中国及华人学者化学五刊(CR/CSR/ACR/JACS/Angew)二十年发表情况

gdqqdl

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

gdqqdl

刘育2001年以来通讯 J/A Article & Review（每篇都在WOS和论文官网链接核实）
1.Journal of the American Chemical Society  2005, 127, 2, 657-666 (Article) DOI: 10.1021/ja046294w
2.Journal of the American Chemical Society  2007, 129, 35, 10656-10657 (Communication) DOI: 10.1021/ja073882b
3.Journal of the American Chemical Society  2008, 130, 2, 600-605 (Article) DOI: 10.1021/ja075981v
4.Journal of the American Chemical Society  2008, 130, 31, 10431-10439 (Article) DOI: 10.1021/ja802465g
5.J. Am. Chem. Soc., 2012, 134 (24), pp 10244–10250 (Article) DOI: 10.1021/ja303280r
6.J. Am. Chem. Soc., 2013, 135 (28), pp 10190–10193 (Communication) DOI: 10.1021/ja4018804
7.J. Am. Chem. Soc., 2015, 137 (13), pp 4543–4549 (Article) DOI: 10.1021/jacs.5b01566
8.J. Am. Chem. Soc., 2017, 139 (21), pp 7168–7171 (Communication) DOI: 10.1021/jacs.7b03153
9.J. Am. Chem. Soc., 2019, 141 (16), pp 6583–6591 (Article) DOI: 10.1021/jacs.8b13675
10.J. Am. Chem. Soc., 2019, 141 (3), pp 1280–1289 (Article) DOI: 10.1021/jacs.8b10526
11.Angew. Chem. Int. Edit., 2003, 42(28), 3260-3263 10.1002/anie.200351128
12.Angew. Chem. Int. Edit., 2004, 43(20), 2690-2694 10.1002/anie.200352973
13.Angew. Chem. Int. Edit., 2008, 47(38), 7293-7296 10.1002/anie.200802805
14.Angew. Chem. Int. Edit., 2009, 48(36), 6675-6677 10.1002/anie.200902911
15.Angew. Chem. Int. Edit., 2011, 50(46), 10834-10838 10.1002/anie.201105375
16.Angewandte Chemie International Edition Volume 54, Issue 32, August 3, 2015, Pages: 9376–9380, DOI: 10.1002/anie.201503614
17.Angewandte Chemie International Edition Volume 55, Issue 38, September 12, 2016, Pages: 11452–11456, DOI: 10.1002/anie.201605420
18.Angewandte Chemie International Edition Volume 56, Issue 25, June 12, 2017, Pages: 7062–7065, DOI: 10.1002/anie.201612629
19.Angewandte Chemie International Edition Volume 57, Issue 38, September 17, 2018, Pages 12519-12523, 10.1002/anie.201807373
20.Angewandte Chemie International Edition Volume 57, Issue 28, July 9, 2018, Pages 8649-8653, 10.1002/anie.201804620
21.Angewandte Chemie International Edition Volume 58, Issue 31, July 29, 2019, Pages 10553-10557, 10.1002/anie.201903243
22.Angewandte Chemie International Edition Volume 58, Issue 18, April 23, 2019, Pages 6028-6032, 10.1002/anie.201901882
23.Angewandte Chemie International Edition Volume 59, Issue 42, October 12, 2020, Pages 18748-18754, 10.1002/anie.202008516
24.Angewandte Chemie International Edition Early View First published: 05 January 2021 10.1002/anie.202017001

