Zobrazeno 1 - 10
of 456
pro vyhledávání: '"Hiroyuki, Koshino"'
Publikováno v:
ACS Omega, Vol 8, Iss 38, Pp 35382-35392 (2023)
Externí odkaz:
https://doaj.org/article/3ba3dbc64fe345a086c06ed2faf86325
Autor:
Go Hirai, Marie Kato, Hiroyuki Koshino, Eri Nishizawa, Kana Oonuma, Eisuke Ota, Toru Watanabe, Daisuke Hashizume, Yuki Tamura, Mitsuaki Okada, Taeko Miyagi, Mikiko Sodeoka
Publikováno v:
JACS Au, Vol 1, Iss 2, Pp 137-146 (2020)
Externí odkaz:
https://doaj.org/article/27cc34bd62c74af59d44d734c8c465da
Autor:
Hiroko Tani, Hiroyuki Koshino, Tohru Taniguchi, Maiko Yoshimatsu, Susumu Hikami, Shunya Takahashi
Publikováno v:
ACS Omega, Vol 5, Iss 21, Pp 12245-12250 (2020)
Externí odkaz:
https://doaj.org/article/7b9bebae0dd44bfe98702af7220e91d7
Autor:
Toshihiko Nogawa, Naoki Kato, Takeshi Shimizu, Akiko Okano, Yushi Futamura, Shunji Takahashi, Hiroyuki Koshino, Hiroyuki Osada
Publikováno v:
The Journal of Antibiotics. 76:346-350
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17b67ef62290077c35483461d8752c6
https://doi.org/10.1038/s41429-023-00613-2
https://doi.org/10.1038/s41429-023-00613-2
Publikováno v:
Bulletin of the Chemical Society of Japan. 96:318-320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14c03ac338794f6b4173b97160b694c4
https://doi.org/10.1246/bcsj.20230025
https://doi.org/10.1246/bcsj.20230025
Autor:
Nicolaus A. Herman, Seong Jong Kim, Jeffrey S. Li, Wenlong Cai, Hiroyuki Koshino, Wenjun Zhang
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-11 (2017)
Polyketides are secondary metabolites mainly found in aerobic organisms with wide applications in medicine and agriculture. Here, the authors uncover new polyketides native to the anaerobic bacterium Clostridium acetobutylicum and show their role in
Externí odkaz:
https://doaj.org/article/9b5f4f44dfc4465d8529d36c85ce5ad8
Autor:
Petr Funk, Kamil Motyka, Miroslav Soural, Michal Malon, Hiroyuki Koshino, Joachim Kusz, Jan Hlavac
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0175364 (2017)
2-Aminoquinolin-4(1H)-one was reacted with various primary/secondary amines and paraformaldehyde under Mannich reaction conditions. In the case of secondary amines, the reaction in N,N-dimethylformamide yielded expected Mannich products accompanied w
Externí odkaz:
https://doaj.org/article/e81ea93c0823426aae69db78cfd045ae
Autor:
Masaya Adachi, Hiroyuki Koshino, Mai Akakabe, Tetsuya Ezawa, Mikiko Sodeoka, Daisuke Hashizume, Yoshihiro Sohtome
Publikováno v:
Journal of the American Chemical Society. 143:9094-9104
Reaction design in asymmetric catalysis has traditionally been predicated on a structurally robust scaffold in both substrates and catalysts, to reduce the number of possible diastereomeric transition states. Herein, we present the stereochemical dyn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c1f674b52ad4b0bf39a7fa7192e8bb1
https://doi.org/10.1021/jacs.1c02833
https://doi.org/10.1021/jacs.1c02833
Autor:
Ryo Fukazawa, Kana Oonuma, Risa Maeda, Keiya Uezono, Marie Kato, Hiroyuki Koshino, Masaki Morita, Taeko Miyagi, Mikiko Sodeoka, Go Hirai
We designed α(2,3)- and α(2,6)-sialylgalactose analogues bearing an exomethylene unit at C3 of sialic acid (3-exoSia) as a novel type of mechanism-based inhibitors of sialidases. Regio- and stereo-selective substitution by vinylogous activation ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b03f1358b6b844243cfb2c8264a90f6
https://doi.org/10.26434/chemrxiv-2022-vd8cr
https://doi.org/10.26434/chemrxiv-2022-vd8cr
Autor:
Hiroyuki Osada, Katsuyuki Sakai, Risa Takao, Hiroyuki Koshino, Yushi Futamura, Shunji Takahashi
Publikováno v:
The Journal of Antibiotics. 74:593-595
A novel angucyclinone, 6,9-dihydroxytetrangulol, was isolated from Streptomyces lividans TK23 transformed with a kinanthraquinone biosynthetic gene cluster in which the kiqO gene was disrupted. The chemical structure was elucidated by spectroscopic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131503a34694199844c581a6ededaac1
https://doi.org/10.1038/s41429-021-00442-1
https://doi.org/10.1038/s41429-021-00442-1