原著論文 | Original Papers

N-Heterocyclic Carbene-Catalyzed Truce–Smiles Rearrangement of N-Arylacrylamides via the Cleavage of Unactivated C(aryl)–N Bonds
K. Yasui, M. Kamitani, H. Fujimoto, M. Tobisu
Org. Lett. ASAP.
DOI: 10.1021/acs.orglett.0c04281

The Effect of the Leaving Group in N-Heterocyclic Carbene-Catalyzed Nucleophilic Aromatic Substitution Reactions
K. Yasui, M. Kamitani, H. Fujimoto, M. Tobisu
Bull. Chem. Soc. Jpn. 2020, 93, 1424–1429.
DOI: 10.1002/anie.201907837

N-Heterocyclic Carbene Catalyzed Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing α,β‐Unsaturated Amides
K. Yasui, M. Kamitani, M. Tobisu
Angew. Chem. Int. Ed. 2019, 58, 14157–14161.
DOI: 10.1002/anie.201907837

Nickel-Catalyzed Decarboxylation of Aryl Carbamates for Converting Phenols into Aromatic Amines
A. Nishizawa, T. Takahira, K. Yasui, H. Fujimoto, T. Iwai, M. Sawamura, N. Chatani, M. Tobisu
J. Am. Chem. Soc. 2019, 141, 7261–7265.
DOI: 10.1021/jacs.9b02751

11-Step Total Synthesis of Teleocidins B-1–B-4
H. Nakamura, K. Yasui, Y. Kanda, P. S. Baran
J. Am. Chem. Soc. 2019, 141, 1494–1497.
DOI: 10.1021/jacs.8b13697

Rhodium-Catalyzed C–O Bond Alkynylation of Aryl Carbamates with Propargyl Alcohols
K. Yasui, N. Chatani, M. Tobisu
Org. Lett. 2018, 20, 2108–2111.
DOI: 10.1021/acs.orglett.8b00674

C−O Activation by a Rhodium Bis(N-Heterocyclic Carbene) Catalyst: Aryl Carbamates as Arylating Reagents in Directed C−H Arylation
M. Tobisu, K. Yasui, Y. Aihara, N. Chatani
Angew. Chem. Int. Ed. 2017, 56, 1877–1880.
DOI: 10.1002/anie.201610409

Rhodium-Catalyzed Reductive Cleavage of Aryl Carbamates Using Isopropanol as a Reductant
K. Yasui, M. Higashino, N. Chatani, M. Tobisu
Synlett 2017, 28, 2569–2572.
DOI: 10.1055/s-0036-1589093

Rhodium-catalyzed cross-coupling of aryl carbamates with arylboron reagents
K. Nakamura, K. Yasui, M. Tobisu, N. Chatani
Tetrahedron 2015, 71, 4484–4489.
DOI: 10.1016/j.tet.2015.02.088