Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Kaname Shibata"'
Autor:
Taichi Ogawa, Junji Shibasaki, Atsushi Morinaga, Kaname Shibata, Akitsugu Suzuki, Yamato Takeuchi, Shoya Satake, Takuya Asada, Tomohiro Itagaki, Masahiro Fujiwara, Ikuya Shibata, Norihide Enomoto
Publikováno v:
Results in Materials, Vol 24, Iss , Pp 100630- (2024)
The serious problems of skin inflammations (dermatitides) observed in the users of rubber gloves caused by type I or type IV hypersensitivity strongly require their new manufacturing methods free from these irritations. This paper reports our novel a
Externí odkaz:
https://doaj.org/article/06fc8189f181472e804b2988805f3041
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Investigating unusual organometallic pathways may help to efficiently control product selectivity in homogeneous catalysis. Here, the authors report the hydroarylation of aromatic amides with norbornene derivatives and propose the formation of a rhod
Externí odkaz:
https://doaj.org/article/fe975581af0e40b3840956db9500644a
Autor:
Naoto Chatani, Kaname Shibata
Publikováno v:
Chemical Science. 7:240-245
An unprecedented C–H alkylation using α,β-unsaturated γ-lactones (butenolides) and dihydrofurans was achieved by the Rh-catalyzed reaction of benzamides. C–C bond formation occurs between the ortho-position of the benzamide derivative and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5219c4b9e2cfa00f801aae3e154336f5
https://doi.org/10.1039/c5sc03110a
https://doi.org/10.1039/c5sc03110a
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Hydroarylation is an environmentally attractive strategy which incorporates all of the atoms contained in the substrates into the desired products. Almost all the hydroarylations of norbornene reported to date involve an exo-selective reaction. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9df317594aa10122a5b92ca78beb7cd
https://pubmed.ncbi.nlm.nih.gov/29129930
https://pubmed.ncbi.nlm.nih.gov/29129930
Publikováno v:
Organic letters. 19(9)
The rhodium-catalyzed alkenylation of C–H bonds of aromatic amides with alkynes is reported. A variety of functional groups, including OMe, OAc, Br, Cl, and even NO2, are applicable to this reaction to give the corresponding hydroarylation products
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3570e7ccdb61828db726291843a65434
https://pubmed.ncbi.nlm.nih.gov/28430449
https://pubmed.ncbi.nlm.nih.gov/28430449
Publikováno v:
Chemistry Letters. 44:621-623
The reaction of arylacetamides that contain a quinolin-8-ylmethylamine as the directing group with PhI(OAc)2, in the presence of Pd(OAc)2 as the catalyst, results in lactonization to give γ-lactone...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a24ca39932af108c77c64b6f096703b
https://doi.org/10.1246/cl.150041
https://doi.org/10.1246/cl.150041
Autor:
Satoshi Inoue, Naoto Chatani, Yoshiya Fukumoto, Kaname Shibata, Nao Hasegawa, Valentine Charra
Publikováno v:
Tetrahedron. 69:4466-4472
The regioselective carbonylation of unactivated C(sp3)–H bonds of aliphatic amides, using 2-pyridinylmethylamine as a directing group in conjunction with Ru3(CO)12 as a catalyst is described. The presence of a 2-pyridinylmethylamine moiety in the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb3f90d53a674a93edc161df28c16f6e
https://doi.org/10.1016/j.tet.2013.02.006
https://doi.org/10.1016/j.tet.2013.02.006
Autor:
Naoto Chatani, Kaname Shibata
Publikováno v:
ChemInform. 47
An unprecedented C–H alkylation using α,β-unsaturated γ-lactones (butenolides) and dihydrofurans was achieved by the Rh-catalyzed reaction of benzamides. C–C bond formation occurs between the ortho-position of the benzamide derivative and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14dd9fe66a5744993723e1567c805690
https://doi.org/10.1002/chin.201618108
https://doi.org/10.1002/chin.201618108
Publikováno v:
ChemCatChem. 4:1733-1736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49880f1c0f4bb9767e8d1d69df6305bc
https://doi.org/10.1002/cctc.201200352
https://doi.org/10.1002/cctc.201200352
Publikováno v:
Cement Science and Concrete Technology. 64:435-441
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f6322e4d09e194bd18a5f6bb183752c
https://doi.org/10.14250/cement.64.435
https://doi.org/10.14250/cement.64.435