| Year |
Citation |
Score |
| 2024 |
Lee YT, Chan CY, Matsuno N, Uemura S, Oda S, Kondo M, Weerasinghe RW, Hu Y, Lestanto GNI, Tsuchiya Y, Li Y, Hatakeyama T, Adachi C. Bright, efficient, and stable pure-green hyperfluorescent organic light-emitting diodes by judicious molecular design. Nature Communications. 15: 3174. PMID 38609364 DOI: 10.1038/s41467-024-47482-3 |
0.501 |
|
| 2024 |
Ochi J, Yamasaki Y, Tanaka K, Kondo Y, Isayama K, Oda S, Kondo M, Hatakeyama T. Highly efficient multi-resonance thermally activated delayed fluorescence material toward a BT.2020 deep-blue emitter. Nature Communications. 15: 2361. PMID 38565868 DOI: 10.1038/s41467-024-46619-8 |
0.539 |
|
| 2023 |
Sano Y, Shintani T, Hayakawa M, Oda S, Kondo M, Matsushita T, Hatakeyama T. One-Shot Construction of BN-Embedded Heptadecacene Framework Exhibiting Ultra-narrowband Green Thermally Activated Delayed Fluorescence. Journal of the American Chemical Society. 145: 11504-11511. PMID 37192399 DOI: 10.1021/jacs.3c02873 |
0.596 |
|
| 2022 |
Uemura S, Oda S, Hayakawa M, Kawasumi R, Ikeda N, Lee YT, Chan CY, Tsuchiya Y, Adachi C, Hatakeyama T. Sequential Multiple Borylation Toward an Ultrapure Green Thermally Activated Delayed Fluorescence Material. Journal of the American Chemical Society. PMID 36547020 DOI: 10.1021/jacs.2c10946 |
0.555 |
|
| 2022 |
Oda S, Kawakami B, Horiuchi M, Yamasaki Y, Kawasumi R, Hatakeyama T. Ultra-Narrowband Blue Multi-Resonance Thermally Activated Delayed Fluorescence Materials. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2205070. PMID 36394083 DOI: 10.1002/advs.202205070 |
0.513 |
|
| 2022 |
Oda S, Kawakami B, Yamasaki Y, Matsumoto R, Yoshioka M, Fukushima D, Nakatsuka S, Hatakeyama T. Correction to "One-Shot Synthesis of Expanded Heterohelicene Exhibiting Narrowband Thermally Activated Delayed Fluorescence". Journal of the American Chemical Society. 144: 21426-21427. PMID 36366780 DOI: 10.1021/jacs.2c11135 |
0.502 |
|
| 2022 |
Okada N, Nakatsuka S, Kawasumi R, Gotoh H, Yasuda N, Hatakeyama T. Synthesis and Late-Stage Diversification of BN-Embedded Dibenzocorannulenes as Efficient Fluorescence Organic Light-Emitting Diode Emitters. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36260535 DOI: 10.1002/chem.202202627 |
0.327 |
|
| 2022 |
Oda S, Sugitani T, Tanaka H, Tabata K, Kawasumi R, Hatakeyama T. Development of Pure Green Thermally Activated Delayed Fluorescence Material by Cyano Substitution. Advanced Materials (Deerfield Beach, Fla.). e2201778. PMID 35726390 DOI: 10.1002/adma.202201778 |
0.537 |
|
| 2022 |
Oda S, Kawakami B, Yamasaki Y, Matsumoto R, Yoshioka M, Fukushima D, Nakatsuka S, Hatakeyama T. One-Shot Synthesis of Expanded Heterohelicene Exhibiting Narrowband Thermally Activated Delayed Fluorescence. Journal of the American Chemical Society. 144: 106-112. PMID 34941256 DOI: 10.1021/jacs.1c11659 |
0.551 |
|
| 2021 |
