Lewis acid-catalyzed formal 1,3-aminomethyl migration, Shibata, S.; Amano, K.; Kojima, T. Mori, K.Chem. Commun., 2023, 59, 9976–9979.
Diarylmethylamine (“Butterfly”-type amine) unit: a useful unit for the modulation of catalytic activity of aminothiourea catalysts, Ogawa, H.; Okawa, H.; Mori, K.Synlett, 2023, 1899–1904.
Hydride Shift Mediated C(sp3)-H Bond Functionalization (Internal Redox Reaction), Mori, K. Akiyama, T. J. Synth. Org. Chem., 2023, 81, 582?–593.
Direct access to 9/6-fused cycles via sequential hydride shift mediated double C(sp3)–H bond functionalization, Nakamura, I.; Anada, M.; Sueki, S.; Makino, K.; Mori, K.Adv. Synth. Catal., 2023, 365, 502–507.
Hydride shift mediated C(sp3)–H bond functionalization starting from non-aniline/phenol type substrates: evolution into a sequential system, Mori, K.; Okawa, H. Tetrahedron Lett., 2022, 110, 154178.
Access to ortho-Hydroxyphenyl Ketimines via Imine Anion-mediated Smiles Rearrangement, Jinno, S.; Senoo, T.; Mori, K.Org. Lett., 2022, 24, 4140?–4144.
“Stacked-arene”-type organocatalysts: utilization of pi-pi interaction as an electron tuning tool, Yamamoto, Y.; Inoue, A.; Sakai, D.; Ootawa, Y.; Mori, K.Tetrahedron Lett., 2022, 84, 153921.
Synthesis of C3-Symmetric Macrocyclic Triimines from Monomers having Boc-Protected Amine and Formyl Group, Moriya, Y.; Yamanaka, M.; Mori, K.Chem. Lett.,2022, 51, 217?–220.
C(sp3)–H Bond Functionalization Mediated by Hydride Shift/Cyclization System (Award account), Mori, K.Bull. Chem. Soc. Jpn., 2022, 95, 296?–305.
Divergent Access to Seven/Five-Membered Rings Based on [1,6]-Hydride Shift/Cyclization Process, Hoshino, D. Mori, K.Org. Lett., 2021, 23, 9403?–9407.
Stereoselective synthesis of highly congested tetralin-fused spirooxindoles with hydroxy group: pseudo oxygen atom induced hydride shift/cyclization process, Sakai, D. Machida, M.; Mori, K.Tetrahedron Lett., 2021, 83, 153408.
Rapid access to 3-indolyl-1-trifluoromethyl-isobenzofurans by hybrid use of Lewis/Br?nsted acid catalysts, Hoshino, D.; Mori, K.Org. Biomol. Chem., 2020, 18, 6602?–6606.
Genome Mining-Based Discovery of Fungal Macrolides Modified by GPI-Ethanolamine Phosphate Transferase Homologs, Morishita, Y.; Aoki, Y.; Ito, M.; Hagiwara, D.; Kuroda, T.; Fukano, H.; Hoshino, Y.; Suzuki, M.; Taniguchi, T.; Mori, K.; Asai, T. Org. Lett., 2020, 22, 5876?–5879.
Highly Stereoselective Synthesis of Fused Tetrahydropyrans via Lewis-Acid-Promoted Double C(sp3)–H Bond Functionalization, Yokoo, K.; Sakai, D.; Mori, K.Org. Lett., 2020, 22, 5801?–5805.
Facile Synthesis of π-Conjugated Heteroaromatic Compounds via Weak-Base-Promoted Transition-Metal-Free C–N Coupling, Senoo, T.; Inoue, A.; Mori, K.Synthesis, 2020, 56, 1096?–1102.
Expeditious Synthesis of Multi-Substituted Quinolinone Derivatives Based on Ring Recombination Strategy Yokoo, K.; Mori, K.Org. Lett.,2020, 22, 244?–248.
Highly Diastereoselective Synthesis of Medium-Sized Carbocycle Fused Piperidines via Sequential Hydride Shift Triggered Double C(sp3)–H Bond Functionalization, Kataoka, M.; Otawa, Y.; Ido, N.; Mori, K.;Org. Lett.2019, 21, 9334?–9338.
Construction of Seven- and Eight-Membered Carbocycles by Lewis Acid Catalyzed C(sp3)–H Bond Functionalization, Otawa, Y.; Mori, K.Chem. Commun.2019, 55 13856?–13859.
