-Li You*
17.Journal of the American Chemical Society 2014, 136, 18, 6590-6593 (Communication) DOI: 10.1021/ja5028138
Chun-Xiang Zhuo, Yong Zhou, and Shu-Li You*
18.Journal of the American Chemical Society 2014, 136, 13, 4841-4844 (Communication) DOI: 10.1021/ja500444v
De-Wei Gao, Qin Yin, Qing Gu*, and Shu-Li You*
19.Journal of the American Chemical Society 2013, 135, 22, 8169-8172 (Communication) DOI: 10.1021/ja403535a
Chun-Xiang Zhuo, Qing-Feng Wu, Qiang Zhao, Qing-Long Xu, and Shu-Li You*
20.Journal of the American Chemical Society 2013, 135, 1, 86-89 (Communication) DOI: 10.1021/ja311082u
De-Wei Gao, Yan-Chao Shi, Qing Gu*, Zheng-Le Zhao, and Shu-Li You*
21.Journal of the American Chemical Society 2012, 134, 10, 4812-4821 (Article) DOI: 10.1021/ja210923k
Wen-Bo Liu, Chao Zheng, Chun-Xiang Zhuo, Li-Xin Dai, and Shu-Li You*
22.Journal of the American Chemical Society 2011, 133, 46, 19006-19014 (Article) DOI: 10.1021/ja2092954
Ke-Yin Ye, Hu He, Wen-Bo Liu, Li-Xin Dai, Günter Helmchen, and Shu-Li You*
23.Journal of the American Chemical Society 2010, 132, 33, 11418-11419 (Communication) DOI: 10.1021/ja105111n
Qing-Feng Wu, Hu He, Wen-Bo Liu, and Shu-Li You*
24.Journal of the American Chemical Society 2010, 132, 12, 4056-4057 (Communication) DOI: 10.1021/ja100207s
Qing Gu, Zi-Qiang Rong, Chao Zheng, and Shu-Li You*
25.Journal of the American Chemical Society 2009, 131, 24, 8346-8347 (Communication) DOI: 10.1021/ja901384j
Hu He, Wen-Bo Liu, Li-Xin Dai, and Shu-Li You*
26.Journal of the American Chemical Society 2007, 129, 6, 1484-1485 (Communication) DOI: 10.1021/ja067417a
https://pubs.acs.org/doi/10.1021/ja067417a
Qiang Kang, Zhuo-An Zhao, and Shu-Li You*
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China
E-mail: slyou@mail.sioc.ac.cn
Angewandte不像JACS一目了然,需要每篇看原文链接核实Oxidative Indole Dearomatization for Asymmetric Furoindoline Synthesis by a Flavin-Dependent Monooxygenase Involved in the Biosynthesis of Bicyclic Thiopeptide Thiostrepton Zhi Lin,# Yufeng Xue,# Xiaowei Liang, Jian Wang, Shuangjun Lin, Jiang Tao, Shu-Li You,* and Wen Liu*
1.Angewandte Chemie International Edition Accepted Articles First published: 25 January 2021 10.1002/anie.202013174
https://onlinelibrary.wiley.com/doi/epdf/10.1002/anie.202013174
Visible‐Light‐Induced Intramolecular Double Dearomative Cycloaddition of Arenes
Min Zhu, Hao Xu, Xiao Zhang,* Chao Zheng,* and Shu-Li You*
2.Angewandte Chemie International Edition Early View First published: 15 January 2021 10.1002/anie.202016899
https://onlinelibrary.wiley.com/doi/10.1002/anie.202016899
Cheng, Y.-Z.; Huang, X.-L.; Zhuang, W.-H.; Zhao, Q.-R.; Zhang, X.;* Mei, T.-S.;* You, S.-L.*
Intermolecular Dearomatization of Naphthalene Derivatives by Photoredox‐Catalyzed 1,2‐Hydroalkylation.
3.Angew.Chem. Int. Ed. 2020, 59, 18062-18067.
https://onlinelibrary.wiley.com/doi/10.1002/anie.202008358
Rossi-Ashton, J. A.; Clarke, A. K.; Donald, J. R.; Zheng, C.;* Taylor, R. J. K.;* Unsworth, W. P.;* You, S.-L.*
Iridium‐Catalyzed Enantioselective Intermolecular Indole C2‐Allylation.
4.Angew. Chem. Int. Ed. 2020, 59, 7598-7604.
https://onlinelibrary.wiley.com/doi/10.1002/anie.202001956
Liu, X.-J.; Jin, S; Zhang, W.-Y.; Liu, Q.-Q.; Zheng, C.; You, S.-L.*
Sequence‐Dependent Stereodivergent Allylic Alkylation/Fluorination of Acyclic Ketones.
