doi;authors;title;year;journal;affiliations;citations_year_avg;origin_count;origin;citations_avg
10.1038/nature14885;"Jin J.; MacMillan D.W.C.";Alcohols as alkylating agents in heteroarene C-H functionalization;2015;Nature;Merck Center for Catalysis, Princeton University, Princeton, 08544, NJ, United States;61;1;sci;550
10.1002/anie.202002900;"Lai X.-L.; Shu X.-M.; Song J.; Xu H.-C.";Electrophotocatalytic Decarboxylative C?H Functionalization of Heteroarenes;2020;Angewandte Chemie - International Edition;"State Key Laboratory of Physical Chemistry of Solid Surfaces, Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China; College of Chemistry and Institute of Green Catalysi";36;1;sci;143
10.1039/c6sc02653b;"Li G.-X.; Morales-Rivera C.A.; Wang Y.; Gao F.; He G.; Liu P.; Chen G.";Photoredox-mediated Minisci C-H alkylation of N-heteroarenes using boronic acids and hypervalent iodine;2016;Chemical Science;"State Key Laboratory and Institute of Elemento-Organic Chemistry, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin, 300071, China; Department of Chemistry, University of Pittsburgh, Pittsburgh, 152";31;3;sci, sco, wos;248
10.1039/c7sc00283a;"Matsui J.K.; Primer D.N.; Molander G.A.";Metal-free C-H alkylation of heteroarenes with alkyltrifluoroborates: A general protocol for 1ř, 2ř and 3ř alkylation;2017;Chemical Science;Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, 19104-6323, PA, United States;31;1;sco;218
10.1021/jacs.2c02062;"Sakai H.A.; Macmillan D.W.C.";Nontraditional Fragment Couplings of Alcohols and Carboxylic Acids: C(sp3)-C(sp3) Cross-Coupling via Radical Sorting;2022;Journal Of The American Chemical Society;Merck Center for Catalysis at Princeton University, Princeton, 08544, NJ, United States;30;1;sci;60
10.1021/jacs.7b05899;"Guti‚rrez-Bonet µ.; Remeur C.; Matsui J.K.; Molander G.A.";Late-Stage C-H Alkylation of Heterocycles and 1,4-Quinones via Oxidative Homolysis of 1,4-Dihydropyridines;2017;Journal Of The American Chemical Society;Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, 19104-6323, PA, United States;28;1;sci;197
10.1021/acscatal.9b04411;"Wang Z.; Liu Q.; Ji X.; Deng G.-J.; Huang H.";Bromide-promoted visible-light-induced reductive minisci reaction with aldehydes;2020;Acs Catalysis;Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan, 411105, China;24;2;sci, sco;97
10.1021/acs.accounts.2c00607;"Beil S.B.; Chen T.Q.; Intermaggio N.E.; Macmillan D.W.C.";Carboxylic Acids as Adaptive Functional Groups in Metallaphotoredox Catalysis;2022;Accounts Of Chemical Research;Merck Center for Catalysis at Princeton University, Princeton, 8544, NJ, United States;24;1;sci;48
10.1021/jacs.0c04499;"Jung S.; Shin S.; Park S.; Hong S.";Visible-Light-Driven C4-Selective Alkylation of Pyridinium Derivatives with Alkyl Bromides;2020;Journal Of The American Chemical Society;"Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, South Korea; Center for Catalytic Hydrocarbon Functionalizations, Institute for Basic Science (IBS), Daejeon, 34141, South Korea";22;1;sci;89
10.1002/anie.201707958;"Nuhant P.; Oderinde M.S.; Genovino J.; Juneau A.; Gagn‚ Y.; Allais C.; Chinigo G.M.; Choi C.; Sach N.W.; Bernier L.; Fobian Y.M.; Bundesmann M.W.; Khunte B.; Frenette M.; Fadeyi O.O.";Visible-Light-Initiated Manganese Catalysis for C?H Alkylation of Heteroarenes: Applications and Mechanistic Studies;2017;Angewandte Chemie - International Edition;"Pfizer Medicine Design & Oncology Medicinal Chemistry, 445 Eastern Point Road, Groton, 06340, CT, United States; Department de Chimie, Universit‚ du Qu‚bec   Montr‚al, Case Postale 8888, Succursale Centre-Ville, Montr‚al, H3C 3P8, QC, Canada";21;1;sco;144