Discovery of Fungal Polyene Macrolides via Post-Genomic Approach Reveals a Polyketide Macrocyclization by trans-Acting Thioesterase in Fungi, Morishita, Y.; Zhang, H.-P..; Taniguchi, T.; Mori, K.; Asai, T. Org. Lett., 2019, 21, 4788?–4792.
Synthesis of Seven-Membered Ring Containing Difluoromethylene Unitby Sc(OTf)3-Catalyzed Activation of Single C–F Bond in CF3 Group, Hisano, N.; Kimura, D.; Mori, K.Chem. Lett.2019, 48, 771?–774.
Diastereoselective Synthesis of CF3-substituted Spiroisochromans by [1,5]-Hydride Shift/Cyclization/Intramolecular Friedel-Crafts Reaction Sequence, Tamura, R.; Kitamura, E.; Tsutsumi, R.; Yamanaka, M; Akiyama, T.; Mori, K.Org. Lett.2019, 21, 2383?–2387.
Diastereoselective Synthesis of Multisubstituted Chroman Derivatives via Iminium Formation/Morita-Baylis-Hillman Reaction/Oxa-Michael Reaction Sequence, Ido, N. Mori, K.Chem. Lett.2019, 48, 337?–340.
Expeditious Synthesis of Multisubstituted Indoles via Multiple Hydrogen Transfers, Yoshida, T. Mori, K.Chem. Commun.2018, 54, 12686?–12689.
Construction of 1,3-Dithio-Substituted Tetralins by [1,5]-Alkylthio Group Transfer Mediated Skeletal Rearrangement, Hisano, N.; Kamei, Y.; Kansaku, Y.; Yamanaka, M.; Mori, K.Org. Lett.2018, 20, 4223?–4226.
Highly Diastereoselective Synthesis of Tricyclic Fused-Pyrans by Sequential Hydride Shift Mediated Double C(sp3)–H Bond Functionalization, Mori, K.; Umehara, N.; Akiyama, T. Chem. Sci.2018, 9, 7327?–7331.
Divergent Synthesis of CF3-Substituted Polycyclic Skeltons Based on Control of Activation Site of Acid Catalysts, Yokoo, K. Mori, K.;Chem. Commun.2018, 54, 6927?–6930.
Chiral Magnesium Bisphosphate Catalyzed Asymmetric Double C(sp3)–H Bond Functionalization Based on Sequential Hydride Shift/Cyclization Process, Mori, K.; Isogai, R.; Kamei, Y.; Yamanaka, M.; Akiyama, T. J. Am. Chem. Soc.2018, 140, 6203?–6207.
Highly Diastereoselective Synthesis of Tetralin-Fused Spirooxindoles via Lewis Acid-Catalyzed C(sp3)–H Bond Functionalization, Machida, M. Mori, K.Chem. Lett.2018, 47, 868?–871.
Hf(OTf)4-Catalyzed highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via benzylic C(sp3)–H bond functionalization, Yoshida, T. Mori, K.Chem. Commun.2017, 53, 4319?–4322.
Highly Efficient Kinetic Resolution of PHANOL by Chiral Phosphoric Acid Catalyzed Asymmetric Acylation, Mori, K.; Kishi, H.; Akiyama, T. Synthesis2017, 365?–370.
Enantiodivergent Atroposelective Synthesis of Chiral Biaryls by Asymmetric Transfer Hydrogenation: Chiral Phosphoric Acid Catalyzed Dynamic Kinetic Resolution, Mori, K.; Itakura, T.; Akiyama, T. Angew. Chem. Int. Ed.2016, 55, 11642?–11646.
Enantioselective Synthesis of Fused Heterocycles with Contiguous Stereogenic Centers by Chiral Phosphoric Acid Catalyzed Symmetry Breaking, Mori, K.; Miyake, A.; Akiyama, T. Chem. Commun.2015, 51, 16107?–16110.
Synthesis of 3-Aryl-1-trifluoromethyltetrahydroisoquinolines by Br?nsted Acid Catalyzed C(sp3)–H Bond Functionalization, Mori, K.; Umehara, N.; Akiyama, T. Adv. Synth. Catal.2015, 357, 901–906. (Selected as an vip and front cover article).
Enantioselective Synthesis of Chiral Biaryl Chlorides/Iodides by a Chiral Phosphoric Acid Catalyzed Sequential Halogenation Strategy, Mori, K.; Kobayashi, M.; Itakura, T.; Akiyama, T. Adv. Synth. Catal.2015, 357, 35–40.