Tanaka H, Oda S, Ricci G, Gotoh H, Tabata K, Kawasumi R, Beljonne D, Olivier Y, Hatakeyama T. Hypsochromic Shift of Multiple-Resonance-Induced Thermally Activated Delayed Fluorescence by Oxygen Atom Incorporation. Angewandte Chemie (International Ed. in English). PMID 34038618 DOI: 10.1002/anie.202105032 |
0.513 |
|
| 2021 |
Matsui K, Oda S, Yoshiura K, Nakajima K, Yasuda N, Hatakeyama T. Correction to "One-Shot Multiple Borylation toward BN-Doped Nanographenes". Journal of the American Chemical Society. PMID 33449692 DOI: 10.1021/jacs.0c13373 |
0.447 |
|
| 2020 |
Oda S, Hatakeyama T, Kumano W, Hama T, Kawasumi R, Yoshiura K. Carbazole-Based DABNA Analogs as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light-Emitting Diodes. Angewandte Chemie (International Ed. in English). PMID 33180369 DOI: 10.1002/anie.202012891 |
0.567 |
|
| 2020 |
Ikeda N, Oda S, Matsumoto R, Yoshioka M, Fukushima D, Yoshiura K, Yasuda N, Hatakeyama T. Solution-Processable Pure Green Thermally Activated Delayed Fluorescence Emitter Based on the Multiple Resonance Effect. Advanced Materials (Deerfield Beach, Fla.). e2004072. PMID 32864797 DOI: 10.1002/Adma.202004072 |
0.581 |
|
| 2020 |
Nguyen TB, Nakanotani H, Hatakeyama T, Adachi C. The Role of Reverse Intersystem Crossing Using a TADF-Type Acceptor Molecule on the Device Stability of Exciplex-Based Organic Light-Emitting Diodes. Advanced Materials (Deerfield Beach, Fla.). e1906614. PMID 31975459 DOI: 10.1002/Adma.201906614 |
0.302 |
|
| 2020 |
Oda S, Ueura K, Kawakami B, Hatakeyama T. Multiple Electrophilic C-H Borylation of Arenes Using Boron Triiodide. Organic Letters. PMID 31908166 DOI: 10.1021/Acs.Orglett.9B04483 |
0.611 |
|
| 2019 |
Nakatsuka S, Watanabe Y, Kamakura Y, Horike S, Tanaka D, Hatakeyama T. Solvent-Vapor-Induced Reversible Single-Crystal-to-Single-Crystal Transformation of a Triphosphaazatriangulene-based Metal-Organic Framework. Angewandte Chemie (International Ed. in English). PMID 31773880 DOI: 10.1002/Anie.201912195 |
0.313 |
|
| 2019 |
Oda S, Kawakami B, Kawasumi R, Okita R, Hatakeyama T. Multiple Resonance-Effect-Induced Sky-Blue Thermally Activated Delayed Fluorescence with a Narrow Emission Band. Organic Letters. PMID 31613109 DOI: 10.1021/Acs.Orglett.9B03342 |
0.581 |
|
| 2019 |
Oda S, Shimizu T, Katayama T, Yoshikawa H, Hatakeyama T. Tetracoordinate Boron-Fused Double [5]Helicenes as Cathode Active Materials for Lithium Batteries. Organic Letters. PMID 30830790 DOI: 10.1021/Acs.Orglett.9B00337 |
0.573 |
|
| 2019 |
Agata R, Takaya H, Matsuda H, Nakatani N, Takeuchi K, Iwamoto T, Hatakeyama T, Nakamura M. Iron-Catalyzed Cross Coupling of Aryl Chlorides with Alkyl Grignard Reagents: Synthetic Scope and FeII/FeIV Mechanism Supported by X-ray Absorption Spectroscopy and Density Functional Theory Calculations Bulletin of the Chemical Society of Japan. 92: 381-390. DOI: 10.1246/Bcsj.20180333 |
0.592 |
|
| 2019 |