陈弓通讯J/A (Article & Review)
1.J. Am. Chem. Soc. 2021, 143, 1195-1202. DOI: 10.1021/jacs.0c12333
2.J. Am. Chem. Soc. 2019, 141, 18230-18237. DOI: 10.1021/jacs.9b09127
3.J. Am. Chem. Soc., 2019, 141, 9401-9407. DOI: 10.1021/jacs.9b04221
4.J. Am. Chem. Soc., 2019, 141, 7194-7201. DOI: 10.1021/jacs.9b02811
5.J. Am. Chem. Soc., 2018, 140, 9678-9684. DOI:10.1021/jacs.8b05753
6.J. Am. Chem. Soc., 2018, 140, 3542-3546. DOI:10.1021/jacs.8b00641
7.J. Am. Chem. Soc. 2016, 138, 3926-3932, DOI: 10.1021/jacs.6b01384
8.J. Am. Chem. Soc. 2015, 137, 531-539. DOI: 10.1021/ja511557h
9.J. Am. Chem. Soc. 2013, 135, 12135−12141. DOI: 10.1021/ja406484v
10.J. Am. Chem. Soc. 2013, 135, 2124−2127. DOI: 10.1021/ja312277g
11.J. Am. Chem. Soc. 2012, 134, 7313−7316. DOI: 10.1021/ja3023972
12.J. Am. Chem. Soc. 2012, 134, 3−6. DOI: 10.1021/ja210660g
13.Angew. Chem., Int. Ed. 2021, Early View. DOI: 10.1002/anie.202016267
14.Angew. Chem., Int. Ed. 2016, 55, 15387-15391. DOI: 10.1002/anie.201609337
15.Angew. Chem., Int. Ed. 2013, 52, 11124−11128. DOI: 10.1002/anie.201305615
16.Angew. Chem., Int. Ed. 2011, 50, 5192−5196. DOI: 10.1002/anie.201100984
17.Angew. Chem., Int. Ed. 2010, 49, 958−961. DOI: 10.1002/anie.200905134

gdqqdl

程津培 2001年以来通讯5A+10J
1.Angewandte Chemie International Edition Volume 59, Issue 52, December 21, 2020, Pages 23782-23790, 10.1002/anie.202011313
2.Angewandte Chemie International Edition Volume 58, Issue 18, April 23, 2019, Pages 5983-5987, 10.1002/anie.201901456
3.Angewandte Chemie International Edition Volume 55, Issue 22, May 23, 2016, Pages 6506-6510, 10.1002/anie.201601028
4.Angewandte Chemie International Edition Volume 45, Issue 24, June 12, 2006, Pages 3954-3957, 10.1002/anie.200600536
5.Angewandte Chemie International Edition Volume 45, Issue 19, May 5, 2006, Pages 3093-3097, 10.1002/anie.200600048
6.Journal of the American Chemical Society  2018, 140, 28, 8611-8623 (Perspective) DOI: 10.1021/jacs.8b04104
7.Journal of the American Chemical Society  2016, 138, 17, 5523-5526 (Communication) DOI: 10.1021/jacs.6b02607
8.Journal of the American Chemical Society  2013, 135, 20, 7462-7473 (Article) DOI: 10.1021/ja309133z
9.Journal of the American Chemical Society  2010, 132, 20, 7216-7228 (Article) DOI: 10.1021/ja102819g
10.Journal of the American Chemical Society  2008, 130, 8, 2501-2516 (Article) DOI: 10.1021/ja075523m
11.Journal of the American Chemical Society  2007, 129, 11, 3074-3075 (Communication) DOI: 10.1021/ja069372j
12.Journal of the American Chemical Society  2005, 127, 8, 2696-2708 (Article) DOI: 10.1021/ja0443676
13.Journal of the American Chemical Society  2003, 125, 50, 15298-15299 (Communication) DOI: 10.1021/ja0385179
14.Journal of the American Chemical Society  2002, 124, 33, 9887-9893 (Article) DOI: 10.1021/ja0201956
15.Journal of the American Chemical Society  2001, 123, 12, 2903-2904 (Communication) DOI: 10.1021/ja000384t

16.Journal of the American Chemical Society  2000, 122, 41, 9987-9992 (Article) DOI: 10.1021/ja994120m
17.Journal of the American Chemical Society  1998, 120, 39, 10266-10267 (Communication) DOI: 10.1021/ja982086q
18.Journal of the American Chemical Society  1997, 119, 39, 9125-9129 (Article) DOI: 10.1021/ja971230p

gdqqdl

刘育24篇，是不是上榜年龄最大的，也是唯一一个高考恢复前上大学的？而且都是自己组发的，不是在校外有课题组，也不是校内趁其他课题组的通讯论文。

刚看到还有朱道本，还有程津培的15篇。

gdqqdl

周期林少了3篇
Angewandte Chemie International Edition Volume 60, Issue 6, February 8, 2021, Pages 2948-2951, 10.1002/anie.202012485
Angewandte Chemie International Edition Volume 41, Issue 13, July 3, 2002, Pages 2348-2350, 10.1002/1521-3773(20020703)41:13<2348::AID-ANIE2348>3.0.CO;2-K
Journal of the American Chemical Society  2003, 125, 15, 4404-4405 (Communication) DOI: 10.1021/ja029907i

