Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tomoteru MIZUSAKI"'
Autor:
Yuta Yamamoto, Eisho Shimizu, Kazuho Ban, Yoshiyuki Wada, Tomoteru Mizusaki, Masatoshi Yoshimura, Yukio Takagi, Yoshinari Sawama, Hironao Sajiki
Publikováno v:
ACS Omega, Vol 5, Iss 6, Pp 2699-2709 (2020)
Externí odkaz:
https://doaj.org/article/2a6557b508d742b98e4d03bf27af43e8
Autor:
Momo YAMANE, Yuto SEO, Wahyu S. PUTRO, Miftah FARIED, Vladimir Ya. LEE, Tomoteru MIZUSAKI, Yukio TAKAGI, Kazuhiro MATSUMOTO, Jun-Chul CHOI, Norihisa FUKAYA
Publikováno v:
Journal of the Japan Petroleum Institute. 66:23-26
Autor:
Tomoteru MIZUSAKI
Publikováno v:
Journal of the Japan Petroleum Institute. 66:1-7
Autor:
Eisho Shimizu, Wada Yoshiyuki, Yoshinari Sawama, Tomoteru Mizusaki, Yuta Yamamoto, Hironao Sajiki, Masatoshi Yoshimura, Kazuho Ban, Yukio Takagi
Publikováno v:
ACS Omega, Vol 5, Iss 6, Pp 2699-2709 (2020)
ACS Omega
ACS Omega
The palladium-on-carbon (Pd/C)-catalyzed hydrogenative deprotection of the N-benzyl-protecting group was effectively facilitated by the combined use of niobic acid-on-carbon (Nb2O5/C). Nb2O5/C is an acidic heterogeneous catalyst prepared from NbCl5 a
Autor:
Norihisa Fukaya, Jun-Chul Choi, Tomoteru Mizusaki, Katsuhiko Takeuchi, Yukio Takagi, Kazuhiro Matsumoto
Publikováno v:
Organometallics. 38:1872-1876
An immobilized N-heterocyclic carbene (NHC)-Pd complex was prepared via direct silyl linker installation onto the imidazole backbone of commercially available 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr) ligand. The IPr backbone was lithiat
Autor:
Tomoteru Mizusaki, Yoong-Kee Choe, Norihisa Fukaya, Jun-Chul Choi, Junpei Kuwabara, Kouhei Hatakeyama, Yukio Takagi, Yuto Seo, Yuuya Inaba, Kazuhiro Matsumoto, Vladimir Ya. Lee, Takaki Kanbara
Publikováno v:
Organometallics. 38:375-384
A family of Pd–IPr complexes (1Pd–6Pd) featuring electropositive and bulky R3Si substituents at the 4-position of the NHC ring was prepared and fully characterized. The catalytic performance of 1Pd (R3Si = SiMe3) and 3Pd (R3Si = Si(allyl)Me2) in
Autor:
Tomoteru Mizusaki, Jun-Chul Choi, Yoong-Kee Choe, Wahyu S. Putro, Miftah Faried, Yukio Takagi, Vladimir Ya. Lee, Norihisa Fukaya, Kazuhiro Matsumoto, Yuto Seo
Publikováno v:
Journal of Organometallic Chemistry. :122096
A series of R3Si-NHC-Pd complexes 1Pd-7Pd was successfully tested as a pre-catalyst for the Suzuki-Miyaura cross-coupling reaction of aryl chlorides and arylboronic acid derivatives to form a wide range of valuable biphenyl products. Use of the readi
Autor:
Tomoteru Mizusaki, Hironao Sajiki, Yasunari Monguchi, Tomohiro Ichikawa, Masahiro Mizuno, Yukio Takagi, Moeko Netsu, Yoshinari Sawama
Publikováno v:
Advanced Synthesis & Catalysis. 359:2269-2279
A unique heterogeneous palladium catalyst (7% Pd/WA30) supported on an anion exchange resin, which contains N,N-dimethylaminoalkyl functionalities on the polymer backbone, was developed. 7% Pd/WA30 could smoothly catalyze Suzuki–Miyaura reaction of
Autor:
Tomoteru Mizusaki, Hironao Sajiki, Tomohiro Hattori, Tomohiro Ichikawa, Yasunari Monguchi, Moeko Netsu, Yoshinari Sawama
Publikováno v:
Synlett. 26:2014-2018
A palladium catalyst supported on a tertiary-amino-functionalized resin bearing N,N-dimethylamino substituents on the polystyrene-divinylbenzene-based resin was developed. The catalyst was effectively used for the ligand-free Suzuki–Miyaura reactio
Autor:
Yasunari Monguchi, Tomohiro Ichikawa, Yoshinari Sawama, Moeko Netsu, Tomohiro Hattori, Tomoteru Mizusaki, Hironao Sajiki
Publikováno v:
ChemInform. 47
A palladium catalyst supported on a tertiary-amino-functionalized resin bearing N,N-dimethylamino substituents on the polystyrene-divinylbenzene-based resin was developed. The catalyst was effectively used for the ligand-free Suzuki–Miyaura reactio