Publication List (2016-2017)

Catalytic Carbon–Carbon Bond-Forming Reactions of Weakly Acidic Carbon Pronucleophiles Using Strong Brønsted Bases as Catalysts

Y. Yamashita, S. Kobayashi

Chem. Eur. J., 24, 10-17 (2018).DOI:10.1002/chem.201703404

Rhodium-catalyzed asymmetric 1,4-addition reactions of aryl boronic acids with nitroalkenes: reaction mechanism and development of homogeneous and heterogeneous catalysts

H. Miyamura, K. Nishino, T. Yasukawa, S. Kobayashi

Chem. Sci., 8 , 8362-8372 (2017). DOI: 10.1039/C7SC03025H

Water as a catalytic switch in the oxidation of aryl alcohols by polymer incarcerated rhodium nanoparticles

J. O. Weston, H. Miyamura, T. Yasukawa, D. Sutarma, C. A. Baker, P. K. Singh, M. Bravo-Sanchez, N. Sano, P. J. Cumpson, Y. Ryabenkova, S. Kobayashi, M. Conte

Catal. Sci. Technol. , 7, 3985-3998 (2017). DOI: 10.1039/C7CY01006K

Water-Compatible Chiral Lewis Acids

T. Kitanosono, S. Kobayashi

In Book Chiral Lewis Acids in Organic Synthesis, ed. by J. Mlynarski, Wiley-VCH , 299-344 (2017).

Catalytic Stereoselective 1,4-Addition Reactions Using CsF on Alumina as a Solid Base: Continuous-Flow Synthesis of Glutamic Acid Derivatives

P. Borah, Y. Yamashita, S. Kobayashi

Angew. Chem. Int. Ed., 56 , 10330-10334 (2017). DOI: 10.1002/anie.201701789

Copper-Catalyzed Enantioselective Boron Conjugate Addition: DFT and AFIR Study on Different Selectivities of Cu(I) and Cu(II) Catalysts

M. Isegawa, W. M. C. Sameera, A. K. Sharma, T. Kitanosono, M. Kato, S. Kobayashi, K. Morokuma

ACS Catal. , 7, 5370-5380 (2017). DOI: 10.1021/acscatal.7b01152

A polystyrene-supported phase-transter catalyst for asymmetric Michael addition of glycine-derived imines to α,β-unsaturated ketones

J. Miguelez, H. Miyamura, S. Kobayashi

Adv. Synth. Catal., 359 , 2897-2900 (2017). DOI: 10.1002/adsc.201700155

Incorporation of carbon dioxide into phthalides via ligand-free copper-catalyzed direct carboxylation of benzoxasiloles

T. V. Q. Nguyen, J. A. Rodriguez-Santamaria, W.-J. Yoo, S. Kobayashi

Green Chem. 19 , 2501-2505 (2017). DOI: 10.1039/C7GC00917H

Catalytic Direct-type 1,4-Addition Reactions of Alkylazaarenes

H. Suzuki, R. Igarashi, Y. Yamashita, S. Kobayashi

Angew. Chem. Int. Ed. 56 , 4520-4542 (2017) DOI: 10.1002/anie.201611374

Catalytic Asymmetric Direct-Type 1,4-Addition Reactions of Alkanesulfonamides

Y. Yamashita, R. Igarashi, H. Suzuki, S. Kobayashi

Synlett 11 , 1287-1290 (2017). DOI: 10.1055/s-0036-1588737

Selective Hydrogenation of Nitriles to Primary Amines Catalyzed by a Polysilane/SiO2-Supported Palladium Catalyst under Continuous-Flow Conditions

Y.Saito, H.Ishitani, M.Ueno and S.Kobayashi

Chem. Open. 6, 211-215 (2017).DOI: 10.1002/open.201600166

Lewis Acid-assisted Dirhodium(II)-catalyzed Ketone Hydroacylation

T. Yasukawa, S. Kobayashi

Chem. Lett. 46, 98-100 (2017). DOI: 10.1246/cl.160862

Integration of aerobic oxidation and intramolecular asymmetric aza-Friedel-Crafts reactions with a chiral bifunctional heterogeneous catalyst

H.-G. Cheng, J. Miguelez, H. Miyamura, W.-J. Yoo, S. Kobayashi

Chem. Sci., 8, 1356-1359 (2017). DOI: 10.1039/C6SC03849B

Lewis acid-driven reaction pathways in synergistic cooperative catalysis over gold%2Fpalladium bimetallic nanoparticles for hydrogen autotransfer reaction between amide and alcohol

H. Miyamura, S. Isshiki, H. Min, S. Kobayashi

Chinese J. Catal., 37, 1662-1668 (2016). DOI: 10.1016/S1872-2067(16)62483-X

Chiral Ligand-Modified Metal Nanoparticles as Unique Catalysts for Asymmetric CC Bond-Forming Reactions: How Are Active Species Generated?

