Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Takahiro Suto"'
Autor:
Takahiro Kawajiri, Akihito Kijima, Atsuhiro Iimuro, Eisaku Ohashi, Katsuya Yamakawa, Kazushi Agura, Kengo Masuda, Kensuke Kouki, Koji Kasamatsu, Shuichi Yanagisawa, Sho Nakashima, Setsuya Shibahara, Takashi Toyota, Takafumi Higuchi, Takahiro Suto, Tadashi Oohara, Toshikatsu Maki, Naoto Sahara, Nobuaki Fukui, Hisayuki Wakamori, Hidaka Ikemoto, Hiroaki Murakami, Hiroyasu Ando, Masahiro Hosoya, Mizuki Sato, Yusuke Suzuki, Yuta Nakagawa, Yuto Unoh, Yoichi Hirano, Yoshitomo Nagasawa, Satoshi Goda, Takafumi Ohara, Takayuki Tsuritani
Publikováno v:
ACS Central Science, Vol 9, Iss 4, Pp 836-843 (2023)
Externí odkaz:
https://doaj.org/article/9f38b46b1b194cdaac85377b26776798
Publikováno v:
Journal of Statistical Theory and Applications (JSTA), Vol 15, Iss 3 (2016)
For square contingency tables with ordered categories, the present paper proposes an asymmetry model with m-additional parameters, which indicates (1) the generalized marginal homogeneity and (2) the structure of quasi-symmetry for cumulative probabi
Externí odkaz:
https://doaj.org/article/dc65221d36d642b9b421fb1a20312506
Autor:
Yuto Unoh, Shota Uehara, Kenji Nakahara, Haruaki Nobori, Yukiko Yamatsu, Shiho Yamamoto, Yuki Maruyama, Yoshiyuki Taoda, Koji Kasamatsu, Takahiro Suto, Kensuke Kouki, Atsufumi Nakahashi, Sho Kawashima, Takao Sanaki, Shinsuke Toba, Kentaro Uemura, Tohru Mizutare, Shigeru Ando, Michihito Sasaki, Yasuko Orba, Hirofumi Sawa, Akihiko Sato, Takafumi Sato, Teruhisa Kato, Yuki Tachibana
Publikováno v:
Journal of Medicinal Chemistry. 65:6499-6512
The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in millions of deaths and threatens public health and safety. Despite the rapid global spread of COVID-19 vaccines,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda3f19d8c44fa9a7e86dcee58fa2330
https://doi.org/10.1021/acs.jmedchem.2c00117
https://doi.org/10.1021/acs.jmedchem.2c00117
Autor:
Takahiro Kawajiri, Akihito Kijima, Atsuhiro Iimuro, Eisaku Ohashi, Katsuya Yamakawa, Kazushi Agura, Kengo Masuda, Kensuke Kouki, Koji Kasamatsu, Shuichi Yanagisawa, Sho Nakashima, Setsuya Shibahara, Takashi Toyota, Takafumi Higuchi, Takahiro Suto, Tadashi Oohara, Toshikatsu Maki, Naoto Sahara, Nobuaki Fukui, Hisayuki Wakamori, Hidaka Ikemoto, Hiroaki Murakami, Hiroyasu Ando, Masahiro Hosoya, Mizuki Sato, Yusuke Suzuki, Yuta Nakagawa, Yuto Unoh, Yoichi Hirano, Yoshitomo Nagasawa, Satoshi Goda, Takafumi Ohara, Takayuki Tsuritani
We describe the development of the practical manufacturing of Ensitrelvir, which was discovered as a SARS-CoV-2 antiviral candidate. Scalable synthetic methods of indazole, 1,2,4-triazole and 1,3,5-triazinone structures were established, and converge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6fe8efc31eb0dbe319232ced6f96b7a
https://doi.org/10.26434/chemrxiv-2022-wx3nl
https://doi.org/10.26434/chemrxiv-2022-wx3nl
Publikováno v:
Asian Journal of Organic Chemistry. 10:2486-2502
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::092c8021c6ad84720baeba39ebfd1271
https://doi.org/10.1002/ajoc.202100421
https://doi.org/10.1002/ajoc.202100421
Autor:
Shinsaku Takikawa, Kazuki Miura, Yuta Yanagita, Takahiro Suto, Yoshiyuki Nagashima, Siro Simizu, Noritaka Chida, Takaaki Sato, Yasuhiro Kurosu, Naoya Matsuo
Publikováno v:
Bulletin of the Chemical Society of Japan. 92:545-571
The full details of a unified total synthesis of madangamine alkaloids are disclosed. Our central strategy is based on the construction of a common ABCE-tetracyclic system, followed by the late-sta...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40bf364965ba0e91d84bd6eb5d2814bf
https://doi.org/10.1246/bcsj.20180334
https://doi.org/10.1246/bcsj.20180334
Publikováno v:
Bioorganic & Medicinal Chemistry. 34:116041
Madangamines are marine natural products isolated from Xestospongia ingens, and madangamine A-E with a different D-ring structure have been reported. We have reported that madangamine A has strong anti-proliferative activity against various human can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce41d316610fd8dfac3c9b3c4768c6c8
https://doi.org/10.1016/j.bmc.2021.116041
https://doi.org/10.1016/j.bmc.2021.116041
Publikováno v:
Chemistry, an Asian journal. 13(8)
Full details of a stereodivergent hydroboration of allenes are reported. While hydroboration of an allene with 9-BBN provided a thermodynamically stable (E)-allylic alcohol after oxidative work-up, the reaction of an identical allene with HB(Sia)2 (d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce95b4e14255a397e1f932efcacde8b5
https://pubmed.ncbi.nlm.nih.gov/29431908
https://pubmed.ncbi.nlm.nih.gov/29431908
Publikováno v:
Organic Letters. 17:1946-1949
A general synthetic route toward a diazatricyclic core common to the madangamine family is described. Ring-closing metathesis and palladium-catalyzed cycloisomerization provided the cis-fused diazadecalin structure, accompanied by formation of the N-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a391e5ed109dbcefca3e7c0e6389bcf
https://doi.org/10.1021/acs.orglett.5b00661
https://doi.org/10.1021/acs.orglett.5b00661
Autor:
Noritaka Chida, Yasuhiro Kurosu, Shinsaku Takikawa, Takaaki Sato, Yoshiyuki Nagashima, Yuta Yanagita, Naoya Matsuo, Takahiro Suto
Publikováno v:
Journal of the American Chemical Society. 139(8)
A stereodivergent strategy for the synthesis of skipped dienes is developed. The method consists of hydroboration of allenes and Migita–Kosugi–Stille coupling, which allows for access to all four possible stereoisomers of the skipped dienes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e7185f672a36739ce415476147527c6
https://pubmed.ncbi.nlm.nih.gov/28190360
https://pubmed.ncbi.nlm.nih.gov/28190360