10.1039/c8sc04892d;"Dong J.; Lyu X.; Wang Z.; Wang X.; Song H.; Liu Y.; Wang Q.";Visible-light-mediated Minisci C-H alkylation of heteroarenes with unactivated alkyl halides using O2 as an oxidant;2019;Chemical Science;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin,";19;3;sci, sco, wos;95
10.1039/d0cc05391k;"Niu K.; Song L.; Hao Y.; Liu Y.; Wang Q.";Electrochemical decarboxylative C3 alkylation of quinoxalin-2(1: H)-ones with N -hydroxyphthalimide esters;2020;Chemical Communications;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin,";18;1;sci;73
10.1002/anie.201603329;"Jo W.; Kim J.; Choi S.; Cho S.H.";Transition-Metal-Free Regioselective Alkylation of Pyridine N-Oxides Using 1,1-Diborylalkanes as Alkylating Reagents;2016;Angewandte Chemie - International Edition;Department of Chemistry and Division of Advanced Nuclear Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 790-784, South Korea;17;1;sci;137
10.1021/jacs.1c05890;"Qi R.; Wang C.; Huo Y.; Chai H.; Wang H.; Ma Z.; Liu L.; Wang R.; Xu Z.";Visible Light Induced Cu-Catalyzed Asymmetric C(sp3)-H Alkylation;2021;Journal Of The American Chemical Society;"School of Basic Medical Science, Lanzhou University, Lanzhou, 730000, China; School of Pharmacy, Lanzhou University, Lanzhou, 730000, China; Research Unit of Peptide Science, Chinese Academy of Medical Sciences, 2019RU066, Lanzhou, 730000, China";17;1;sci;51
10.1021/acs.orglett.8b01085;"Genovino J.; Lian Y.; Zhang Y.; Hope T.O.; Juneau A.; Gagn‚ Y.; Ingle G.; Frenette M.";Metal-Free-Visible Light C-H Alkylation of Heteroaromatics via Hypervalent Iodine-Promoted Decarboxylation;2018;Organic Letters;"Pfizer Worldwide Medicinal Chemistry, Eastern Point Road, Groton, 06340, CT, United States; D‚partement de Chimie, Universit‚ du Qu‚bec · Montr‚al, Case Postale 8888, Succursale Centre-Ville, Montr‚al, H3C 3P8, QC, Canada";16;1;sci;94
10.1039/c9gc03008e;"Wang Z.; Ji X.; Zhao J.; Huang H.";Visible-light-mediated photoredox decarbonylative Minisci-type alkylation with aldehydes under ambient air conditions;2019;Green Chemistry;"Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application, Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan, 411105, China; School of Pharm";15;3;sci, sco, wos;74
10.1002/anie.201915837;"Liu J.; Wu S.; Yu J.; Lu C.; Wu Z.; Wu X.; Xue X.-S.; Zhu C.";Polarity Umpolung Strategy for the Radical Alkylation of Alkenes;2020;Angewandte Chemie - International Edition;"Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, 199 Ren-Ai Road, Suzhou, 215123, Jiangsu, China; State Key Laboratory of Elemento-organic Chemistry, College of";15;1;sci;58
10.1021/jacs.2c00962;"Liu Z.; He J.-H.; Zhang M.; Shi Z.-J.; Tang H.; Zhou X.-Y.; Tian J.-J.; Wang X.-C.";Borane-Catalyzed C3-Alkylation of Pyridines with Imines, Aldehydes, or Ketones as Electrophiles;2022;Journal Of The American Chemical Society;State Key Laboratory and Institute of Elemento-Organic Chemistry, Haihe Laboratory of Sustainable Chemical Transformations, Frontiers Science Center for New Organic Matter, Tianjin, 300071, China;15;1;sci;30
10.1021/acs.orglett.8b02988;"Sutherland D.R.; Veguillas M.; Oates C.L.; Lee A.-L.";Metal-, Photocatalyst-, and Light-Free, Late-Stage C-H Alkylation of Heteroarenes and 1,4-Quinones Using Carboxylic Acids;2018;Organic Letters;Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, EH14 4AS, United Kingdom;14;2;sci, wos;87