Kondo Y, Yoshiura K, Kitera S, Nishi H, Oda S, Gotoh H, Sasada Y, Yanai M, Hatakeyama T. Narrowband deep-blue organic light-emitting diode featuring an organoboron-based emitter Nature Photonics. 13: 678-682. DOI: 10.1038/S41566-019-0476-5 |
0.577 |
|
| 2018 |
Oda S, Abe H, Yasuda N, Hatakeyama T. Synthesis of Tetracoordinate Boron-Fused Benzoaceanthrylene Analogs via Tandem Electrophilic C-H Borylation. Chemistry, An Asian Journal. PMID 30548227 DOI: 10.1002/Asia.201801682 |
0.596 |
|
| 2018 |
Nakatsuka S, Yasuda N, Hatakeyama T. Four-Step Synthesis of BN-Embedded Corannulene. Journal of the American Chemical Society. PMID 30251839 DOI: 10.1021/Jacs.8B08197 |
0.304 |
|
| 2018 |
Gotoh H, Nakatsuka S, Kondo Y, Sasada Y, Hatakeyama T. Triangulene-based Efficient Exciton Blocking Material for Organic Light-emitting Diodes Chemistry Letters. 47: 920-922. DOI: 10.1246/Cl.180314 |
0.302 |
|
| 2018 |
Fukagawa H, Oono T, Iwasaki Y, Hatakeyama T, Shimizu T. High-efficiency ultrapure green organic light-emitting diodes Materials Chemistry Frontiers. 2: 704-709. DOI: 10.1039/C7Qm00588A |
0.302 |
|
| 2017 |
Matsui K, Oda S, Yoshiura K, Nakajima K, Yasuda N, Hatakeyama T. One-Shot Multiple Borylation toward BN-Doped Nanographenes. Journal of the American Chemical Society. PMID 29120174 DOI: 10.1021/Jacs.7B10578 |
0.62 |
|
| 2017 |
Nakatsuka S, Gotoh H, Kinoshita K, Yasuda N, Hatakeyama T. Divergent Synthesis of Heteroatom-Centered 4,8,12-Triazatriangulenes. Angewandte Chemie (International Ed. in English). 56: 5087-5090. PMID 28370999 DOI: 10.1002/Anie.201701246 |
0.382 |
|
| 2017 |
Nakatsuka S, Gotoh H, Kageyama A, Sasada Y, Ikuta T, Hatakeyama T. 5,9-Dioxa-13b-Oxophosphanaphtho[3,2,1-de]anthracenes Prepared by Tandem Phospha-Friedel–Crafts Reaction as Hole-/Exciton-Blocking Materials for OLEDs Organometallics. 36: 2622-2631. DOI: 10.1021/Acs.Organomet.7B00242 |
0.401 |
|
| 2017 |
Nakatsuka S, Gotoh H, Kinoshita K, Yasuda N, Hatakeyama T. Rücktitelbild: Divergent Synthesis of Heteroatom-Centered 4,8,12-Triazatriangulenes (Angew. Chem. 18/2017) Angewandte Chemie. 129: 5214-5214. DOI: 10.1002/Ange.201702884 |
0.343 |
|
| 2017 |
Nakanotani H, Furukawa T, Hosokai T, Hatakeyama T, Adachi C. Light Amplification in Molecules Exhibiting Thermally Activated Delayed Fluorescence Advanced Optical Materials. 5: 1700051. DOI: 10.1002/Adom.201700051 |
0.318 |
|
| 2016 |
Numano M, Nagami N, Nakatsuka S, Katayama T, Nakajima K, Tatsumi S, Yasuda N, Hatakeyama T. Synthesis of Boronate-Based Benzo[fg]tetracene and Benzo[hi]hexacene via Demethylative Direct Borylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 11574-7. PMID 27321480 DOI: 10.1002/Chem.201602753 |
0.376 |
|
| 2016 |
Katayama T, Nakatsuka S, Hirai H, Yasuda N, Kumar J, Kawai T, Hatakeyama T. Two-Step Synthesis of Boron-Fused Double Helicenes. Journal of the American Chemical Society. 138: 5210-3. PMID 27077723 DOI: 10.1021/Jacs.6B01674 |
0.414 |
|