朱守非少了1篇
Angewandte Chemie International Edition Volume 50, Issue 48, November 25, 2011, Pages 11483-11486, 10.1002/anie.201105485
https://onlinelibrary.wiley.com/doi/epdf/10.1002/anie.201105485
Asymmetric NH Insertion Reaction Cooperatively Catalyzed by Rhodium and Chiral Spiro Phosphoric Acids
Bin Xu, Shou‐Fei Zhu,* Xiu‐Lan Xie, Jun‐Jie Shen, Qi‐Lin Zhou*

刘育少了5篇
Journal of the American Chemical Society  2005, 127, 2, 657-666 (Article) DOI: 10.1021/ja046294w
Angew. Chem. Int. Edit., 2003, 42(28), 3260-3263 10.1002/anie.200351128
Angew. Chem. Int. Edit., 2004, 43(20), 2690-2694 10.1002/anie.200352973
Angewandte Chemie International Edition Volume 56, Issue 25, June 12, 2017, Pages: 7062–7065, DOI: 10.1002/anie.201612629
Angewandte Chemie International Edition Early View First published: 05 January 2021 10.1002/anie.202017001

陈军少了2篇
ANGEWANDTE CHEMIE INTERNATIONAL EDITION Volume 56, Issue 21, May 15, 2017, Pages: 5785–5789, DOI: 10.1002/anie.201701928
ANGEWANDTE CHEMIE INTERNATIONAL EDITION Volume 56, Issue 41, October 2, 2017, Pages: 12561–12565, DOI: 10.1002/anie.201706604

几篇重复
10.1002/ange.201912182=10.1002/anie.201912182
10.1002/ange.202002724=10.1002/anie.202002724
10.1002/ange.201916534=10.1002/anie.201916534
10.1002/ange.201915992=10.1002/anie.201915992
10.1002/ange.201910743=10.1002/anie.201910743

gdqqdl

游书力少了18篇
1.Journal of the American Chemical Society  2010, 132, 33, 11418-11419 (Communication) DOI: 10.1021/ja105111n
2.Journal of the American Chemical Society  2010, 132, 12, 4056-4057 (Communication) DOI: 10.1021/ja100207s
3.Journal of the American Chemical Society  2009, 131, 24, 8346-8347 (Communication) DOI: 10.1021/ja901384j
4.Journal of the American Chemical Society  2007, 129, 6, 1484-1485 (Communication) DOI: 10.1021/ja067417a
5.Angew. Chem. Int. Ed. 2019, 58, 18069-18074. 10.1002/anie.201911144
6.Angew. Chem. Int. Ed. 2017, 56, 7252-7256. 10.1002/anie.201703674
7.Angew. Chem. Int. Ed. 2017, 56, 7440-7443. 10.1002/anie.201703178
8.Angew. Chem. Int. Ed. 2017, 56, 10545-10548. 10.1002/anie.201705068
9.Angew. Chem. Int. Ed. 2017, 56, 4540-4544. 10.1002/anie.201700021
10.Angew. Chem. Int. Ed. 2014, 53, 2443-2446. 10.1002/anie.201309081
11.Angew. Chem. Int. Ed. 2012, 51, 12662-12686. 10.1002/anie.201204822
12.Angew. Chem. Int. Ed. 2012, 51, 1680-1683. 10.1002/anie.201107677
13.Angew. Chem. Int. Ed. 2011, 50, 8665-8669. 10.1002/anie.201103937
14.Angew. Chem. Int. Ed. 2011, 50, 4455-4458. 10.1002/anie.201100206
15.Angew. Chem. Int. Ed. 2010, 49, 8666-8669. 10.1002/anie.201003919
16.Angew. Chem. Int. Ed. 2010, 49, 1496-1499. 10.1002/anie.200906638
17.Angew. Chem. Int. Ed. 2009, 48, 7428-7431. 10.1002/anie.200903462
18.Angew. Chem. Int. Ed. 2006, 45, 5246-5248. 10.1002/anie.200601889
Angew. Chem. Int. Ed. 2010, 49, 5826-5828. 10.1002/anie.201000799 (Highlights)

2021还有3篇在线接收
Angewandte Chemie International Edition Accepted Articles First published: 25 January 2021 10.1002/anie.202013174
Angewandte Chemie International Edition Early View First published: 15 January 2021 10.1002/anie.202016899
Journal of the American Chemical Society  2021, 143, 1, 114-120 (Communication) DOI: 10.1021/jacs.0c11735