10.1021/jacs.1c05278;"Choi J.; Laudadio G.; Godineau E.; Baran P.S.";Practical and Regioselective Synthesis of C-4-Alkylated Pyridines;2021;Journal Of The American Chemical Society;"Department of Chemistry, Scripps Research, 10550 North Torrey Pines Road, San Diego, 92037, CA, United States; Process Research, Syngenta Crop Protection, Schaffhauserstrasse 101, Stein, CH-4332, Switzerland";13;3;sci, sco, wos;38
10.1055/s-0037-1611658;"Sun A.C.; McAtee R.C.; McClain E.J.; Stephenson C.R.J.";Advancements in Visible-Light-Enabled Radical C(sp)                          2                          -H Alkylation of (Hetero)arenes;2019;Synthesis (Germany);Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, 48109, MI, United States;13;1;sco;67
10.1002/adsc.201500268;"Tang R.-J.; Kang L.; Yang L.";Metal-Free Oxidative Decarbonylative Coupling of Aliphatic Aldehydes with Azaarenes: Successful Minisci-Type Alkylation of Various Heterocycles;2015;Advanced Synthesis And Catalysis;College of Chemistry, Xiangtan University, Xiangtan, Hunan, 411105, China;12;3;sci, sco, wos;107
10.1021/acs.joc.1c02125;"Xu J.; Cai H.; Shen J.; Shen C.; Wu J.; Zhang P.; Liu X.";Photo-Induced Cross-Dehydrogenative Alkylation of Heteroarenes with Alkanes under Aerobic Conditions;2021;Journal Of Organic Chemistry;"Department of Chemistry, National University of Singapore, Singapore, 117543, Singapore; Center for Functional Materials, National University of Singapore Suzhou Research Institute, Suzhou, 215123, China; College of Material Chemistry and Chemical Engine";11;3;sci, sco, wos;32
10.1002/anie.202113658;"Vellakkaran M.; Kim T.; Hong S.";Visible-Light-Induced C4-Selective Functionalization of Pyridinium Salts with Cyclopropanols;2022;Angewandte Chemie - International Edition;"Center for Catalytic Hydrocarbon Functionalizations, Institute for Basic Science (IBS), South Korea; Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, South Korea";10;1;sci;19
10.1002/asia.202100151;"Parida S.K.; Hota S.K.; Kumar R.; Murarka S.";Late-Stage Alkylation of Heterocycles Using N-(Acyloxy)phthalimides;2021;Chemistry - An Asian Journal;Department of Chemistry, Indian Institute of Technology Jodhpur, Karwar, 342037, Rajasthan, India;9;1;sci;28
10.1002/ajoc.201800197;"Wang J.; Li G.-X.; He G.; Chen G.";Photoredox-Mediated Minisci Alkylation of N-Heteroarenes using Carboxylic Acids and Hypervalent Iodine;2018;Asian Journal Of Organic Chemistry;"State Key Laboratory and Institute of Elemento-Organic Chemistry, College of chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin, 300071, China";8;3;sci, sco, wos;48
10.1039/d0gc02111c;"Dong J.; Yue F.; Xu W.; Song H.; Liu Y.; Wang Q.";Visible-light-mediated minisci C-H alkylation of heteroarenes with 4-alkyl-1,4-dihydropyridines using O2as an oxidant;2020;Green Chemistry;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin,";8;3;sci, sco, wos;32
10.1002/ejoc.201900786;"Zidan M.; Morris A.O.; McCallum T.; Barriault L.";The Alkylation and Reduction of Heteroarenes with Alcohols Using Photoredox Catalyzed Hydrogen Atom Transfer via Chlorine Atom Generation;2020;European Journal Of Organic Chemistry;Centre for Catalysis, Research and Innovation, Department of Chemistry and Biomolecular Sciences, University of Ottawa, 10 Marie Curie, Ottawa, K1N 6N5, ON, Canada;8;2;sci, sco;30
10.1039/d2cc04947c;"Mondal P.P.; Pal A.; Prakash A.K.; Sahoo B.";Ketone-derived 2,3-dihydroquinazolinones in N-heteroarene C-H alkylation via C-C bond scission under oxidative metal catalysis;2022;Chemical Communications;Indian Institute of Science Education and Research (IISER) Thiruvananthapuram, Kerala, Thiruvananthapuram, 695551, India;6;1;sci;12