| 2016 |
Hatakeyama T, Shiren K, Nakajima K, Nomura S, Nakatsuka S, Kinoshita K, Ni J, Ono Y, Ikuta T. Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO-LUMO Separation by the Multiple Resonance Effect. Advanced Materials (Deerfield Beach, Fla.). PMID 26865384 DOI: 10.1002/Adma.201505491 |
0.32 |
|
| 2015 |
Miyamoto F, Nakatsuka S, Yamada K, Nakayama KI, Hatakeyama T. Synthesis of Boron-Doped Polycyclic Aromatic Hydrocarbons by Tandem Intramolecular Electrophilic Arene Borylation. Organic Letters. PMID 26606580 DOI: 10.1021/Acs.Orglett.5B03167 |
0.339 |
|
| 2015 |
Hirai H, Nakajima K, Nakatsuka S, Shiren K, Ni J, Nomura S, Ikuta T, Hatakeyama T. One-Step Borylation of 1,3-Diaryloxybenzenes Towards Efficient Materials for Organic Light-Emitting Diodes. Angewandte Chemie (International Ed. in English). 54: 13581-5. PMID 26380959 DOI: 10.1002/Anie.201506335 |
0.401 |
|
| 2015 |
Nakagawa N, Hatakeyama T, Nakamura M. Iron-catalyzed diboration and carboboration of alkynes. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 4257-61. PMID 25631242 DOI: 10.1002/Chem.201406595 |
0.608 |
|
| 2015 |
Nakamura M, Aoki Y, Imayoshi R, Hatakeyama T, Takaya H. Synthesis of 2,7-Disubstituted 5,10-Diaryl-5,10-dihydrophenazines via Iron-Catalyzed Intramolecular Ring-Closing C–H Amination Heterocycles. 90: 893. DOI: 10.3987/Com-14-S(K)102 |
0.58 |
|
| 2015 |
Nakagawa N, Hatakeyama T, Nakamura M. Iron-catalyzed Suzuki-Miyaura coupling reaction of unactivated alkyl halides with lithium alkynylborates Chemistry Letters. 44: 486-488. DOI: 10.1246/Cl.141167 |
0.629 |
|
| 2015 |
Takaya H, Nakajima S, Nakagawa N, Isozaki K, Iwamoto T, Imayoshi R, Gower NJ, Adak L, Hatakeyama T, Honma T, Takagaki M, Sunada Y, Nagashima H, Hashizume D, Takahashi O, et al. Investigation of organoiron catalysis in Kumada-Tamao-Corriu-type cross-coupling reaction assisted by solution-phase X-ray absorption spectroscopy Bulletin of the Chemical Society of Japan. 88: 410-418. DOI: 10.1246/Bcsj.20140376 |
0.477 |
|
| 2015 |
Agata R, Iwamoto T, Nakagawa N, Isozaki K, Hatakeyama T, Takaya H, Nakamura M. Iron fluoride/N-heterocyclic carbene catalyzed cross coupling between deactivated aryl chlorides and alkyl grignard reagents with or without β-hydrogens Synthesis (Germany). 47: 1733-1740. DOI: 10.1055/S-0034-1380361 |
0.641 |
|
| 2015 |
Hatakeyama T, Ikuta T, Shiren K, Hashimoto S, Nakatsuka S, Hirai H, Nakajima K, Ni J, Nakamura M. 28.1:Invited Paper: Triplet-Energy Control of PAHs by Heteroatom Incorporation for Development of Efficient Materials for PHOLEDs Sid Symposium Digest of Technical Papers. 46: 401-403. DOI: 10.1002/sdtp.10370 |
0.361 |
|
| 2015 |
Nakagawa N, Hatakeyama T, Nakamura M. ChemInform Abstract: Iron-Catalyzed Suzuki-Miyaura Coupling Reaction of Unactivated Alkyl Halides with Lithium Alkynylborates. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201542085 |
0.429 |
|
| 2015 |