Stereoselective Construction of All Carbon Quaternary Center by Means of Chiral Phosphoric Acid: Highly Enantioselective Friedel-Crafts Reaction of Indoles with b,b-Disubstituted Nitroalkenes, Mori, K.; Wakazawa, M.; Akiyama, T. Chem. Sci.2014, 5, 1799–1803.
Double C(sp3)-H Bond Functionalization Mediated by Sequential Hydride Shift/Cyclization Process: Diastereoselective Construction of Polyheterocycles, Mori, K.; Kurihara, K.; Yabe, S.; Yamanaka, M.; Akiyama, T. J. Am. Chem. Soc.2014, 136, 3744–3747.
Expeditious Synthesis of 1-Aminoindane Derivatives Achieved by [1,4]-Hydride Shift Mediated C(sp3)-H Bond Functionalization, Mori, K.; Kurihara, K.; Akiyama, T. Chem. Commun.2014, 50, 3729–3731.
Enantioselective Fluorination of b-Ketoesters Catalyzed by Chiral Sodium Phosphate: Remarkable Enhancement of Reactivity by Simultaneous Utilization of Metal Enolate and Metal Phosphate, Mori, K.; Miyake, A.; Akiyama, T. Chem. Lett.2014, 43, 137–139.
Enantioselective Transfer Hydrogenation of Difluoromethyl Ketimines Using Benzothiazoline as a Hydrogen Donor in Combination with Chiral Phosphoric Acid, Sakamoto, T.; Horiguchi, K.; Saito, K.; Mori, K.; Akiyama, T. Asian. J. Org. Chem.2013, 2, 943–946.
Prediction of Suitable Catalyst by 1H NMR: Asymmetric Synthesis of Multisubstituted Biaryls by Chiral Phosphoric Acid Catalyzed Asymmetric Bromination, Mori, K.; Ichikawa, Y.; Kobayashi, M.; Shibata, Y.; Yamanaka, M.; Akiyama, T. Chem. Sci.2013, 4, 4235–4239.
Hydrodefluorinations of Trifluorotoluenes by LiAlH4 and TiCl4, Akiyama, T,; Atobe, K.; Shibata, M.; Mori, K.J. Fluorine. Chem.2013, 152, 81–83.
Enantioselective Synthesis of Multisubstituted Biaryl Skeleton by Chiral Phosphoric Acid Catalyzed Desymmetrization/Kinetic Resolution Sequence, Mori, K.; Ichikawa, Y.; Kobayashi, M.; Shibata, Y.; Yamanaka, M.; Akiyama, T. J. Am. Chem. Soc.2013, 135, 3964–3970 (Highlighted in Synfacts).
Kinetic Resolution in Chiral Phosphoric Acid Catalyzed Aldol Reactions: Enantioselective Robinson-Type Annulation Reactions, Yamanaka, M.; Hoshino, M.; Katoh, T.; Mori, K.; Akiyama, T. Eur. J. Org. Chem.2012, 4508–4514.
Chiral Phosphoric Acid Catalyzed Enantioselective Transfer Deuteration of Ketimines by Use of Benzothiazoline As a Deuterium Donor: Synthesis of Optically Active Deuterated Amines, Sakamoto, T.; Mori, K.; Akiyama, T. Org. Lett.2012, 14, 3312–3315.
Concise Route to 3-Arylisoquinoline Skeleton by Lewis Acid Catalyzed C(sp3)–H Bond Functionalization and Its Application to Formal Synthesis of (±)-Tetrahydropalmatine, Mori, K.; Kawasaki, T.; Akiyama, T. Org. Lett.2012, 14, 1436–1439.
Rapid Access to 3-Aryltetralin Skeleton via C(sp3)–H Bond Functionalization: Investigation on the Substituent Effect of Aromatic Ring Adjacent to C–H Bond in Hydride Shift/Cyclization Sequence, Mori, K.; Sueoka, S.; Akiyama, T. Chem. Lett.2011, 40, 1386–1388 (Selected as an Editor’s Choice paper).
Chiral Phosphoric Acid Catalyzed Transfer Hydrogenation: A Facile Synthetic Access to Highly Optically Active Trifluoromehylated Amines, Henseler, A.; Kato, M.; Mori, K.; Akiyama, T. Angew. Chem. Int. Ed.2011, 50, 8180–8183 (Highlighted in Synfacts).
Selective Activation of Enantiotopic C(sp3)–Hydrogen by Means of Chiral Phosphoric Acid: Asymmetric Synthesis of Tetrahydroquinoline Derivatives, Mori, K.; Ehara, K.; Kurihara, K.; Akiyama, T. J. Am. Chem. Soc.2011, 133, 6166–6169 (Highlighted in Synfacts).
