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pro vyhledávání: '"Yukino Shinomoto"'
Autor:
Yukino Shinomoto, Naoki Asari, Viktor V. Zhdankin, Takuma Yagyu, Akio Saito, Akira Yoshimura, Yusuke Takemoto
Publikováno v:
Asian Journal of Organic Chemistry. 5:1314-1317
As a first example for metal-free and catalytic fluorinative transformations of alkynes, we developed a cycloisomerization-fluorination sequence of N-propargyl amides catalyzed by iodine(III) species. The iodine(III) catalyst is in situ generated fro
Autor:
Viktor V. Zhdankin, Mutsumi Yamazaki, Akio Saito, Hisato Shimizu, Akira Yoshimura, Yukino Shinomoto
Publikováno v:
ChemInform. 47
The process succeeds using various aryl and alkyl aldehydes, and the products are isolated in moderate yields as the corresponding methyl carbamates obtained via Curtius-rearrangement.
Autor:
Yukino Shinomoto, Akira Yoshimura, Hisato Shimizu, Mutsumi Yamazaki, Viktor V. Zhdankin, Akio Saito
Publikováno v:
Organic letters. 17(21)
Tetra-n-butylammonium iodide can efficiently catalyze direct azidation of aldehyde C–H bonds with thermally stable azidobenziodoxolone at room temperature. Compared to conventional methods, which require excessive amounts of highly explosive azide
Autor:
Takuma Yagyu, Akio Saito, Yukino Shinomoto, Naoki Asari, Yusuke Takemoto, Viktor V. Zhdankin, Akira Yoshimura
Publikováno v:
Asian Journal of Organic Chemistry. 5:1295-1295
Autor:
Yukino Shinomoto, Akira Yoshimura, Hisato Shimizu, Mutsumi Yamazaki, ViktorV. Zhdankin, Akio Saito
Publikováno v:
Organic Letters; Nov2015, Vol. 17 Issue 21, p5212-5215, 4p