Agata R, Iwamoto T, Nakagawa N, Isozaki K, Hatakeyama T, Takaya H, Nakamura M. ChemInform Abstract: Iron Fluoride/N-Heterocyclic Carbene Catalyzed Cross Coupling Between Deactivated Aryl Chlorides and Alkyl Grignard Reagents with or without β-Hydrogens Cheminform. 46: no-no. DOI: 10.1002/chin.201542076 |
0.533 |
|
| 2015 |
Nakamura M, Aoki Y, Imayoshi R, Hatakeyama T, Takaya H. ChemInform Abstract: Synthesis of 2,7-Disubstituted 5,10-Diaryl-5,10-dihydrophenazines via Iron-Catalyzed Intramolecular Ring-Closing C-H Amination. Cheminform. 46: no-no. DOI: 10.1002/chin.201520207 |
0.509 |
|
| 2014 |
Hashimoto S, Nakatsuka S, Nakamura M, Hatakeyama T. Construction of a highly distorted benzene ring in a double helicene. Angewandte Chemie (International Ed. in English). 53: 14074-6. PMID 25319613 DOI: 10.1002/Anie.201408390 |
0.532 |
|
| 2014 |
Hatakeyama T, Hashimoto S, Nakamura M. Synthesis of Heteroatom-fused Polycyclic Aromatic Compounds via Tandem Hetero-Friedel-Crafts Reactions and Their Applications Journal of Synthetic Organic Chemistry, Japan. 72: 1391-1397. DOI: 10.5059/Yukigoseikyokaishi.72.1391 |
0.567 |
|
| 2014 |
Hashimoto S, Ikuta T, Shiren K, Nakatsuka S, Ni J, Nakamura M, Hatakeyama T. Triplet-Energy Control of Polycyclic Aromatic Hydrocarbons by BN Replacement: Development of Ambipolar Host Materials for Phosphorescent Organic Light-Emitting Diodes Chemistry of Materials. 26: 6265-6271. DOI: 10.1021/Cm503102D |
0.472 |
|
| 2013 |
Gabr RK, Hatakeyama T, Takenaka K, Takizawa S, Okada Y, Nakamura M, Sasai H. DFT study of a 5-endo-trig-type cyclization of 3-alkenoic acids by using Pd-spiro-bis(isoxazoline) as catalyst: importance of the rigid spiro framework for both selectivity and reactivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 9518-25. PMID 23749627 DOI: 10.1002/Chem.201203189 |
0.519 |
|
| 2013 |
Hatakeyama T, Hashimoto T, Kathriarachchi KKADS, Zenmyo T, Seike H, Nakamura M. ChemInform Abstract: Iron-Catalyzed Alkyl-Alkyl Suzuki-Miyaura Coupling. Cheminform. 44: no-no. DOI: 10.1002/chin.201305040 |
0.363 |
|
| 2013 |
Nakamura E, Hatakeyama T, Ito S, Ishizuka K, Ilies L, Nakamura M. Iron-Catalyzed Cross-Coupling Reactions Organic Reactions. 1-209. DOI: 10.1002/0471264180.Or083.01 |
0.794 |
|
| 2012 |
Hatakeyama T, Imayoshi R, Yoshimoto Y, Ghorai SK, Jin M, Takaya H, Norisuye K, Sohrin Y, Nakamura M. Iron-catalyzed aromatic amination for nonsymmetrical triarylamine synthesis. Journal of the American Chemical Society. 134: 20262-5. PMID 23181635 DOI: 10.1021/Ja309845K |
0.616 |
|
| 2012 |
Hatakeyama T, Hashimoto S, Oba T, Nakamura M. Azaboradibenzo[6]helicene: carrier inversion induced by helical homochirality. Journal of the American Chemical Society. 134: 19600-3. PMID 23167918 DOI: 10.1021/Ja310372F |
0.508 |
|
| 2012 |
