Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Ryo, Takayama"'
Autor:
Takanori Uchida, Teppei Tanaka, Ryuta Shizui, Hiroto Ichikawa, Ryo Takayama, Kazuomi Yahagi, Ryoya Okubo
Publikováno v:
Wind Engineering. 47(2):408-421
To verify the effectiveness of the GPU simulation of wake effects at a large-scale offshore wind farm, we ran an in-house large-eddy simulation (LES) solver with a CFD porous disk wake model for the Horns Rev 1 wind farm. For this numerical research,
Publikováno v:
ARKIVOC, Vol 2018, Iss 2, Pp 72-80 (2017)
Externí odkaz:
https://doaj.org/article/d40335202d82458181bc727670d45f50
Publikováno v:
Chemistry – A European Journal.
Autor:
Takeshi Tsumuraya, Daisuke Fujiwara, Kousuke Mihara, Ryo Takayama, Yusuke Nakamura, Ikuo Fujii, Mitsuhiro Ueda
Publikováno v:
ChemBioChem. 22:3406-3409
Conformationally constrained peptides hold promise as molecular tools in chemical biology and as a new modality in drug discovery. The construction and screening of a target-focused library could be a promising approach for the generation of de novo
Publikováno v:
Bulletin of the Chemical Society of Japan. 94:2451-2465
The synthesis of 1,1-difluoro-1-alkenes was achieved by the treatment of dithioesters and thioketones with trimethylsilyl 2-fluorosulfonyl-2,2-difluoroacetate in the presence of a proton sponge cat...
Publikováno v:
Angewandte Chemie (International Ed. in English)
A novel catalyst‐free approach to benzoannulated oxygen‐containing heterocycles from fluorinated oligophenylenes is reported. Unlike existing methods, the presented reaction does not require an oxygen‐containing precursor and relies on an exter
Autor:
Kohei Fuchibe, Ibuki Mukohara, Atsushi Yamada, Daisuke Miyazaki, Ryo Takayama, Junji Ichikawa
Publikováno v:
Organic letters. 24(1)
The reaction of aryl thiophene-2-carbodithioates or thiophene-3-carbodithioates with difluorocarbene generated from BrCF
Publikováno v:
The Journal of organic chemistry. 86(21)
Herein, we report a facile transition-metal-free approach to sulfur-containing heteroacenes from fluorinated oligophenylenes. Unlike most existing methods, the presented approach is not restricted to simple dibenzothiophene derivatives and thus appea
Publikováno v:
Organicbiomolecular chemistry. 19(33)
Herein, we describe a facile synthesis of N-arylated carbazoles via ladderization of fluorinated oligophenylenes. The reaction consists of two subsequent nucleophilic substitutions triggered by an electronic transfer from dimsyl anions. The reaction
Autor:
Masayuki Nihei, Marina Kato, Haruki Murakami, Yoshihiro Sekine, Ryo Takayama, Karin Shiroyanagi, Hiroki Oshio, Yosuke Kera
Publikováno v:
Inorganic Chemistry. 58:11912-11919
Discrete cyanide-bridged Co–Fe multinuclear complexes can be considered as functional units of bulk Co–Fe Prussian blue analogues, and they have been recognized as a new class of switching molecule...