10.1002/ejoc.201900611;"Perkins J.J.; Schubert J.W.; Streckfuss E.C.; Balsells J.; ElMarrouni A.";Photoredox Catalysis for Silyl-Mediated C-H Alkylation of Heterocycles with Non-Activated Alkyl Bromides;2020;European Journal Of Organic Chemistry;"Department of Discovery Chemistry, MRL, Merck & Co., Inc., 770 Sumneytown Pike, West Point, Pennsylvania, 19486, PA, United States; Janssen Research & Development LLC, Pennsylvania, 19477, PA, United States";5;1;sco;20
10.1016/j.cclet.2021.03.011;"Wang J.; Liu X.; Wu Z.; Li F.; Qin T.; Zhang S.; Kong W.; Liu L.";Silver-catalyzed decarboxylative C-H functionalization of cyclic aldimines with aliphatic carboxylic acids;2021;Chinese Chemical Letters;"Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu, 476000, China; College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nanyang, 473";5;1;sci;14
10.1021/acs.orglett.9b02365;"Ghosh P.; Kwon N.Y.; Han S.; Kim S.; Han S.H.; Mishra N.K.; Jung Y.H.; Chung S.J.; Kim I.S.";Site-Selective C-H Alkylation of Diazine N-Oxides Enabled by Phosphonium Ylides;2019;Organic Letters;School of Pharmacy, Sungkyunkwan University, Suwon, 16419, South Korea;5;1;sci;24
10.1039/d1qo01223a;"Liu X.-L.; Jiang L.-B.; Luo M.-P.; Ren Z.; Wang S.-G.";Recent advances in catalytic enantioselective direct C-H bond functionalization of electron-deficient N-containing heteroarenes;2022;Organic Chemistry Frontiers;"Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Xueyuan Avenue, Shenzhen, 1068, China; College of Pharmacy, Shenzhen Technology University, Lantian Road, Shenzhen, 3002, China; School of Medical Imaging, Xuzhou Medical University";5;1;sco;14
10.1039/d1gc04479f;"He J.-Y.; Qian W.-F.; Wang Y.-Z.; Yao C.; Wang N.; Liu H.; Zhong B.; Zhu C.; Xu H.";Sustainable electrochemical dehydrogenative C(sp3)-H mono/di-alkylations;2022;Green Chemistry;Key Laboratory of Pesticides & Chemical Biology Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, 430079, China;4;1;sci;8
10.1039/d2sc05521j;"Yue F.; Ma H.; Song H.; Liu Y.; Dong J.; Wang Q.";Alkylboronic acids as alkylating agents: photoredox-catalyzed alkylation reactions assisted by K3PO4;2022;Chemical Science;State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin, 300071, China;4;1;sci;9
10.1002/anie.202109271;"Fricke P.J.; Dolewski R.D.; McNally A.";Four-Selective Pyridine Alkylation via Wittig Olefination of Dearomatized Pyridylphosphonium Ylides;2021;Angewandte Chemie - International Edition;Department of Chemistry, Colorado State University, Fort Collins, 80523, CO, United States;3;3;sci, sco, wos;9
10.1021/acs.joc.9b02848;"Wang Z.; Dong J.; Hao Y.; Li Y.; Liu Y.; Song H.; Wang Q.";Photoredox-Mediated Minisci C-H Alkylation Reactions between N-Heteroarenes and Alkyl Iodides with Peroxyacetate as a Radical Relay Initiator;2019;Journal Of Organic Chemistry;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin,";3;3;sci, sco, wos;14
10.1039/c9qo00690g;"Dong J.; Wang X.; Wang Z.; Song H.; Liu Y.; Wang Q.";Metal-, photocatalyst-, and light-free late-stage C-H alkylation of N-heteroarenes with organotrimethylsilanes using persulfate as a stoichiometric oxidant;2019;Organic Chemistry Frontiers;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin, 300071, China";3;2;sci, sco;13
10.1038/s44160-022-00125-1;"Cao H.; Kong D.; Yang L.-C.; Chanmungkalakul S.; Liu T.; Piper J.L.; Peng Z.; Gao L.; Liu X.; Hong X.; Wu J.";Br›nsted acid-enhanced direct hydrogen atom transfer photocatalysis for selective functionalization of unactivated C(sp 3)-H bonds;2022;Nature Synthesis;"Department of Chemistry, National University of Singapore, Singapore, Singapore; National University of Singapore (Suzhou) Research Institute, Suzhou, China; School of Chemical Engineering & Technology, Harbin Institute of Technology, Harbin, China; Cent";3;1;sci;7