Noda D, Sunada Y, Hatakeyama T, Nakamura M, Nagashima H. Iron promoted conjugate addition: implication of the six-centered mechanism based on the isolation of the iron-enolate intermediate. Chemical Communications (Cambridge, England). 48: 12231-3. PMID 23147813 DOI: 10.1039/C2Cc37144H |
0.528 |
|
| 2012 |
Hatakeyama T, Hashimoto T, Kathriarachchi KK, Zenmyo T, Seike H, Nakamura M. Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling. Angewandte Chemie (International Ed. in English). 51: 8834-7. PMID 22848024 DOI: 10.1002/Anie.201202797 |
0.594 |
|
| 2012 |
Ghorai SK, Jin M, Hatakeyama T, Nakamura M. Cross-coupling of non-activated chloroalkanes with aryl Grignard reagents in the presence of iron/N-heterocyclic carbene catalysts. Organic Letters. 14: 1066-9. PMID 22288653 DOI: 10.1021/Ol2031729 |
0.637 |
|
| 2012 |
Hashimoto T, Hatakeyama T, Nakamura M. Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by iron-bisphosphine complexes. The Journal of Organic Chemistry. 77: 1168-73. PMID 22148416 DOI: 10.1021/Jo202151F |
0.63 |
|
| 2012 |
Hatakeyama T, Ishizuka K, Nakamura M. ChemInform Abstract: Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms Cheminform. 43: no-no. DOI: 10.1002/CHIN.201215248 |
0.395 |
|
| 2012 |
Hatakeyama T, Fujiwara Y, Okada Y, Itoh T, Hashimoto T, Kawamura S, Ogata K, Takaya H, Nakamura M. ChemInform Abstract: Kumada-Tamao-Corriu Coupling of Alkyl Halides Catalyzed by an Iron-Bisphosphine Complex. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201208117 |
0.328 |
|
| 2011 |
Hatakeyama T, Hashimoto S, Seki S, Nakamura M. Synthesis of BN-fused polycyclic aromatics via tandem intramolecular electrophilic arene borylation. Journal of the American Chemical Society. 133: 18614-7. PMID 22026463 DOI: 10.1021/Ja208950C |
0.514 |
|
| 2011 |
Hatakeyama T, Okada Y, Yoshimoto Y, Nakamura M. Tuning chemoselectivity in iron-catalyzed Sonogashira-type reactions using a bisphosphine ligand with peripheral steric bulk: selective alkynylation of nonactivated alkyl halides. Angewandte Chemie (International Ed. in English). 50: 10973-6. PMID 21882321 DOI: 10.1002/Anie.201104125 |
0.596 |
|
| 2011 |
Hatakeyama T, Hashimoto S, Nakamura M. Tandem phospha-Friedel-Crafts reaction toward curved π-conjugated frameworks with a phosphorus ring junction. Organic Letters. 13: 2130-3. PMID 21434612 DOI: 10.1021/Ol200571S |
0.56 |
|
| 2011 |
Hatakeyama T, Ishizuka K, Nakamura M. Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms Journal of Synthetic Organic Chemistry, Japan. 69: 1282-1298. DOI: 10.5059/Yukigoseikyokaishi.69.1282 |
0.629 |
|
| 2011 |
Hatakeyama T, Fujiwara Y, Okada Y, Itoh T, Hashimoto T, Kawamura S, Ogata K, Takaya H, Nakamura M. Kumada–Tamao–Corriu Coupling of Alkyl Halides Catalyzed by an Iron–Bisphosphine Complex Chemistry Letters. 40: 1030-1032. DOI: 10.1246/Cl.2011.1030 |
0.566 |
|
| 2011 |
Hatakeyama T, Okada Y, Yoshimoto Y, Nakamura M. Rücktitelbild: Tuning Chemoselectivity in Iron-Catalyzed Sonogashira-Type Reactions Using a Bisphosphine Ligand with Peripheral Steric Bulk: Selective Alkynylation of Nonactivated Alkyl Halides (Angew. Chem. 46/2011) Angewandte Chemie. 123: 11204-11204. DOI: 10.1002/Ange.201106865 |
