Organic Chemistry for Life Science
Developing new methodologies for the construction of a broad range of molecules significant in life sciences
Acylalkylation of Arynes Generated from o-Iodoaryl Triflates with Hydrosilanes and Cesium Fluoride
M. Minoshima, K. Uchida, Y. Nakamura, T. Hosoya,
Org. Lett. 2021, 23, 1868.
Diverse diaryl sulfide synthesis through consecutive aryne reactions
H. Nakajima, Y. Hazama, Y. Sakata, K. Uchida, T. Hosoya, *S. Yoshida
Chem. Commun., 2021, 57, 2621.
Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations
*S. Yoshida, Y. Sakata, Y. Misawa, T. Morita, T. Kuribara, H. Ito, Y. Koike, I. Kii, *T. Hosoya
Chem. Commun., 2021, 57, 899.
Facile Synthesis of Tetraarylpyrazines by Sequential Cross-coupling Approach
Y. Nishiyama, K. Akiyama, Y. Sakata, T. Hosoya, *S. Yoshida
Chem. Lett. 2021, 50, 180.
Selected as Editor’s choice; Open Access
Transition-Metal-Free Synthesis of N-Arylphenothiazines through an N- and S-Arylation Sequence
T. Matsuzawa, T. Hosoya, *S. Yoshida
Org. Lett. 2021, 23, 2347.
Sequential conjugation methods based on triazole formation and related reactions using azides
Org. Biomol. Chem. 2020, 18, 1550.
Invited Review; Open Access
Recent review article
Recent original papers
Department of Biological Science and Technology
Palladium-Catalyzed Sulfinylation of Aryl- and Alkenylborons with Sulfinate Esters
M. Suzuki, K. Kanemoto, Y. Nakamura, T. Hosoya,
Org. Lett. 2021, in press.