Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Toshifumi, Kuribayashi"'
Autor:
Takuya, Murai, Yongning, Xing, Mayu, Kurokawa, Toshifumi, Kuribayashi, Masanori, Nikaido, Elghareeb E, Elboray, Shohei, Hamada, Yusuke, Kobayashi, Takahiro, Sasamori, Takeo, Kawabata, Takumi, Furuta
Publikováno v:
The Journal of organic chemistry. 87(9)
A one-pot transformation of biaryl dicarboxylic acids to (
Autor:
Takuya Murai, Norihiro Tokitoh, Wenjie Lu, Yusuke Kobayashi, Yoshihiro Ueda, Toshifumi Kuribayashi, Takahiro Sasamori, Kazuhiro Morisaki, Shohei Hamada, Takeo Kawabata, Takumi Furuta
Publikováno v:
ACS Catalysis. 11:568-578
D2-symmetric dirhodium(II) carboxylate catalysts that bear axially chiral binaphthothiophene δ-amino acid derivatives have been developed. Conformational control is supported through chalcogen-bond...
Autor:
Yongning Xing, Yusuke Kobayashi, Masanori Nikaido, Takeo Kawabata, Takuya Murai, Toshifumi Kuribayashi, Shohei Hamada, Mayu Kurokawa, Elghareeb E. Elboray, Takumi Furuta, Takahiro Sasamori
A one-pot transformation of biaryl dicarboxylic acids to (NH)-phenanthridinone derivatives based on a Curtius rearrangement and subsequent basic hydrolysis was developed. This method is also applicable for the preparation of optically active amide-fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afaa0f3e18316b40224f141137ed27bf
https://doi.org/10.26434/chemrxiv-2021-0wzfl
https://doi.org/10.26434/chemrxiv-2021-0wzfl
Autor:
Takahiro Sasamori, Lu W, Yoshihiro Ueda, N. Tokitoh, Kazuhiro Morisaki, Takuya Murai, Takeo Kawabata, Toshifumi Kuribayashi, Shohei Hamada, Takumi Furuta
Novel well-defined D2-symmetric dirhodium(II) carboxylate complexes that bear axially chiral binaphthothiophene delta-amino acid derivatives have been developed. Conformational control was achieved through chalcogen-bonding interactions between sulfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02ff4c97ba2abcfb29033e14c6b3991d
https://doi.org/10.26434/chemrxiv.12547262.v1
https://doi.org/10.26434/chemrxiv.12547262.v1
Autor:
Takeo Kawabata, Norihiro Tokitoh, Ramesh Yella, Yongning Xing, Toshifumi Kuribayashi, Jing-Dong Guo, Takumi Furuta, Shohei Hamada, Takahiro Sasamori, Takuya Murai, Wenjie Lu
Publikováno v:
Chemicalpharmaceutical bulletin. 66(12)
Axially chiral binaphthothiophene dicarboxylic acid was prepared as a novel functionalized chiral dicarboxylic acid. The crystal structures of both the racemic form and its salt with chiral diamine revealed the intramolecular S···O interactions (c
Publikováno v:
Synthesis. 45:1312-1318
Axially chiral amino acid derivatives were synthesized via a selective single-step monoesterification of 1,1′-binaphthyl-2,2′-dicarboxylic acids. In the presence of Ag2CO3, the alkylative monoesterification of a 1,1′-binaphthyl-2,2′-dicarboxy
Autor:
Yoshiji Takemoto, Toshifumi Kuribayashi, Taro Enomoto, Shota Sakamoto, Shinsuke Yokouchi, Chihiro Tsukano, Anne-Lise Girard
Publikováno v:
ChemInform. 44
The Pt-catalyzed cyclization of various internal alkynylamides provides access towards diazepines with excellent 7-endo selectivity.
Autor:
Chihiro Tsukano, Shota Sakamoto, Shinsuke Yokouchi, Yoshiji Takemoto, Toshifumi Kuribayashi, Taro Enomoto, Anne-Lise Girard
Publikováno v:
Organicbiomolecular chemistry. 10(30)
The scope and limitations of the platinum catalyzed 7-endo cyclization of internal alkynyl amides were investigated. Substitution of the alkyne with an aryl group gave better results, presumably because it stabilized the transition state. Applying th