Benjamin List 研究室
主宰者：Benjamin List
北海道大学
AI 要約（直近 5 年の研究成果）
要約はまだ生成されていません。
※ AI（Claude）が、公開されている論文要旨から研究の問い・手法・主要な発見を事実情報として抽出・再構成して自動生成しています。誤りを含む可能性があるため、正確性は研究室公式情報でご確認ください。
外部リンク
関連研究室(8 件)
- 計算機科学Jiyi Li 研究室北海道大学論文 57 件·共通: mRNA, 翻訳・RNA代謝, RNA生物学分野, 遺伝子発現制御 +8
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- 材料科学Yasuchika Hasegawa 研究室北海道大学論文 88 件·共通: VR・AR, 視覚メディア工学, 視覚・音メディア, ヒューマン・メディア情報 +8
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研究成果（100 件）
- DOI: https://doi.org/10.1021/jacs.6c01167
- DOI: https://doi.org/10.1021/acscatal.5c03020
- DOI: https://doi.org/10.1021/jacs.5c08345
- DOI: https://doi.org/10.1055/a-2616-6753
- DOI: https://doi.org/10.1021/jacs.5c11514
- DOI: https://doi.org/10.1021/jacs.5c11553
- DOI: https://doi.org/10.1021/jacs.4c18485
- DOI: https://doi.org/10.1021/jacs.4c18378
- DOI: https://doi.org/10.1038/s41467-025-58313-4
- DOI: https://doi.org/10.1021/acscatal.5c02225
続きを表示（残り 90 件）閉じる
- DOI: https://doi.org/10.1021/jacs.5c00641
- DOI: https://doi.org/10.1038/s41929-025-01340-7
- DOI: https://doi.org/10.1038/s41586-025-09905-z
- [2025] Pericyclic Umpolung in a Catalytic Asymmetric Diels–Alder Reaction of Tropone with Enol EthersDOI: https://doi.org/10.1021/jacs.5c05709
- DOI: https://doi.org/10.1021/jacs.5c13725
- DOI: https://doi.org/10.1055/s-0043-1763900
- DOI: https://doi.org/10.1055/s-0043-1763901
- [2024] Diazaphospholene Hydrides Catalyze Enantioselective Reductive Eschenmoser–Claisen RearrangementsDOI: https://doi.org/10.1055/s-0043-1763897
- DOI: https://doi.org/10.1055/s-0043-1763899
- DOI: https://doi.org/10.1055/s-0043-1763877
- DOI: https://doi.org/10.1055/s-0043-1773117
- DOI: https://doi.org/10.1055/s-0043-1773112
- DOI: https://doi.org/10.1055/s-0043-1773114
- DOI: https://doi.org/10.1055/s-0043-1773119
- DOI: https://doi.org/10.1055/s-0043-1773118
- DOI: https://doi.org/10.1055/s-0043-1773113
- DOI: https://doi.org/10.1055/s-0043-1773116
- DOI: https://doi.org/10.1055/s-0043-1773115
- [2024] Catalytic Asymmetric Cycloaddition of Olefins with In Situ Generated <i>N</i>-Boc-FormaldimineDOI: https://doi.org/10.1021/jacs.4c13538
- [2024] Hydrodeamination through in situ Generation of Diazonium Species by ortho-Naphthoquinone CatalysisDOI: https://doi.org/10.1055/s-0043-1775220
- [2024] Photocatalysis Enables the Hydroamidation of Alkenes Using Sulfonyl Azides and Hantzsch EstersDOI: https://doi.org/10.1055/s-0043-1775219
- DOI: https://doi.org/10.1055/s-0043-1775212
- [2024] Stereodivergent Radical Cyclizations Enabled by Directed Evolution of Fatty Acid PhotodecarboxylasesDOI: https://doi.org/10.1055/s-0043-1775213
- DOI: https://doi.org/10.1055/s-0043-1775210
- [2024] Enantioselective C−C Bond Insertion into Aldehydes via Oxazaborolidinium Catalyzed 1,2-Acyl ShiftDOI: https://doi.org/10.1055/s-0043-1773120
- DOI: https://doi.org/10.1126/science.adp9061
- DOI: https://doi.org/10.1055/s-0043-1774832
- DOI: https://doi.org/10.1055/s-0043-1774839
- DOI: https://doi.org/10.1055/s-0043-1774833
- DOI: https://doi.org/10.1055/s-0043-1774835
- DOI: https://doi.org/10.1055/s-0043-1774840
- DOI: https://doi.org/10.1055/s-0043-1774838
- DOI: https://doi.org/10.1055/s-0043-1774836
- DOI: https://doi.org/10.1055/s-0043-1774841
- DOI: https://doi.org/10.1055/s-0043-1763903
- DOI: https://doi.org/10.1055/s-0043-1763904
- [2024] Flavin-Photocatalytic Sulfide α-C–H Functionalization Using Arylsulfonyl Multiple-Bond ReagentsDOI: https://doi.org/10.1055/s-0043-1763905
- DOI: https://doi.org/10.1055/s-0043-1763898
- DOI: https://doi.org/10.1055/s-0043-1763902
- [2024] Cooperative Photoredox and Chiral Brønsted Acid Catalysis Permits Asymmetric [2π+2σ] CycloadditionDOI: https://doi.org/10.1055/s-0043-1774837
- DOI: https://doi.org/10.1055/s-0043-1774834
