Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Takeshi Matsushita"'
Autor:
Masakazu Kondo, Takeshi Matsushita
Publikováno v:
ACS Omega, Vol 4, Iss 8, Pp 13426-13434 (2019)
Externí odkaz:
https://doaj.org/article/a7ac272f08184a278c7c349736d3550e
Autor:
Yusuke Sano, Toshiki Shintani, Masahiro Hayakawa, Susumu Oda, Masakazu Kondo, Takeshi Matsushita, Takuji Hatakeyama
Publikováno v:
Journal of the American Chemical Society. 145:11504-11511
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae31d2f91aed621f76508ff80a9c09ac
https://doi.org/10.1021/jacs.3c02873
https://doi.org/10.1021/jacs.3c02873
Autor:
Shiro Koseki, Masaki Yoshii, Toshio Asada, Yuichi Fujimura, Takeshi Matsushita, Shigeyuki Yagi
Publikováno v:
The Journal of Physical Chemistry A. 125:10604-10614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84619a2cd52847ed966f5c128df500b0
https://doi.org/10.1021/acs.jpca.1c08261
https://doi.org/10.1021/acs.jpca.1c08261
Autor:
Takamitsu Hosoya, Yuki Hazama, Suguru Yoshida, Yoshitake Nishiyama, Masakazu Kondo, Takeshi Matsushita, Sayuri Goto
Publikováno v:
Chemistry Letters. 48:1038-1041
The clickabilities of various alkenyl and alkyl azides in the strain-promoted cycloaddition with dibenzo-fused cyclooctynes were investigated. Although alkenyl azides generally exhibited lower clic...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a20c3af2b8aa31a284db6ac7c682c0b
https://doi.org/10.1246/cl.190400
https://doi.org/10.1246/cl.190400
Autor:
Yuji Ishii, Takeshi Matsushita, Hideyuki Yamada, Yukiko Hattori, Tomoki Takeda, Waka Izumoto, Misaki Fujii
Publikováno v:
Biochemical pharmacology. 178
A number of epidemiological studies have implicated environmental chemicals including dioxins in the induction of negative effects on child development. To clarify the underlying mechanisms, almost all toxicologists have concentrated on effects on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::909a66a21ba8bb82b632997ac64f0d6f
https://pubmed.ncbi.nlm.nih.gov/32569627
https://pubmed.ncbi.nlm.nih.gov/32569627
Autor:
Yun Yu, Yasuhiro Kondo, Huan Wang, Yutaka Matsuo, Toshiaki Ikuta, Takeshi Matsushita, Hiroshi Okada, Motoki Yanai, Il Jeon
Publikováno v:
ACS Applied Materials & Interfaces. 10:11810-11817
A diphenylanthracene dimethylamine derivative (9-{3,5-di(N,N-dimethylaminoethoxy)phenyl}-10-phenyl-anthracene, DPAMA) was synthesized by the Suzuki–Miyaura cross-coupling reaction. Its ammonium salt, 9-{3,5-di(trimethylammonium ethoxy)phenyl}-10-ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24501c8d71d11d614706500eb2df1d53
https://doi.org/10.1021/acsami.8b00603
https://doi.org/10.1021/acsami.8b00603
Autor:
Masanori Iwaki, Hidenori Miyata, Atsushi Naganawa, Akira Imagawa, Takuya Nishio, Jun Katagi, Yasuyuki Okabe, Takeshi Matsushita, Tatsuya Komagata, Akiharu Ishida, Toru Maruyama, Tetsuya Sekiguchi
Publikováno v:
Bioorganic & Medicinal Chemistry. 49:116424
Somatostatin receptors are members of G-protein coupled receptor superfamily. Receptors can be classified into five subtypes, SSTR1 to 5. The highly potent and orally active SSTR2 agonist 7, which had been identified by our group, was found out to ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4730bdf3d329b17feaea2d19b0e0ab
https://doi.org/10.1016/j.bmc.2021.116424
https://doi.org/10.1016/j.bmc.2021.116424
Autor:
Ryoji Shikata, Takeshi Matsushita, Chikahiko Mitsui, Masakazu Yamagishi, Katsumasa Nakahara, Akihito Yamano, Hiroyuki Ishii, Jun Takeya, Toshihiro Okamoto, Masafumi Yano, Hiroyasu Sato
Publikováno v:
Bulletin of the Chemical Society of Japan. 90:931-938
A series of oxygen- and sulfur-bridged bianthracene V-shaped π-electronic cores are facilely synthesized. We clarify their fundamental properties and aggregated structures in single crystals as well as measure their transistor performances in single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e897943c3cd08aacfed1cce02fc5b08
https://doi.org/10.1246/bcsj.20170030
https://doi.org/10.1246/bcsj.20170030
Autor:
Takamitsu Hosoya, Hana Nakajima, Keisuke Uchida, Takeshi Matsushita, Masakazu Kondo, Takahisa Yano, Suguru Yoshida
Publikováno v:
Chemistry Letters. 46:77-80
Reactions of arynes with sulfoximines are reported. The fate of these reactions depends on the substituents of the sulfoximines. S,S-Diarylsulfoximines reacted with arynes to selectively afford o-sulfinylanilines, whereas a simple N-arylation reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28b59f634d2ea779ab2499a53ed97af4
https://doi.org/10.1246/cl.160865
https://doi.org/10.1246/cl.160865
Autor:
Shiro Koseki, Masaki Yoshii, Toshio Asada, Yuichi Fujimura, Takeshi Matsushita, Shigeyuki Yagi
Publikováno v:
Journal of Physical Chemistry A; 12/23/2021, Vol. 125 Issue 50, p10604-10614, 11p