0.597 |
|
| 2010 |
Ishizuka K, Seike H, Hatakeyama T, Nakamura M. Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides. Journal of the American Chemical Society. 132: 13117-9. PMID 20815343 DOI: 10.1021/Ja104155F |
0.619 |
|
| 2010 |
Hatakeyama T, Hashimoto T, Kondo Y, Fujiwara Y, Seike H, Takaya H, Tamada Y, Ono T, Nakamura M. Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides. Journal of the American Chemical Society. 132: 10674-6. PMID 20681696 DOI: 10.1021/Ja103973A |
0.628 |
|
| 2010 |
Hatakeyama T, Yoshimoto Y, Ghorai SK, Nakamura M. Transition-metal-free electrophilic amination between aryl Grignard reagents and N-chloroamines. Organic Letters. 12: 1516-9. PMID 20222741 DOI: 10.1021/Ol100235B |
0.52 |
|
| 2010 |
Nakamura M, Ishizuka K, Seike H, Hatakeyama T. Alkenylative Cross-Coupling between Alkyl Sulfides and Grignard Reagents Synfacts. 2010: 1402-1402. DOI: 10.1055/S-0030-1258852 |
0.544 |
|
| 2010 |
Nakamura M, Hatakeyama T, Hashimoto T, Kondo Y, Fujiwara Y, Seike H, Takaya H, Tamada Y, Ono T. Iron-Catalyzed Suzuki-Miyaura Coupling Between Arylborates and Alkyl Halides Synfacts. 2010: 1290-1290. DOI: 10.1055/S-0030-1258703 |
0.588 |
|
| 2010 |
Hatakeyama T, Yoshimoto Y, Ghorai SK, Nakamura M. Transition-Metal-Free Amination of Aryl Grignard Reagents Synfacts. 2010: 821-821. DOI: 10.1055/S-0029-1220051 |
0.46 |
|
| 2010 |
Hatakeyama T, Nakagawa N, Nakamura M. Iron-Catalyzed sp²-sp³ Cross-Couplingof Alkenylzinc Compounds Synfacts. 2010: 89-89. DOI: 10.1055/S-0029-1218427 |
0.382 |
|
| 2009 |
Hatakeyama T, Nakagawa N, Nakamura M. Iron-catalyzed Negishi coupling toward an effective olefin synthesis. Organic Letters. 11: 4496-9. PMID 19757826 DOI: 10.1021/Ol901555R |
0.646 |
|
| 2009 |
Hatakeyama T, Hashimoto S, Ishizuka K, Nakamura M. Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides. Journal of the American Chemical Society. 131: 11949-63. PMID 19639999 DOI: 10.1021/Ja9039289 |
0.596 |
|
| 2009 |
Noda D, Sunada Y, Hatakeyama T, Nakamura M, Nagashima H. Effect of TMEDA on iron-catalyzed coupling reactions of ArMgX with alkyl halides. Journal of the American Chemical Society. 131: 6078-9. PMID 19364096 DOI: 10.1021/Ja901262G |
0.618 |
|
| 2009 |
Hatakeyama T, Kondo Y, Fujiwara Y, Takaya H, Ito S, Nakamura E, Nakamura M. Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene. Chemical Communications (Cambridge, England). 1216-8. PMID 19240878 DOI: 10.1039/B820879D |
0.731 |
|
| 2009 |
Noda D, Sunada Y, Hatakeyama T, Nakamura M, Nagashima H. Role of TMEDA in Iron-Catalyzed Coupling Reactions Synfacts. 2009: 751-751. DOI: 10.1055/S-0029-1217283 |
0.608 |
|
| 2008 |
Hatakeyama T, Yoshimoto Y, Gabriel T, Nakamura M. Iron-catalyzed enyne cross-coupling reaction. Organic Letters. 10: 5341-4. PMID 18986153 DOI: 10.1055/S-0028-1087702 |
