Laboratory of Chemical Bioscience

Institute of Biomaterials and Bioengineering

( IBB )

Tokyo Medical and Dental University

( TMDU )

Japanese / English


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“Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions”

S. Yoshida, K. Kanno, I. Kii, Y. Misawa, M. Hagiwara, and T. Hosoya*

Chem. Commun. 2018, 54, 3705.

Selected as inside back cover

“Staudinger reaction using 2,6-dichlorophenyl azide derivatives for robust aza-ylide formation applicable to bioconjugation in living cells”

T. Meguro, N. Terashima, H. Ito, Y. Koike, I. Kii, S. Yoshida,* and T. Hosoya*

Chem. Commun. 2018, 54, 7904.

Selected as back cover

“Expanding the synthesizable multisubstituted benzo[b]thiophenes via 6,7-thienobenzynes generated from o-silylaryl triflate-type precursors”

S. Yoshida,* T. Kuribara,  T. Morita,  T. Matsuzawa,  K. Morimoto,  T. Kobayashi, and T. Hosoya*

RSC Adv. 2018, 8, 21754.

“Transient Protection of Organic Azides from Click Reactions with Alkynes by Phosphazide Formation”

T. Meguro, S. Yoshida,* K. Igawa, K. Tomooka, and T. Hosoya*

Org. Lett. 2018, 20, 4126.

“Further enhancement of the clickability of doubly sterically-hindered aryl azides by para-amino substitution”

S. Yoshida,  J. Tanaka,  Y. Nishiyama, Y. Hazama, T. Matsushita, and  T. Hosoya*

Chem. Commun. 2018, 54, 13499–13502.

Selected as inside back cover

“Recent advances in reactions between arynes and organosulfur compounds”

T. Matsuzawa, S. Yoshida,* and  T. Hosoya*

Tetrahedron Lett. 2018, 59, 4197–4208.

“Synthesis of Diverse 3-Azido-5-(azidomethyl)benzene Derivatives via Formal C–H Azidation and Functional Group-Selective Transformations”

Y. Nishiyama, Y. Misawa, Y. Hazama, K. Oya, S. Yoshida,* and  T. Hosoya*

Heterocycles, in press.

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