Chiral Phosphoric Acid Catalyzed Enantioselective Synthesis of b-Amino-a,a-difluoro Carbonyl Compounds, Kashikura, W.; Mori, K.; Akiyama, T. Org. Lett.2011, 13, 1860–1863.
Expeditious Construction of a Carbobicyclic Skeleton via a sp3-C–H Functionalization: Hydride Shift from an Aliphatic Tertiary Position in an Internal Redox Process, Mori, K.; Sueoka, S.; Akiyama, T. J. Am. Chem. Soc.2011, 133, 2424–2426.
Chiral Br?nsted Acid-Catalyzed Asymmetric Friedel-Crafts Alkylation of Indoles with a,b-Unsaturated Ketones: Short Access to Optically Active 2- and 3-Substituted Indole Derivatives, Sakamoto, T.; Itoh, J.; Mori, K.; Akiyama, T. Org. Biomol. Chem.2010, 8, 5448–5454.
Niobium-catalyzed Activation of CF3 Group on Alkene: Synthesis of Substituted Indenes, Fuchibe, K.; Atobe, K.; Fujita, Y.; Mori, K.; Akiyama, T. Chem. Lett.2010, 39, 867–869.
Expeditious Synthesis of Benzopyrans via Lewis Acid-Catalyzed C–H Functionalization: Remarkable Enhancement of Reactivity by an Ortho Substituent, Mori, K.; Kawasaki, T.; Sueoka. S.; Akiyama, T. Org. Lett.2010, 12, 1732–1735.
Enantioselective Friedel-Crafts Alkylation of Indoles with Trifluoropyruvate Catalyzed by Chiral Phosphoric Acid, Kashikura, W.; Itoh, J.; Mori, K.; Akiyama, T. Chem. Asian J.2010, 5, 470–472.
Chiral Phosphoric Acid-Catalyzed Desymmetrization of meso-1,3-Diones: Asymmetric Synthesis of Chiral Cyclohexenones, Mori, K.; Katoh, T.; Suzuki, T.; Noji, T.; Yamanaka, M.; Akiyama, T. Angew. Chem. Int. Ed.2009, 48, 9652–9654 (Highlighted in Synfacts).
Expedient Synthesis of N-Fused Indoles: C–F Activation and C–H Insertion Approach, Fuchibe, K.; Kaneko, T.; Mori, K.; Akiyama, T. Angew. Chem. Int. Ed.2009, 48, 8070–8073 (VIP article).
Hydrogen-Bond Control in Axially Chiral Styrenes: Selective Synthesis of Enantiomerically Pure C2-Symmetric Paracyclophanes, Mori, K.; Ohmori, K.; Suzuki, K. Angew. Chem. Int. Ed.2009, 48, 5638–5641.
Stereochemical Relay via Axially Chiral Styrene: Asymmetric Synthesis of Antibiotic, TAN-1085, Mori, K.; Ohmori, K.; Suzuki, K. Angew. Chem. Int. Ed.2009, 48, 5633–5637 (Highlighted in Nature Chemistry).
Chiral Br?nsted Acid-Catalyzed Hydrophosphonylation of Imines: DFT Study on the Effect of Substituents of Phosphoric Acid, Akiyama, T.; Morita, H.; Bachu, P.; Mori, K.; Yamanaka, M.; Hirata, T. Tetrahedron2009, 65, 4950–4956.
Enantioselective Mannich-type Annulation Reaction Catalyzed by a Chiral Phosphoric Acid Bearing (S)-Biphenol Backbone, Akiyama, T.; Katoh, T.; Mori, K.; Kanno, K. Synlett2009, 1664–1666.
Dual Functionlization of Allene: Facile Construction of Heteropolycycles Mediated by Br?nsted Acid, Mori, K.; Sueoka, S.; Akiyama, T. Chem. Lett.2009, 38, 628–629.
Expeditious Construction of Quinazolines via Br?nsted Acid Induced C–H Activation: Further Extension of “tert-Amino Effect”, Mori, K.; Ohshima, Y.; Ehara, K.; Akiyama, T. Chem. Lett. 2009, 38, 524–525.
Enantioselective Aza-Darzens Reaction Catalyzed by A Chiral Phosphoric Acid, Akiyama, T.; Suzuki, T.; Mori, K.Org. Lett.2009, 11, 2445–2447.
