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Twin research and human genetics : the official journal of the International Society for Twin Studies, ISSN 1832-4274, 04/2017, Volume 20, Issue 2, pp. 186 - 186
The publishers regret to announce that the affiliation for the above paper was incorrectly inserted. The correct affiliation is below: Aniket Mishra1, Genetics... 
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2018, Volume 360, Issue 12, pp. 2291 - 2296
Rhodium catalyzed synthesis of chalcogenated N ‐aryl‐7‐azaindoles/azaindolines has been developed through N‐directed ortho C sp 2 −H activation in presence of... 
7-azaindoles | sulfur | C−H bond activation | 7-azaindolines | selenium | rhodium | C(SP)-H BONDS | ROOM-TEMPERATURE | ARENES | C-H bond activation | CHEMISTRY, ORGANIC | BOND FORMATION | ANTITUMOR-ACTIVITY | DIRECT THIOLATION | ALIPHATIC AMIDES | EFFICIENT ACCESS | SULFURATING REAGENT | CHEMISTRY, APPLIED | Sulfur compounds | Dioxane | Carbonates | Rhodium | Chemical synthesis | Aromatic compounds | Substrates | Molecular chains | Biological materials
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 09/2018, Volume 360, Issue 17, pp. 3228 - 3232
A cobalt‐catalyzed sp 2 C−H acetoxylation of amides having 8‐aminoquinoline as a directing group has been achieved using manganese(III) acetate both as an... 
manganese(III) acetate | C−H bond activation | acetoxylation | Cobalt | 8-aminoquinoline | Amides | Aromatic compounds | Functional groups | Manganese
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 07/2016, Volume 358, Issue 14, pp. 2267 - 2272
Imino‐/enaminophosphonates derived from amines and diethyl phenacyl phosphonates undergo oxidative cyclization via CH bond activation catalyzed by palladium... 
ketophosphonates | indoles | imine‐enamines | CH bond activation | phosphonates | pyrroles | imine-enamines | N-ARYL ENAMINES | PHOSPHORYLATION | ANNULATION | ARYLATION | C-H bond activation | CHEMISTRY, ORGANIC | BOND FORMATION | INDOLE-DERIVATIVES | C-H ACTIVATION | FUNCTIONALIZATION | AMINATION | INHIBITORS | CHEMISTRY, APPLIED | Palladium | Phosphonates | Synthesis | Amines | Chlorides | Activation | Catalysis | Bonding
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 08/2016, Volume 81, Issue 15, pp. 6525 - 6534
An efficient, highly regioselective, and scalable ruthenium-catalyzed o-aryl C-H mono-cyanation of N-aryl-7azaindoles to form N-(2-cyanoaryl)-7-azaindoles has... 
BORONIC ACIDS | PALLADIUM | ELECTROPHILIC CYANATION | NATURAL-PRODUCTS | ARYL HALIDES | EFFICIENT SYNTHESIS | CYANO SOURCE | CHEMISTRY, ORGANIC | 7-AZAINDOLES | INDOLES | PHENYL-P-TOLUENESULFONAMIDE
Journal Article
by Malik, Rainer and Chauhan, Ganesh and Traylor, Matthew and Sargurupremraj, Muralidharan and Okada, Yukinori and Mishra, Aniket and Rutten-Jacobs, Loes and Giese, Anne-Katrin and Van Der Laan, Sander W and Gretarsdottir, Solveig and Anderson, Christopher D and Chong, Michael and Adams, Hieab H. H and Ago, Tetsuro and Almgren, Peter and Amouyel, Philippe and Ay, Hakan and Bartz, Traci M and Benavente, Oscar R and Bevan, Steve and Boncoraglio, Giorgio B and Brown, Robert D and Butterworth, Adam S and Carrera, Caty and Carty, Cara L and Chasman, Daniel I and Chen, Wei-Min and Cole, John W and Correa, Adolfo and Cotlarciuc, Ioana and Cruchaga, Carlos and Danesh, John and De Bakker, Paul I. W and Destefano, Anita L and Den Hoed, Marcel and Duan, Qing and Engelter, Stefan T and Falcone, Guido J and Gottesman, Rebecca F and Grewal, Raji P and Gudnason, Vilmundur and Gustafsson, Stefan and Haessler, Jeffrey and Harris, Tamara B and Hassan, Ahamad and Havulinna, Aki S and Heckbert, Susan R and Holliday, Elizabeth G and Howard, George and Hsu, Fang-Chi and Hyacinth, Hyacinth I and Ikram, M. Arfan and Ingelsson, Erik and Irvin, Marguerite R and Jian, Xueqiu and Jiménez-Conde, Jordi and Johnson, Julie A and Jukema, J. Wouter and Kanai, Masahiro and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Kooperberg, Charles and Kubo, Michiaki and Lange, Leslie A and Langefeld, Carl D and Langenberg, Claudia and Launer, Lenore J and Lee, Jin-Moo and Lemmens, Robin and Leys, Didier and Lewis, Cathryn M and Lin, Wei-Yu and Lindgren, Arne G and Lorentzen, Erik and Magnusson, Patrik K and Maguire, Jane and Manichaikul, Ani and McArdle, Patrick F and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Ninomiya, Toshiharu and O'Donnell, Martin J and Psaty, Bruce M and Pulit, Sara L and Rannikmäe, Kristiina and Reiner, Alexander P and Rexrode, Kathryn M and Rice, Kenneth and Rich, Stephen S and Ridker, Paul M and Rost, Natalia S