5.Angew. Chem. Int. Ed. 2020, 59, 2039-2043.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201912882
Cheng, Y.-Z.; Zhao, Q.-R.; Zhang, X.;* You, S.-L.*
Asymmetric Dearomatization of Indole Derivatives with N‐Hydroxycarbamates Enabled by Photoredox Catalysis.
6.Angew. Chem. Int. Ed. 2019, 58, 18069-18074.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201911144
Liu, X.-J.; Zheng, C.; Yang, Y.-H.;Jin, S.; You. S.-L.*
Iridium‐Catalyzed Asymmetric Allylic Aromatization Reaction.
7.Angew. Chem. Int. Ed. 2019, 58, 10493-10499.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201904156
Cheng, Q.; Xie, J.-H.; Weng, Y.-C.; You, S.-L.*
Pd-Catalyzed Dearomatization of Anthranils with Vinylcyclopropanes via [4+3] Cyclization Reaction.
8.Angew. Chem. Int. Ed. 2019, 58, 5739-5743.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201901251
Cai, Z.-J.; Liu, C.-X.; Gu, Q.;* Zheng, C.; You, S.-L.* Pd(II)‐Catalyzed Regio‐ and Enantioselective Oxidative C‐H/C‐H Cross‐Coupling Reaction between Ferrocenes and Azoles.
9.Angew. Chem. Int. Ed. 2019, 58, 2149-2153.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201813887
Xia, Z.-L.; Zheng, C.; Liang, X.-W.; Cai, Y.; You, S.-L.*
Manipulation of Spiroindolenine Intermediates for the Enantioselective Synthesis of 3-(Indol-3-yl)pyrrolidines.
10.Angew. Chem. Int. Ed. 2019, 58, 1158-1162.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201812344
Wang, Q.; Gu, Q.; You, S.-L.*
Enantioselective Carbonyl Catalysis Enabled by Chiral Aldehydes.
11.Angew. Chem. Int. Ed. 2019, 58, 6818-6825.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201808700
Yang, Z.-P.; Jiang, R.; Wu, Q.-F.; Huang L.; Zheng, C.;* You, S.-L.*
Iridium‐Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Benzene Derivatives.
12.Angew. Chem. Int. Ed. 2018, 57, 16190-16193.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201810900
Xu-Xu, Q.-F.; Liu, Q.-Q.; Zhang, X.;* You, S.-L.*
Copper‐Catalyzed Ring Opening of Benzofurans and an Enantioselective Hydroamination Cascade.
13.Angew. Chem. Int. Ed. 2018, 57, 15204-15208.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201809003
Cheng, Q.; Zhang, F.; Cai, Y.; Guo, Y.-L.*; You, S.-L.*
Stereodivergent Synthesis of Tetrahydrofuroindoles via Pd-Catalyzed Asymmetric Dearomative Formal [3+2] Cycloaddition Reactions.
14.Angew. Chem. Int. Ed. 2018, 57, 2134-2138.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201711873
Xia, Z.-L.; Zheng, C.*; Wang, S.-G.; You, S.-L.*
Catalytic Asymmetric Dearomatization of Indolyl Dihydropyridines via Enamine Isomerization/Spirocyclization/Transfer Hydrogenation Sequence.
15.Angew. Chem. Int. Ed. 2018, 57, 2653-2656.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201712435
Cai, Z.-J.; Liu, C.-X.; Gu, Q.*; You, S.-L.*
Thioketone-Directed Palladium(II)-Catalyzed C-H Arylation of Ferrocenes with Aryl Boronic Acids.
16.Angew. Chem. Int. Ed. 2018, 57, 1296-1299.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201711451
Wang, Y.; Zheng, C.; You, S.-L.*
Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy.
17.Angew. Chem., Int. Ed. 2017, 56, 15093-15097.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201708419
Huang, L.; Cai, Y.; Zheng, C.; Dai, L.-X.; You, S.-L*.
Iridium-Catalyzed Enantioselective Synthesis of Pyrrole-Annulated Medium-Sized-Ring Compounds.
18.Angew. Chem. Int. Ed. 2017, 56, 10545-10548.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201705068
Xu, R.-Q.; Gu, Q.; You, S.-L.*
Construction of the Benzomesembrine Skeleton: Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of α-Naphthols and Subsequent Aza-Michael Reaction.
19.Angew. Chem. Int. Ed. 2017, 56, 7252-7256.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201703674
Wang, S.-G.; Xia, Z.-L.; Xu, R.-Q.; Liu, X.-J.; Zheng, C.; You, S.-L.*
Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet–Spengler Reaction of Indolyl Dihydropyridines.
