Sobi Asako - Publications

Affiliations: 
Okayama University, Okayama-shi, Okayama-ken, Japan 

21/24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Di Giovannantonio M, Qiu Z, Pignedoli CA, Asako S, Ruffieux P, Müllen K, Narita A, Fasel R. On-surface cyclization of vinyl groups on poly-para-phenylene involving an unusual pentagon to hexagon transformation. Nature Communications. 15: 1910. PMID 38429274 DOI: 10.1038/s41467-024-46173-3  0.335
2022 Banerjee S, Kobayashi T, Takai K, Asako S, Ilies L. Molybdenum-Quinone-Catalyzed Deoxygenative Coupling of Aromatic Carbonyl Compounds. Organic Letters. PMID 36166349 DOI: 10.1021/acs.orglett.2c03143  0.355
2022 Ramadoss B, Jin Y, Asako S, Ilies L. Remote steric control for undirected -selective C-H activation of arenes. Science (New York, N.Y.). 375: 658-663. PMID 35143323 DOI: 10.1126/science.abm7599  0.336
2020 Asako S, Ilies L. Olefin Synthesis by Deoxygenative Coupling of Carbonyl Compounds: From Stoichiometric to Catalytic Chemistry Letters. DOI: 10.1246/Cl.200540  0.381
2019 Asako S, Ishihara S, Hirata K, Takai K. Deoxygenative Insertion of Carbonyl Carbon into a C(sp3)-H Bond: Synthesis of Indolines and Indoles. Journal of the American Chemical Society. PMID 31184481 DOI: 10.1021/Jacs.9B05428  0.512
2019 Asako S, Kodera M, Nakajima H, Takai K. Lithium‐Free Synthesis of Sodium 2,2,6,6‐Tetramethylpiperidide and Its Synthetic Applications Advanced Synthesis & Catalysis. 361: 3120-3123. DOI: 10.1002/Adsc.201900215  0.308
2018 Asako S, Kobashi T, Takai K. Use of Cyclopropane as C1 Synthetic Unit by Directed Retro-Cyclopropanation with Ethylene Release. Journal of the American Chemical Society. PMID 30347153 DOI: 10.1021/Jacs.8B09297  0.511
2017 Murai M, Okada R, Asako S, Takai K. Rhodium-Catalyzed Silylative and Germylative Cyclization with Dehydrogenation Leading to 9-Sila- and 9-Germafluorenes: A Combined Experimental and Computational Mechanistic Study. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28557136 DOI: 10.1002/Chem.201701579  0.512
2016 Asako S, Ishikawa S, Takai K. Synthesis of Linear Allylsilanes via Molybdenum-Catalyzed Regioselective Hydrosilylation of Allenes Acs Catalysis. 6: 3387-3395. DOI: 10.1021/Acscatal.6B00627  0.488
2016 Asako S, Sakae T, Murai M, Takai K. Molybdenum-Catalyzed Stereospecific Deoxygenation of Epoxides to Alkenes Advanced Synthesis & Catalysis. 358: 3966-3970. DOI: 10.1002/Adsc.201600840  0.529
2015 Ilies L, Ichikawa S, Asako S, Matsubara T, Nakamura E. ChemInform Abstract: Iron-Catalyzed Directed Alkylation of Alkenes and Arenes with Alkylzinc Halides. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201548060  0.415
2015 Ilies L, Ichikawa S, Asako S, Matsubara T, Nakamura E. Iron-Catalyzed Directed Alkylation of Alkenes and Arenes with Alkylzinc Halides Advanced Synthesis and Catalysis. 357: 2175-2179. DOI: 10.1002/Adsc.201500276  0.563
2014 Shang R, Ilies L, Asako S, Nakamura E. Iron-catalyzed C(sp(2))-H bond functionalization with organoboron compounds. Journal of the American Chemical Society. 136: 14349-52. PMID 25268693 DOI: 10.1021/Ja5070763  0.527
2014 Ilies L, Matsubara T, Ichikawa S, Asako S, Nakamura E. Iron-catalyzed directed alkylation of aromatic and olefinic carboxamides with primary and secondary alkyl tosylates, mesylates, and halides. Journal of the American Chemical Society. 136: 13126-9. PMID 25032786 DOI: 10.1021/Ja5066015  0.522
2014 Matsubara T, Asako S, Ilies L, Nakamura E. Synthesis of anthranilic acid derivatives through iron-catalyzed ortho amination of aromatic carboxamides with N-chloroamines. Journal of the American Chemical Society. 136: 646-9. PMID 24380435 DOI: 10.1021/Ja412521K  0.514
2014 Asako S, Ilies L, Verma P, Ichikawa S, Nakamura E. Theoretical study on alkoxydiphosphine ligand for bimetallic cooperation in nickel-catalyzed monosubstitution of CF bond Chemistry Letters. 43: 726-728. DOI: 10.1246/Cl.131205  0.347
2014 Asako S, Norinder J, Ilies L, Yoshikai N, Nakamura E. ChemInform Abstract: ortho-Allylation of 1-Arylpyrazoles with Allyl Phenyl Ether via Iron-Catalyzed C-H Bond Activation under Mild Conditions. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201442138  0.471
2014 Asako S, Norinder J, Ilies L, Yoshikai N, Nakamura E. Ortho-allylation of 1-arylpyrazoles with allyl phenyl ether via iron-catalyzed C-H bond activation under mild conditions Advanced Synthesis and Catalysis. 356: 1481-1485. DOI: 10.1002/Adsc.201400063  0.502
2013 Asako S, Ilies L, Nakamura E. Iron-catalyzed ortho-allylation of aromatic carboxamides with allyl ethers. Journal of the American Chemical Society. 135: 17755-7. PMID 24215539 DOI: 10.1021/Ja4106368  0.559
2011 Yoshikai N, Asako S, Yamakawa T, Ilies L, Nakamura E. Iron-catalyzed C-H bond activation for the ortho-arylation of aryl pyridines and imines with Grignard reagents. Chemistry, An Asian Journal. 6: 3059-65. PMID 21898839 DOI: 10.1002/Asia.201100470  0.602
2011 Ilies L, Asako S, Nakamura E. Iron-catalyzed stereospecific activation of olefinic C-H bonds with Grignard reagent for synthesis of substituted olefins. Journal of the American Chemical Society. 133: 7672-5. PMID 21524107 DOI: 10.1021/Ja2017202  0.601
Low-probability matches (unlikely to be authored by this person)
2021 Asako S, Takahashi I, Nakajima H, Ilies L, Takai K. Halogen-sodium exchange enables efficient access to organosodium compounds. Communications Chemistry. 4: 76. PMID 36697639 DOI: 10.1038/s42004-021-00513-2  0.288
2020 Qiu Z, Asako S, Hu Y, Ju CW, Liu T, Rondin L, Schollmeyer D, Lauret JS, Müllen K, Narita A. Negatively Curved Nanographene with Heptagonal and [5]Helicene Units. Journal of the American Chemical Society. PMID 32809808 DOI: 10.1021/Jacs.0C05504  0.245
2019 Asako S, Nakajima H, Takai K. Organosodium compounds for catalytic cross-coupling Nature Catalysis. 2: 297-303. DOI: 10.1038/s41929-019-0250-6  0.169
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