and Rothwell, Peter M and Rotter, Jerome I and Rundek, Tatjana and Sacco, Ralph L and Sakaue, Saori and Sale, Michele M and ... and AFGen Consortium and UK Young Lacunar DNA Study and EPIC-CVD Consortium and Int Stroke Genetics Consortium ISG and INVENT Consortium and Int Genomics Blood Pressure iGEN and MEGASTROKE Consortium and COMPASS Consortium and METASTROKE Consortium and EPIC-InterAct Consortium and Cohorts Heart Aging Res Genomic and BioBank Japan Cooperative Hosp Grp and NINDS Stroke Genetics Network Si and STARNET and Neurology Working Grp Charge Con and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and International Genomics of Blood Pressure (iGEN-BP) Consortium and BioBank Japan Cooperative Hospital Group and Neurology Working Group of the CHARGE Consortium and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 524 - 537
Journal Article
by Verhoeven, Virginie J. M and Hysi, Pirro G and Wojciechowski, Robert and Fan, Qiao and Guggenheim, Jeremy A and Höhn, René and Macgregor, Stuart and Hewitt, Alex W and Nag, Abhishek and Cheng, Ching-Yu and Yonova-Doing, Ekaterina and Zhou, Xin and Ikram, M. Kamran and Buitendijk, Gabriëlle H. S and McMahon, George and Kemp, John P and Pourcain, Beate St and Simpson, Claire L and Mäkelä, Kari-Matti and Lehtimäki, Terho and Kähönen, Mika and Paterson, Anew D and Hosseini, S. Mohsen and Wong, Hoi Suen and Xu, Liang and Jonas, Jost B and Pärssinen, Olavi and Wedenoja, Juho and Yip, Shea Ping and Ho, Daniel W. H and Pang, Chi Pui and Chen, Li Jia and Burdon, Kathryn P and Craig, Jamie E and Klein, Barbara E. K and Klein, Ronald and Haller, Toomas and Metspalu, Anes and Khor, Chiea-Chuen and Tai, E.-Shyong and Aung, Tin and Vithana, Eranga and Tay, Wan-Ting and Barathi, Veluchamy A and Chen, Peng and Li, Ruoying and Liao, Jiemin and Zheng, Yingfeng and Ong, Rick T and Döring, Angela and Evans, David M and Timpson, Nicholas J and Verkerk, Annemieke J. M. H and Meitinger, Thomas and Raitakari, Olli and Hawthorne, Felicia and Spector, Tim D and Karssen, Lennart C and Pirastu, Mario and Murgia, Federico and Ang, Wei and Mishra, Aniket and Montgomery, Grant W and Pennell, Craig E and Cumberland, Phillippa M and Cotlarciuc, Ioana and Mitchell, Paul and Wang, Jie Jin and Schache, Maria and Janmahasathian, Sarayut and Igo, Robert P and Lass, Jonathan H and Chew, Emily and Iyengar, Sudha K and Gorgels, Theo G. M. F and Rudan, Igor and Hayward, Caroline and Wright, Alan F and Polasek, Ozren and Vatavuk, Zoran and Wilson, James F and Fleck, Brian and Zeller, Tanja and Mirshahi, Alireza and Müller, Christian and Uitterlinden, Ané G and Rivadeneira, Fernando and Vingerling, Johannes R and Hofman, Albert and Oostra, Ben A and Amin, Najaf and Bergen, Arthur A. B and teo, Yik-Ying and Rahi, Jugnoo S and Vitart, Veronique and Williams, Cathy and Baird, Paul N and Wong, Tien-Yin and Oexle, Konrad and Pfeiffer, Norbert and ... and Fuchs' Genetics Multi-Ctr Study Gr and Diabet Control Complications Trial and WTCCC2 and CREAM and Consortium for Refractive Error and Myopia (CREAM) and Fuchs' Genetics Multi-Center Study Group and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and Wellcome Trust Case Control Consortium 2 (WTCCC2) and The Fuchs' Genetics Multi-Center Study Group and The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 3, pp. 314 - 318
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 12/2017, Volume 82, Issue 23, pp. 12406 - 12415
A silver- and copper-free rhodium-catalyzed C-H acetoxylation reaction of azaindoles has been achieved at near ambient temperature employing PIDA as a... 
Anhydrides | Rhodium | Hydrogen | Analysis | Indole | Chemical properties | Chemical synthesis | Electric properties
Journal Article
Materials Science and Engineering. A, Structural Materials: Properties, Microstructure and Processing, ISSN 0921-5093, 10/2016, Volume 676, Issue C
Journal Article
Advanced Synthesis and Catalysis, ISSN 1615-4150, 09/2018, Volume 360, Issue 17, pp. 3228 - 3232
Journal Article
Asian Journal of Organic Chemistry, ISSN 2193-5807, 06/2019, Volume 8, Issue 6, pp. 819 - 822
Direct thiolation of quinazolinones by selective cleavage of a relatively inert C−H bond, mediated by earth‐abundant copper and guided by a pyridine or... 
copper | C−H activation | thioquinazolinones | thiopyrimidinone | thiolation | C(SP)-H BONDS | ARENES | CHEMISTRY, ORGANIC | SULFENYLATION | CYANATION | CATALYZED DIRECT THIOLATION | CHALCOGENATION | C-H activation | ANTIINFLAMMATORY AGENTS | BIOLOGICAL EVALUATION | DERIVATIVES | SP | Quinazolinones | Hydrogen bonds | Copper | Reagents
Journal Article