20.Angew. Chem. Int. Ed. 2017, 56, 7440-7443.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201703178
Zheng, J.; Wang, S.-B.; Zheng, C.; You, S.-L.*
Asymmetric Synthesis of Spiropyrazolones by Rhodium-Catalyzed C(sp2)−H Functionalization/Annulation Reactions.
21.Angew. Chem. Int. Ed. 2017, 56, 4540-4544.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201700021
Liu, X.-J.; You, S.-L.*
Enantioselective Iridium-Catalyzed Allylic Substitution with 2-Methylpyridines.
22.Angew. Chem. Int. Ed. 2017, 56, 4002-4005.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201700433
Yang, Z.-P.; Zheng, C.; Huang, L.; Qian, C.; You, S.-L.*
Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Benzoxazoles, Benzothiazoles, and Benzimidazoles.
23.Angew. Chem. Int. Ed. 2017, 56, 1530-1534.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201611056
Tu, H.-F.; Zheng, C.; Xu, R.-Q.; Liu, X.-J.; You, S.-L.*
Iridium-Catalyzed Intermolecular Asymmetric Dearomatization of β-Naphthols with Allyl Alcohols or Allyl Ethers.
24.Angew. Chem. Int. Ed. 2017, 56, 3237-3241.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201609654
Xu, R.-Q.; Yang, P.; Tu, H.-F.; Wang, S.-G.; You, S.-L.*
Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of β-Naphthols.
25.Angew. Chem. Int. Ed. 2016, 55, 15137-15141 .
https://onlinelibrary.wiley.com/doi/10.1002/anie.201608724
Wang, D.-C.; Xie, M.-S.; Guo, H.-M.*; Qu, G.-R.; Zhang, M.-C.; You, S.-L.*
Enantioselective Dearomative [3+2] Cycloaddition Reactions of Benzothiazoles.
26.Angew. Chem. Int. Ed. 2016, 55, 14111-14115.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201607852
Ye, K.-Y.; Cheng, Q.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.*
An Iridium(I) N-Heterocyclic Carbene Complex Catalyzes Asymmetric Intramolecular Allylic Amination Reactions.
27.Angew. Chem. Int. Ed. 2016, 55, 8113-8116.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201603266
Cheng, Q.; Wang, Y.; You, S.-L.*
Chemo-, Diastereo-, and Enantioselective Iridium-Catalyzed Allylic Intramolecular Dearomatization Reaction of Naphthol Derivatives.
28.Angew. Chem. Int. Ed. 2016, 55, 3496-3499.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201511519
Liu, C.; Yi, J.-C.; Zheng, Z.-B.; Tang, Y.*; Dai, L.-X.; You, S.-L.*
Enantioselective Synthesis of 3a-Amino-Pyrroloindolines by Copper-Catalyzed Direct Asymmetric Dearomative Amination of Tryptamines.
29.Angew. Chem. Int. Ed. 2016, 55, 751-754.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201508570
Wang, S.-G.; Liu, X.-J.; Zhao, Q.-C.; Zheng, C.; Wang, S.-B.; You, S.-L.*
Asymmetric Dearomatization of β-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction.
30.Angew. Chem. Int. Ed. 2015, 54, 14929-14932.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201507998
Zhuo, C.-X.; Zhou, Y.; Cheng, Q.; Huang, L.; You, S.-L.*
Enantioselective Construction of Spiroindolines with Three Contiguous Stereogenic Centers and Chiral Tryptamine Derivatives via Reactive Spiroindolenine Intermediates.
31.Angew. Chem. Int. Ed. 2015, 54, 14146-14149.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201507193
Zhuo, C.-X.; Chen, Q.; Liu, W.-B.; Zhao, Q.; You, S.-L.*
Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions.
32.Angew. Chem. Int. Ed. 2015, 54, 8475-8479.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201502259
Shao, W.; Li, H.; Liu, C.; Liu, C.-J.*; You, S.-L.*
Copper-Catalyzed Intermolecular Asymmetric Propargylic Dearomatization of Indoles.
33.Angew. Chem. Int. Ed. 2015, 54, 7684-7687.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201503042
Zhang, X.; Yang, Z.-P.; Hang, L.; You, S.-L.*
Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination.
34.Angew. Chem. Int. Ed. 2015, 54, 1873-1876.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201409976
Wang, S.-G.; Yin, Q.; Zhuo, C.-X.; You, S.-L.*
Asymmetric Dearomatization of β-Naphthols through an Amination Reaction Catalyzed by a Chiral Phosphoric Acid.
35.Angew. Chem. Int. Ed. 2015, 54, 647-650.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201409756
Zheng, J.; You, S.-L.*
Construction of Axial Chirality by Rhodium-Catalyzed Asymmetric Dehydrogenative Heck Coupling of Biaryl Compounds with Alkenes.