0.656 |
|
| 2008 |
Hatakeyama T, Nakamura M, Nakamura E. Diastereoselective addition of zincated hydrazones to alkenylboronates and stereospecific trapping of boron/zinc bimetallic intermediates by carbon electrophiles. Journal of the American Chemical Society. 130: 15688-701. PMID 18950158 DOI: 10.1021/Ja806258V |
0.633 |
|
| 2007 |
Hatakeyama T, Nakamura M. Iron-catalyzed selective biaryl coupling: remarkable suppression of homocoupling by the fluoride anion. Journal of the American Chemical Society. 129: 9844-5. PMID 17658810 DOI: 10.1021/Ja073084L |
0.609 |
|
| 2007 |
Endo K, Hatakeyama T, Nakamura M, Nakamura E. Indium-catalyzed 2-alkenylation of 1,3-dicarbonyl compounds with unactivated alkynes. Journal of the American Chemical Society. 129: 5264-71. PMID 17388598 DOI: 10.1021/Ja0702014 |
0.748 |
|
| 2007 |
Hatakeyama T, Ito S, Yamane H, Nakamura M, Nakamura E. Regioselective α-alkylation of ketones with alkyl chlorides and fluorides via highly nucleophilic magnesium enamides Tetrahedron. 63: 8440-8448. DOI: 10.1016/J.Tet.2007.05.087 |
0.713 |
|
| 2007 |
Hatakeyama T, Ito S, Yamane H, Nakamura M, Nakamura E. Regioselective α-Alkylation of Ketones with Alkyl Chlorides and Fluorides via Highly Nucleophilic Magnesium Enamides. Cheminform. 38. DOI: 10.1002/chin.200750049 |
0.583 |
|
| 2006 |
Hatakeyama T, Chen DL, Ismagilov RF. Microgram-scale testing of reaction conditions in solution using nanoliter plugs in microfluidics with detection by MALDI-MS Journal of the American Chemical Society. 128: 2518-2519. PMID 16492019 DOI: 10.1021/Ja057720W |
0.348 |
|
| 2005 |
Hatakeyama T, Ito S, Nakamura M, Nakamura E. Alkylation of magnesium enamide with alkyl chlorides and fluorides. Journal of the American Chemical Society. 127: 14192-3. PMID 16218607 DOI: 10.1021/Ja055306Q |
0.704 |
|
| 2004 |
Nakamura M, Hatakeyama T, Hara K, Fukudome H, Nakamura E. Sequential coupling of zincated hydrazone, alkenylboronate, and electrophile that creates several contiguous stereogenic centers. Journal of the American Chemical Society. 126: 14344-5. PMID 15521740 DOI: 10.1021/Ja044878S |
0.712 |
|
| 2004 |
Nakamura M, Hatakeyama T, Nakamura E. Alpha-alkylation of ketones by addition of zinc enamides to unactivated olefins. Journal of the American Chemical Society. 126: 11820-5. PMID 15382916 DOI: 10.1021/Ja0465193 |
0.604 |
|
| 2003 |
Nakamura M, Hatakeyama T, Hara K, Nakamura E. Enantioselective synthesis of alpha-substituted ketones by asymmetric addition of chiral zinc enamides to 1-alkenes. Journal of the American Chemical Society. 125: 6362-3. PMID 12785764 DOI: 10.1021/Ja035091P |
0.713 |
|
| 2001 |
Nakamura M, Hara K, Hatakeyama T, Nakamura E. Regioselective allylzincation of alkenylboronate. Organic Letters. 3: 3137-40. PMID 11574014 DOI: 10.1021/Ol0164637 |
0.714 |
|
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