Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hayato Shirakura"'
Autor:
Hayato Shirakura1, Yuh Hijikata2 hijikata@icredd.hokudai.ac.jp, Pirillo, Jenny2, Tomoki Yoneda1, Yumehiro Manabe1,2, Murugavel, Muthuchamy, Yuki Ide2 ide.yuki@icredd.hokudai.ac.jp, Yasuhide Inokuma1,2 inokuma@eng.hokudai.ac.jp
Publikováno v:
European Journal of Inorganic Chemistry. 5/7/2021, Vol. 2021 Issue 17, p1705-1708. 4p.
Autor:
Yuki Ide, Hayato Shirakura, Taichi Sano, Muthuchamy Murugavel, Yuya Inaba, Sheng Hu, Ichigaku Takigawa, Yasuhide Inokuma
Visual observations are frequently used as a preliminary evaluation of the chemical contents of mixtures, but their accuracy largely depends on the observer’s experience and intuition, which are difficult to share. Here, we report component ratio p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a35524c271247d3f25eb98a6dbe5f7b
https://doi.org/10.26434/chemrxiv-2023-3gdsb
https://doi.org/10.26434/chemrxiv-2023-3gdsb
Autor:
Yasuchika Hasegawa, Yuichi Kitagawa, Tomoki Yoneda, Yuki Ide, Makoto Tsurui, Yuya Inaba, Hayato Shirakura, Yasuhide Inokuma, Yumehiro Manabe, Chika Kasai
Publikováno v:
European Journal of Organic Chemistry. 2021:4345-4349
Autor:
Tomoki Yoneda, Muthuchamy Murugavel, Yumehiro Manabe, Hayato Shirakura, Yuh Hijikata, Yasuhide Inokuma, Jenny Pirillo, Yuki Ide
Publikováno v:
European Journal of Inorganic Chemistry. 2021:1705-1708
Publikováno v:
Organicbiomolecular chemistry. 18(17)
Oligoacetylacetones consisting of 3,3-disubstituted pentane-2,4-diones were synthesized through a terminal silylation and oxidative coupling protocol. Highly selective formation of mono-enol silyl ethers of 3,3-disubstituted acetylacetones was achiev
Publikováno v:
Organic & Biomolecular Chemistry; 5/7/2020, Vol. 18 Issue 17, p3195-3202, 8p
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Publikováno v:
Organic & Biomolecular Chemistry; 5/7/2020, Vol. 18 Issue 17, p3297-3302, 6p