- DOI: https://doi.org/10.1021/jacs.4c09421
- [2024] A solid noncovalent organic double-helix framework catalyzes asymmetric [6 + 4] cycloadditionDOI: https://doi.org/10.1126/science.adp1127
- DOI: https://doi.org/10.1038/s41586-024-07757-7
- DOI: https://doi.org/10.1055/s-0043-1775239
- DOI: https://doi.org/10.1055/s-0043-1775234
- [2024] Lysine as a ‘Smart’ Amine Donor for Transaminase-Catalyzed Synthesis of β-Branched Amino AcidsDOI: https://doi.org/10.1055/s-0043-1775237
- DOI: https://doi.org/10.1038/s41467-024-49988-2
- DOI: https://doi.org/10.1055/s-0043-1775214
- [2024] N-Heterocyclic Carbenes Catalyze the Formation of Fused 6-5-5 Tricyclic Natural-Product FrameworksDOI: https://doi.org/10.1055/s-0043-1775216
- DOI: https://doi.org/10.1055/s-0043-1775217
- DOI: https://doi.org/10.1038/s41586-023-06826-7
- DOI: https://doi.org/10.1021/acscatal.3c05342
- [2023] Stereoselective Synthesis of Cyclopropane Derivatives from Mixtures of (E)- and (Z)-Enol AcetatesDOI: https://doi.org/10.1055/s-0042-1752028
- DOI: https://doi.org/10.1055/s-0042-1752031
- DOI: https://doi.org/10.1055/s-0042-1752035
- DOI: https://doi.org/10.1055/s-0042-1752029
- DOI: https://doi.org/10.1002/ckon.202300044
- [2023] Direct, Additive-Free Electrochemical Dehydrative Esterification of Carboxylic Acids and AlcoholsDOI: https://doi.org/10.1055/s-0042-1752225
- DOI: https://doi.org/10.1055/s-0042-1752229
- DOI: https://doi.org/10.1055/s-0042-1752226
- DOI: https://doi.org/10.1055/s-0042-1752227
- DOI: https://doi.org/10.1055/s-0042-1752228
- [2023] Cytochrome P450-Derived Ketone Synthase Enables Regioselective Aerobic Oxidation of ArylalkenesDOI: https://doi.org/10.1055/s-0042-1752223
- DOI: https://doi.org/10.1055/s-0043-1763840
- DOI: https://doi.org/10.1055/s-0043-1763839
- [2023] Enantioselective C–C, C–O and C–N Bond Formation with Intermediacy of a Benzylic Secondary CationDOI: https://doi.org/10.1055/s-0043-1763836
- [2023] Photocatalytic syn-Selective Thioalkynylation, Thiovinylation and Thioallylation of BicyclobutanesDOI: https://doi.org/10.1055/s-0043-1763834
- [2023] Ene-Reductase: Catalyst for the Photoenzymatic Stereoselective Synthesis of Benzo-Fused HeterocyclesDOI: https://doi.org/10.1055/s-0043-1763838
- DOI: https://doi.org/10.1055/s-0043-1763833
- DOI: https://doi.org/10.1055/s-0043-1763835
- DOI: https://doi.org/10.1055/s-0043-1763837
- DOI: https://doi.org/10.1055/s-0043-1763841
- DOI: https://doi.org/10.1055/s-0043-1763842
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.81.1019
- DOI: https://doi.org/10.1126/science.adj7007
- DOI: https://doi.org/10.1055/s-0042-1751973
- [2023] CO2 Reduction by a Membranous, Metal-Free, Triazine- and Imine-Containing Covalent Organic FrameworkDOI: https://doi.org/10.1055/s-0042-1751974
- [2023] Bifunctional Iminophosphorane Catalyst Enables Challenging Intramolecular Oxa-Michael ReactionsDOI: https://doi.org/10.1055/s-0042-1751975
- DOI: https://doi.org/10.1055/s-0042-1751968
- DOI: https://doi.org/10.1055/s-0042-1751970
- DOI: https://doi.org/10.1055/s-0042-1751972
- [2023] Enantioselective Nucleophilic Desymmetrization of Phosphonate Esters Using Bifunctional SuperbasesDOI: https://doi.org/10.1055/s-0042-1751967
- DOI: https://doi.org/10.1055/s-0042-1751969
- [2023] Biocatalysis and Photocatalysis Joining Forces in a Stereoselective Method for Synthesis of SulfonesDOI: https://doi.org/10.1055/s-0042-1751971
- DOI: https://doi.org/10.1055/s-0042-1752222
- DOI: https://doi.org/10.1055/s-0042-1752224
- DOI: https://doi.org/10.1055/s-0042-1752032
- DOI: https://doi.org/10.1055/s-0042-1752027
- [2023] Asymmetric [2+2] Photocycloaddition to Truxinates by Brønsted Acid-Catalyzed Chromophore ActivationDOI: https://doi.org/10.1055/s-0042-1752033
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