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Hao-Sheng Lin - Publications

Affiliations: 
2014-2017 Nagoya University, Nagoya-shi, Aichi-ken, Japan 
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7 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
2020 Yan XX, Li B, Lin HS, Jin F, Niu C, Liu KQ, Wang GW, Yang S. Successively Regioselective Electrosynthesis and Electron Transport Property of Stable Multiply Functionalized [60]Fullerene Derivatives. Research (Washington, D.C.). 2020: 2059190. PMID 32149279 DOI: 10.34133/2020/2059190  0.487
2019 Yang XY, Lin HS, Matsuo Y. Highly selective synthesis of tetrahydronaphthaleno[60]fullerenes via fullerene-cation-mediated intramolecular cyclization. The Journal of Organic Chemistry. PMID 31742406 DOI: 10.1021/Acs.Joc.9B02618  0.417
2018 Lin HS, Matsuo Y. Functionalization of [60]fullerene through fullerene cation intermediates. Chemical Communications (Cambridge, England). PMID 30206580 DOI: 10.1039/C8Cc05965A  0.462
2018 Yang XY, Lin HS, Jeon I, Matsuo Y. Fullerene-Cation-Mediated Noble-Metal-Free Direct Introduction of Functionalized Aryl Groups onto [60]Fullerene. Organic Letters. PMID 29763329 DOI: 10.1021/Acs.Orglett.8B01295  0.314
2017 Jing K, Yao JP, Li ZY, Li QL, Lin HS, Wang GW. Palladium-Catalyzed Decarboxylative ortho-Acylation of Benzamides with α-Oxocarboxylic Acids. The Journal of Organic Chemistry. PMID 29124923 DOI: 10.1021/acs.joc.7b02552  0.491
2017 Xu H, Liu HW, Lin HS, Wang GW. Solvent-free iodine-promoted synthesis of 3,2'-pyrrolinyl spirooxindoles from alkylidene oxindoles and enamino esters under ball-milling conditions. Chemical Communications (Cambridge, England). PMID 29105709 DOI: 10.1039/c7cc08306h  0.452
2017 Wang JJ, Lin HS, Niu C, Wang GW. The cyclopropanation of [60]fullerobenzofurans via electrosynthesis. Organic & Biomolecular Chemistry. PMID 28345692 DOI: 10.1039/c7ob00463j  0.472
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