36.Angew. Chem. Int. Ed. 2014, 53, 13244-13247.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201408805
Yang, Z.-P.; Wu, Q.-F.; You, S.-L.*
Direct Asymmetric Dearomatization of Pyridines and Pyrazines by Iridium-Catalyzed Allylic Amination Reactions.
37.Angew. Chem. Int. Ed. 2014, 53, 6986-6989.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201404286
Li, W.; Liu, C.; Zhang, H.; Ye, K.; Zhang, G.; Zhang, W.; Duan, Z.; You, S.*; Lei, A.*
Palladium-Catalyzed Oxidative Carbonylation ofN-Allylamines for the Synthesis of beta-Lactams.
38.Angew. Chem. Int. Ed. 2014, 53, 2443-2446.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201309081
Wang, S.-G.; You, S.-L.*
Hydrogenative Dearomatization of Pyridine and Asymmetric Aza-Friedel–Crafts Alkylation Sequence.
39.Angew. Chem. Int. Ed. 2014, 53, 2194-2197.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201309876
Zhuo, C.-X.; You, S.-L.*
Palladium-Catalyzed Intermolecular Asymmetric Allylic Dearomatization Reaction of Naphthol Derivatives.
40.Angew. Chem. Int. Ed. 2013, 52, 10056-10059.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201304591
Zhuo, C.-X.; Zhang, W.*; You, S.-L.*
Catalytic Asymmetric Dearomatization Reactions. Angew.
41.Angew. Chem. Int. Ed. 2012, 51, 12662-12686.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201204822
Liu, W.-B.; Zhang, X.; Dai, L.-X.; You, S.-L.*
Asymmetric N-Allylation of Indoles Through the Iridium-Catalyzed Allylic Alkylation/Oxidation of Indolines.
42.Angew. Chem. Int. Ed. 2012, 51, 5183-5187.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201200649
Wu, Q.-F.; Zheng, C.; You, S.-L.*
Enantioselective Synthesis of Spiro Cyclopentane-1,3′-indoles and 2,3,4,9-Tetrahydro-1H-carbazoles by Iridium-Catalyzed Allylic Dearomatization and Stereospecific Migration.
43.Angew. Chem. Int. Ed. 2012, 51, 1680-1683.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201107677
Cai, Q.; Zheng, C.; Zhang, J.-W.; You, S.-L.*
Enantioselective Michael/Mannich Polycyclization Cascade of Indolyl Enones Catalyzed by Quinine-Derived Primary Amines.
44.Angew. Chem. Int. Ed. 2011, 50, 8665-8669.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201103937
Wu, Q.-F.; Liu, W.-B.; Zhuo, C.-X.; Rong, Z.-Q.; Ye, K.-Y.; You, S.-L.*
Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Phenols.
45.Angew. Chem. Int. Ed. 2011, 50, 4455-4458.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201100206
Cai, Q.; Zheng, C.; You, S.-L.*
Enantioselective Intramolecular Aza-Michael Additions of Indoles Catalyzed by Chiral Phosphoric Acids.
46.Angew. Chem. Int. Ed. 2010, 49, 8666-8669.
https://onlinelibrary.wiley.com/doi/10.1002/anie.201003919
Peng, H. M.; Dai, L.-X.; You, S.-L.*
Enantioselective Palladium-Catalyzed Direct Alkylation and Olefination Reaction of Simple Arenes
47.Angew. Chem. Int. Ed. 2010, 49, 5826-5828. (Highlights)
https://onlinelibrary.wiley.com/doi/10.1002/anie.201000799
He, H.; Liu, W.-B.; Dai, L.-X.; You, S.-L.*
Enantioselective Synthesis of 2,3-Dihydro-1H-benzoazepines via Ir-Catalyzed Tandem Allylic Vinylation/Amination Reaction.
48.Angew. Chem. Int. Ed. 2010, 49, 1496-1499.
https://onlinelibrary.wiley.com/doi/10.1002/anie.200906638
Cai, Q.; Zhao, Z.-A.; You, S.-L.*
Asymmetric Construction of Polycyclic Indoles through Olefin Cross-Metathesis/ Intramolecular Friedel-Crafts Alkylation under Sequential Catalysis.
49.Angew. Chem. Int. Ed. 2009, 48, 7428-7431.
https://onlinelibrary.wiley.com/doi/10.1002/anie.200903462
You, S.-L.*; Dai, L.-X.
Enantioselective Palladium-Catalyzed Decarboxylative Allylic Alkylations.
50.Angew. Chem. Int. Ed. 2006, 45, 5246-5248.
https://onlinelibrary.wiley.com/doi/10.1002/anie.200601889
其中Angew. Chem. Int. Ed. 2010, 49, 5826-5828. (Highlights)在WOS检索Document Type:Editorial Material
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