Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Miyuki Yamaguchi"'
Publikováno v:
Frontiers in Fungal Biology, Vol 3 (2022)
The biogenesis of small non-coding RNAs is a molecular event that contributes to cellular functions. The basidiomycete fungus Ustilago maydis is a biotrophic pathogen parasitizing maize. A hallmark of its genome structure is an absence of RNAi machin
Externí odkaz:
https://doaj.org/article/be5ef003b93a45be8a3d870784f01e35
Autor:
Miyuki Yamaguchi
Publikováno v:
EXARC Journal, Iss 2021/3 (2021)
“Cooperating to create a greater impact" was a session during the ICOM General Conference in Kyoto, Japan. It was organized by ICOM NL, ICOM JP, DEMHIST, EXARC and the Japan Museum Sieboldhuis. The session took place on September 4, 2019 at Kyoto I
Externí odkaz:
https://doaj.org/article/97efe59cee764e7792674cd46908e0ec
Publikováno v:
Molecules, Vol 18, Iss 12, Pp 15207-15219 (2013)
A repetitive two-step method involving the Pd-catalyzed Suzuki-Miyaura coupling of hydroxyterphenylboronic acid and the subsequent nonaflation of the hydroxy group has been developed for the synthesis of oligophenylenes. This method readily afforded
Externí odkaz:
https://doaj.org/article/7386b96f4ef442619b83847cfb2b6181
Publikováno v:
Organic Letters. 24:3663-3667
Herein, we present a safe and practical methodology for synthesizing symmetrical sulfides using iodoarenes and potassium metabisulfite (K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::721c454f5cd2686f2fa3603777e3af63
https://doi.org/10.1021/acs.orglett.2c01284
https://doi.org/10.1021/acs.orglett.2c01284
Autor:
Yusuke Sato, Miyuki Yamaguchi, Kei Manabe, Kanami Gayama, Hideyuki Konishi, Kohei Suzuki, Ryoya Hagiwara
Publikováno v:
The Journal of Organic Chemistry. 85:10902-10912
A palladium-dihydroxyterphenylphosphine (DHTP) catalyst was successfully applied to the direct C3-arylation of N-unsubstituted indoles with aryl chlorides, triflates, and nonaflates. This catalyst showed C3-selectivity, whereas catalysts with other s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c80dae8db08a1a5b9624a58546cd329d
https://doi.org/10.1021/acs.joc.0c01494
https://doi.org/10.1021/acs.joc.0c01494
Publikováno v:
Tetrahedron. 123:132962
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06a99cd2185761a88e10e6e7ab4b267e
https://doi.org/10.1016/j.tet.2022.132962
https://doi.org/10.1016/j.tet.2022.132962
Publikováno v:
Organic Letters. 21:6972-6977
Palladium-catalyzed site-selective dearomative C2-arylation of 2,5-diaryl-1H-pyrroles with aryl chlorides was accomplished, and a series of 2,2,5-triaryl-2H-pyrroles were synthesized. In addition, the site selectivity of the reaction was switched by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd15064e7b4da2d1f2e896b63ab9dc8c
https://doi.org/10.1021/acs.orglett.9b02559
https://doi.org/10.1021/acs.orglett.9b02559
Autor:
Miyuki Yamaguchi, James E. Haber
Publikováno v:
Homologous Recombination ISBN: 9781071606438
Methods Mol Biol
Methods Mol Biol
By using an inducible site-specific double-strand break (DSB) in budding yeast, it is possible to monitor-in real time-the repair of the break by homologous recombination. A method is described using an ectopic homologous donor sequence to repair an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75bbb2ceb9acaf17493f695c0bfa1af8
https://doi.org/10.1007/978-1-0716-0644-5_16
https://doi.org/10.1007/978-1-0716-0644-5_16
Autor:
Kei Manabe, Miyuki Yamaguchi
Publikováno v:
HETEROCYCLES. 104:3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2209730a18e86e07bcb32b625509285
https://doi.org/10.3987/rev-21-964
https://doi.org/10.3987/rev-21-964
Publikováno v:
Tetrahedron Letters. 59:3175-3178
2,3-Disubstituted benzofurans possessing 2-hydroxyphenyl moiety at the C-3 position were synthesized from readily available 2-chlorophenols and terminal alkynes by hydroxy-directed ortho-Sonogashira coupling and subsequent oxypalladation/reductive el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0e7b9fca06bf67363f70bc093a9bfe6
https://doi.org/10.1016/j.tetlet.2018.07.019
https://doi.org/10.1016/j.tetlet.2018.07.019