T. Yasukawa, H. Miyamura and S. Kobayashi

ACS Catal. , 6, 7979-7988(2016). DOI: 10.1021/acscatal.6b02446

Catalytic Hydrogenation of Aliphatic Nitro Compounds with Polysilane/Bone Charcoal-Supported Palladium Catalysts under Continuous-Flow Conditions

Y. Saito, H. Ishitani, S. Kobayashi

Asian JOC , 5, 1124-1127 (2016). DOI: 10.1002/ajoc.201600279

Upregulation of an Artificial Zymogen by Proteolysis

Z. Liu, V. Lebrun, T. Kitanosono, H. Mallin, V. Köhler, D. Häussinger, D. Hilvert, S. Kobayashi, T. R. Ward

Angew. Chem. Int. Ed. , 55, 11587-11590 (2016). DOI: 10.1002/anie.201605010

Surfactant-aided chiral palladium(II) catalysis exerted exclusively in water for the C–H functionalization of indoles

T. Kitanosono, M. Miyo, S. Kobayashi

ACS Sustainable Chem. Eng. 4, 6101-6106(2016).DOI: 10.1021/acssuschemeng.6b01519

N-Heterocyclic Carbene Coordinated Heterogeneous Pd Nanoparticles as Catalysts for Suzuki–Miyaura Coupling

H. Min, H. Miyamura, S. Kobayashi

Chem. Lett.45, 837-839 (2016).DOI: 10.1246/cl.160369

Development of a Simple Adjustable Zinc Acid/Base Hybrid Catalyst for C-C and C-O Bond-Formation and C-C Bond-Cleavage Reactions

Y. Yamashita, K. Minami, Y. Saito, S. Kobayashi

Chem. Asian J.11, 2372-2376(2016).DOI: 10.1002/asia.201600682

Catalytic Asymmetric Direct-type 1,4-Addition Reactions of Simple Esters

I. Sato, H. Suzuki, Y. Yamashita, S. Kobayashi

Org. Chem. Front., 3, 1241-1245 (2016).DOI: 10.1039/C6QO00242K

Development of Chiral Metal Amides as Highly Reactive Catalysts for Asymmetric [3 + 2] Cycloadditions

Y. Yamashita, S. Yoshimoto, M. J. Dutton, S. Kobayashi

Beilstein J. Org. Chem., 12, 1447-1452 (2016). DOI: 10.3762/bjoc.12.140

Asymmetric Arylation of Imines Catalyzed by Heterogeneous Chiral Rhodium Nanoparticles

T. Yasukawa, T. Kuremoto, H. Miyamura, S. Kobayashi

Org. Lett.18, 2716-2718 (2016). DOI: 10.1021/acs.orglett.6b01172

Chiral Nanoparticles/Lewis Acids as Cooperative Catalysts for Asymmetric 1,4-Addition of Arylboronic Acids to α,β-Unsaturated Amides

T. Yasukawa, Y. Saito, H. Miyamura, S. Kobayashi

Angew. Chem., Int. Ed. Accepted DOI: 10.1002/anie.201601559

Enantioselective Organometallic Catalysis in Flow

H. Ishitani, Y. Saito, S. Kobayashi

Topics in Organometallic Chemistry , 57, 213-218 (2016). URL

Flow “Fine” Synthesis: High Yielding and Selective Organic Synthesis by Flow Methods

S. Kobayashi

Chem. Asian J., 11 , 425-426 (2016). DOI: 10.1002/asia.201500916

Synthesis of Nitro-Containing Compounds through Multistep Continuous Flow with Heterogeneous Catalysts

H. Ishitani, Y. Saito, T. Tsubogo, S. Kobayashi

Org. Lett., 18, 1346-1349 (2016). DOI: 10.1021/acs.orglett.6b00282

Chelating Bis(1,2,3-triazol-5-ylidene) Rhodium Complexes: Versatile Catalysts for Hydrosiylation Reactions

T. V. Q. Nguyen, W.-J. Yoo, S. Kobayashi

Adv. Synth. Catal. 358 , 452-458 (2016). DOI: 10.1002/adsc.201500875