10.1039/c9cc08056b;"Tian H.; Xu W.; Liu Y.; Wang Q.";Radical alkylation of C(sp3)-H bonds with diacyl peroxides under catalyst-free conditions;2019;Chemical Communications;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin, 300071, China";3;1;sci;16
10.1021/acs.joc.9b00972;"Dong J.; Wang Z.; Wang X.; Song H.; Liu Y.; Wang Q.";Metal-, Photocatalyst-, and Light-Free Minisci C-H Alkylation of N-Heteroarenes with Oxalates;2019;Journal Of Organic Chemistry;"State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin,";2;3;sci, sco, wos;10
10.1021/acs.orglett.2c03206;"Mooney D.T.; Moore P.R.; Lee A.-L.";Direct Minisci-Type C-H Amidation of Purine Bases;2022;Organic Letters;"Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, EH14 4AS, United Kingdom; Early Chemical Development, Pharmaceutical Sciences, R&D BioPharmaceuticals, AstraZeneca, Macclesfield, SK10 2NA, United Kingdom";2;2;sci, sco;3
10.1002/adsc.201501009;"Khan R.; Felix R.; Kemmitt P.D.; Coles S.J.; Day I.J.; Tizzard G.J.; Spencer J.";"Late Stage C-H Activation of a Privileged Scaffold; Synthesis of a Library of Benzodiazepines";2016;Advanced Synthesis And Catalysis;"Department of Chemistry, School of Life Sciences, University of Sussex, Falmer, BN1 9QJ, United Kingdom; Tocris Bioscience, Tocris House, IO Centre, Moorend Farm Avenue, Bristol, BS11 0QL, United Kingdom; AstraZeneca, Mereside Alderley Park, Macclesfield";2;1;sci;16
10.1002/asia.201800534;"Ge L.; Jian W.; Zhou H.; Chen S.; Ye C.; Yu F.; Qian B.; Li Y.; Bao H.";Iron-Catalyzed Vinylic C?H Alkylation with Alkyl Peroxides;2018;Chemistry - An Asian Journal;Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, State Key Laboratory of Structural Chemistry, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, University of Chinese Academy of Sc;2;1;sci;10
10.1039/c7ob01083d;"Lei B.; Wang X.; Ma L.; Jiao H.; Zhu L.; Li Z.";DDQ-promoted direct C5-alkylation of oxazoles with alkylboronic acids: Via palladium-catalysed C-H bond activation;2017;Organic And Biomolecular Chemistry;Department of Pharmaceutical and Biological Engineering, School of Chemical Engineering, Sichuan University, Chengdu, 610065, China;2;1;sci;14
10.1039/d1ob01806j;"Yue F.; Dong J.; Liu Y.; Wang Q.";Visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones;2021;Organic And Biomolecular Chemistry;State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin, 300071, China;2;1;sci;6
10.1055/a-1294-0158;"Chen X.; Luo X.; Wang K.; Liang F.; Wang P.";Late-Stage Alkylation of N-Containing Heteroarenes Enabled by Homolysis of Alkyl-1,4-dihydropyridines under Blue LED Irradiation;2021;Synlett;"Key Lab. of Optoelectron. Devices and Syst. of Min. of Educ. and Guangdong Prov. and Coll. of Phys. and Optoelectron. Eng., Shenzhen University, Shenzhen, 518060, China; Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemist";2;1;sci;6
10.1002/chem.202203332;"Tang L.; Lv G.; Cheng R.; Yang F.; Zhou Q.";Three-Component Perfluoroalkylvinylation of Alkenes Enabled by Dual DBU/Fe Catalysis**;2023;Chemistry - A European Journal;"College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang, 464000, China; Key Laboratory of Utilization of Non-metallic Mineral in the South of Henan, Xinyang, 464000, China";1;1;sci;2
