Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Naoya OHTSUKA"'
Autor:
Shunya Oishi, Takeshi Fujinami, Yu Masui, Toshiyasu Suzuki, Masayuki Kato, Naoya Ohtsuka, Norie Momiyama
Publikováno v:
STAR Protocols, Vol 4, Iss 1, Pp 102140- (2023)
Summary: In this protocol, we describe the application of a halogen(I) complex as a highly active non-metallic complex catalyst. Specifically, we present a detailed guide to synthesize the halogen(I) complex catalyst and utilize it as an anion-bindin
Externí odkaz:
https://doaj.org/article/1a4fa46351314457834f75873fc79c78
Autor:
Shunya Oishi, Takeshi Fujinami, Yu Masui, Toshiyasu Suzuki, Masayuki Kato, Naoya Ohtsuka, Norie Momiyama
Publikováno v:
iScience, Vol 25, Iss 10, Pp 105220- (2022)
Summary: The three-center-four-electron halogen bond (3c4e X-bond) presents a fundamental design concept for catalysis. By integrating halogen(I) (X+: I+ or Br+), the bis-pyridyl ligand NN, and a non-nucleophilic counteranion Y, we developed non-meta
Externí odkaz:
https://doaj.org/article/7726a3fde36f489281de5746e11e8268
Autor:
Methanee Hiranyakorn, Maho Yagi-Utsumi, Saeko Yanaka, Naoya Ohtsuka, Norie Momiyama, Tadashi Satoh, Koichi Kato
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6075 (2023)
In multidomain proteins, individual domains connected by flexible linkers are dynamically rearranged upon ligand binding and sensing changes in environmental factors, such as pH and temperature. Here, we characterize dynamic domain rearrangements of
Externí odkaz:
https://doaj.org/article/cabb94035c534076b84bc3e79776707c
Autor:
Norie Momiyama, Chanantida Jongwohan, Naoya Ohtsuka, Pawittra Chaibuth, Takeshi Fujinami, Kiyohiro Adachi, Toshiyasu Suzuki
Publikováno v:
The Journal of Organic Chemistry. 87:9399-9407
A catalytic asymmetric methylene migration reaction of ene-aldimines directed by chiral counteranions is developed, with the optimal catalyst identified as phenanthryl-substituted (
Autor:
Tatsuaki HORI, Shuya KAKINUMA, Naoya OHTSUKA, Takeshi FUJINAMI, Toshiyasu SUZUKI, Norie MOMIYAMA
The Wittig reaction of perfluorohalobenzaldehydes was systematically studied to investigate perfluorohalostyrenes (TFXS) as functional monomers of halogen bond-driven smart polymer materials. The reaction proceeded efficiently in THF using 1,1,3,3-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::585effb14e741d094a550430f85c3fee
https://doi.org/10.26434/chemrxiv-2023-lcf1g
https://doi.org/10.26434/chemrxiv-2023-lcf1g
Autor:
Masayuki KATO, Fumio NAKASHIMA, Naoya OHTSUKA, Yukina NISHIOKA, Atsuto IZUMISEKI, Takeshi FUJINAMI, Shunya OISHI, Toshiyasu SUZUKI, Norie MOMIYAMA
Linker structures were systematically investigated for use in designing halogen-bond donor catalysts with two-point activation modes based on perfluoroiodobenzenes. Tetrafluorophenylene, phenylene, and acetylene were examined as potential linkers, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef984cf98efb9ece03324fbb8e93380d
https://doi.org/10.26434/chemrxiv-2023-sq0fl
https://doi.org/10.26434/chemrxiv-2023-sq0fl
Autor:
Atsuto Izumiseki, Naoya Ohtsuka, Tomoyuki Koganezawa, Ryohei Tsuruta, Norie Momiyama, Yuki Nakanishi, Kana Takahashi, Kazuhiko Mase, Masahiro Hiramoto, Yuki Gunjo, Riku Takeuchi, Yasuo Nakayama, Seiichiro Izawa
Publikováno v:
The Journal of Physical Chemistry Letters
Single-crystalline organic semiconductors exhibiting band transport have opened new possibilities for the utilization of efficient charge carrier conduction in organic electronic devices. The epitaxial growth of molecular materials is a promising rou
Autor:
Shunya Oishi, Takeshi Fujinami, Yu Masui, Toshiyasu Suzuki, Masayuki Kato, Naoya Ohtsuka, Norie MOMIYAMA
The three-center-four-electron halogen bond (3c4e X-bond) presents a new design concept for catalysis. By integrating halogen(I) (X+: I+ or Br+), bis-pyridyl ligand NN, and non-nucleophilic counter anion Y, we developed non-metallic complex catalysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7fda7911cfda71a481bdddce3434f68
https://doi.org/10.21203/rs.3.rs-1511322/v1
https://doi.org/10.21203/rs.3.rs-1511322/v1
Autor:
Shunya OISHI, Takeshi FUJINAMI, Yu MASUI, Toshiyasu SUZUKI, Masayuki KATO, Naoya OHTSUKA, Norie MOMIYAMA
The three-center-four-electron halogen bond (3c4e X-bond) presents a new design concept for catalysis. By integrating halogen(I) (X+: I+ or Br+), bis-pyridyl ligand NN, and non-nucleophilic counter anion Y. [N···X···N]SbF6, we developed non-met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71d6c1250e2f5cf3340199623d347f89
https://doi.org/10.26434/chemrxiv-2022-1ljk9
https://doi.org/10.26434/chemrxiv-2022-1ljk9
Autor:
Ko Ueno, Kiyoshi Honda, Naoya Ohtsuka, Kenta Tanaka, Yuta Tanaka, Shuto Sunaga, Yosuke Asada, Mami Kishimoto, Yujiro Hoshino
Publikováno v:
Synlett. 31:1197-1200
An inverse-electron-demand [4+2] cycloaddition of in situ generated aliphatic vinyl ethers and electron-deficient ortho-quinone methides (o-QMs) has been developed. The reaction of in situ generated aliphatic vinyl ethers with o-QMs afforded the corr