10.1038/s42004-023-00947-w;"Kang H.; Tan L.; Han J.-T.; Huang C.-Y.; Su H.; Kavun A.; Li C.-J.";Acceptorless cross-dehydrogenative coupling for C(sp3)-H heteroarylation mediated by a heterogeneous GaN/ketone photocatalyst/photosensitizer system;2023;Communications Chemistry;Department of Chemistry, FRQNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke Street W., Montr‚al, H3A0B8, QC, Canada;1;1;sco;1
10.1021/acs.joc.3c01625;"Rosadoni E.; Bombonato E.; Del Vecchio A.; Guariento S.; Ronchi P.; Bellina F.";Direct Decarboxylative C-2 Alkylation of Azoles through Minisci-Type Coupling;2023;Journal Of Organic Chemistry;"Department of Chemistry and Industrial Chemistry, University of Pisa, Via Moruzzi 13, Pisa, 56124, Italy; Chemistry Research and Drug Design, Chiesi Farmaceutici S.p.A., Largo Belloli 11/A, Parma, 43122, Italy; Department of Chemistry ""Giacomo Ciamician""";0;3;sci, sco, wos;0
10.1002/ejoc.202201491;"Liu G.; Mu X.; Tian M.; Wang W.; Zou C.; Chen Y.; Yu M.";Metal-Free, Light-Mediated, Site-Specific, Radical C6?H Alkylation of Purines with Alcohols Intervened by Oxalates without Catalysts;2023;European Journal Of Organic Chemistry;"School of Chemistry and Materials Science, Ludong University, Shandong Province, Yantai, 264025, China; College of Chemistry and Chemical Engineering, Yantai University, Shandong Province, Yantai, 264025, China";0;1;sci;0
10.1002/jhet.4659;"Liu X.; Sun X.; Wang W.; Tian M.; Chen Y.; Zou C.; Yu M.";Light, metal-free regioselective C6-H alkylation of purines and purine nucleosides with alcohols;2023;Journal Of Heterocyclic Chemistry;"School of Chemistry and Materials Science, Ludong University, Yantai, China; College of Chemistry and Chemical Engineering, Yantai University Yantai, Yantai, China";0;1;sci;0
10.1007/978-981-10-3421-3_8;"Fujiwara Y.; Baran P.S.";Radical-based late stage c-h functionalization of heteroaromatics in drug discovery;2017;New Horizons Of Process Chemistry: Scalable Reactions And Technologies;"Department of Medicinal Chemistry, Meiji Seika Pharma Co., Ltd, 760 Morooka-Cho, Yokohama-shi, 222-8567, Kanagawa, Japan; Department of Chemistry and Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Rd, La Jolla, 92037, CA, Unit";0;1;sci;2
10.1016/b978-0-12-818349-6.00002-9;"Capurro P.; Basso A.";Chemical reactions for building small molecules;2019;Small Molecule Drug Discovery: Methods, Molecules And Applications;Department of Chemistry and Industrial Chemistry, University of Genova, Genova, Italy;0;1;sci;1
10.1016/j.tetlet.2022.153846;"Li L.; Song X.; Qi M.-F.; Sun B.";Weak Br›nsted base-promoted photoredox catalysis for C-H alkylation of heteroarenes mediated by triplet excited diaryl ketone;2022;Tetrahedron Letters;"School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China; China Tobacco Hubei Industrial L.L.C., Wuhan, 430030, China";0;1;sci;1
10.1021/acs.orglett.3c03469;"Xu L.-C.; Ma X.-D.; Liu K.-M.; Duan X.-F.";Chemo- and Regioselective Alkylation of Pyridine N-Oxides with Titanacyclopropanes;2023;Organic Letters;College of Chemistry, Beijing Normal University, Beijing, 100875, China;0;1;sci;0
10.1055/s-1294-0158;"Chen X.; Luo X.; Wang K.; Liang F.; Wang P.";Late-stage alkylation of N-containing heteroarenes enabled by homolysis of alkyl-1,4-dihydropyridines under blue LED irradiation;2020;Synlett;"Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering Shenzhen University, Shenzhen, 518060, China; Shanghai Key Laboratory for Molecular Engineering of Chi";0;1;sci;0
10.14233/ajchem.2019.21635;"Khalid M.; Mohammed S.";Recent free-radical reactions;2019;Asian Journal Of Chemistry;Department of Chemistry, Faculty of Science, Zakho University, Kurdistan, Zakho, Iraq;0;1;sci;2