Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Fumitoshi Shibahara"'
Autor:
Takuya Sonoda, Masaya Kanamori, Koki Endo, Kazuki Miwa, Satoshi Kurumada, Katsunori Suzuki, Makoto Yamashita, Fumitoshi Shibahara
Publikováno v:
Israel Journal of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59a11b35ed32fee1cfee2e6c93bdc81e
https://doi.org/10.1002/ijch.202200038
https://doi.org/10.1002/ijch.202200038
Publikováno v:
Asian Journal of Organic Chemistry. 7:1323-1326
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74444111c362ba4fb0c257aed38e9318
https://doi.org/10.1002/ajoc.201800160
https://doi.org/10.1002/ajoc.201800160
Publikováno v:
Organic & Biomolecular Chemistry. 15:1810-1820
Various 1-substituted-imidazo[1,5-a]pyridin-3-ylidenes were prepared and characterized. The fundamental character and the effects of substituents on the imidazo[1,5-a]pyridine backbone on the electronic character of carbenes were evaluated using rhod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c62a5e8b16e6c1d573fac91ae98eb202
https://doi.org/10.1039/c6ob02827f
https://doi.org/10.1039/c6ob02827f
Autor:
Yasuhiro Kawai, Fumitoshi Shibahara, Shigesaki Kaga, Toshiaki Murai, Kimitaka Futamura, Ryuta Wada
Publikováno v:
Tetrahedron. 83:131978
A new route to thiophene-ring-fused compounds with thionyl chloride as a sulfur source was developed. Use of an excess amount thionyl chloride directly gave the corresponding thiophene-ring-fused compound via further reduction of generated thiophene-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ae031973ff24a6a2af5c2a8b0aca253
https://doi.org/10.1016/j.tet.2021.131978
https://doi.org/10.1016/j.tet.2021.131978
Publikováno v:
Tetrahedron Letters. 57:2945-2948
The arylative cyclization of o -(1-alkynyl)thioanisoles with aryl iodides in the presence of catalytic amounts of [Pd(phen) 2 ][PF 6 ] 2 resulted in the efficient formation of 3-arylated benzo[ b ]thiophenes, and a range of aryl iodides with electron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4cfafdc45c332ebe1e17e20034b3dbc
https://doi.org/10.1016/j.tetlet.2016.05.033
https://doi.org/10.1016/j.tetlet.2016.05.033
Autor:
Toshifumi Maruyama, Fumitoshi Shibahara, Hiroaki Kubuki, Tomohiko Mizutani, Akihito Yoshida, Kirara Yamaguchi, Toshiaki Murai
Publikováno v:
Chemistry Letters. 46:1017-1019
The reactions of 2-pyrones and coumarins with hydrochlorosilane, elemental selenium, and 4-dimethylaminopyridine (DMAP) gave 2-selenopyrones and selenocoumarins in moderate to good yields. Their fo...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0989eb3c6765a3d3286ce89d93f9387f
https://doi.org/10.1246/cl.170341
https://doi.org/10.1246/cl.170341
Publikováno v:
Organic letters. 20(18)
A synthetic route to chiral selenazolines from readily available N-acyloxazolidinones via a selenative rearrangement of a chiral cyclic skeleton is reported. The reaction proceeds in the presence of elemental selenium, a hydrochlorosilane, and an ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e6428834d8dfa39e0badde9bdd02c68
https://pubmed.ncbi.nlm.nih.gov/30179009
https://pubmed.ncbi.nlm.nih.gov/30179009
Autor:
Taro Udagawa, Toshiaki Murai, Fumitoshi Shibahara, Saki Kubota, Masafumi Suzuki, Tomoki Fukunaga
Publikováno v:
The Journal of organic chemistry. 83(6)
A highly diastereoselective α-allylation of selenolactams with allyl halides is reported. DFT analyses and experimental observations suggested that this reaction proceeds via a Se-allylation of the eneselenolates of the lactams followed by a seleno-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6c068e1f30a10e618511c62dd5a7392
https://pubmed.ncbi.nlm.nih.gov/29494158
https://pubmed.ncbi.nlm.nih.gov/29494158
Publikováno v:
Organic Letters. 17:5392-5395
A direct C-H bond arylation method for thienyl thioamides catalyzed by [Pd(phen)2](PF6)2 was developed. This reaction selectively afforded 2-monoarylated products, while the corresponding amide thiophene derivatives furnished 2,5-diarylated products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ae54ac9bb10a4b7f37dcff6ee924f81
https://doi.org/10.1021/acs.orglett.5b02742
https://doi.org/10.1021/acs.orglett.5b02742
Publikováno v:
Journal of Organometallic Chemistry. 794:76-80
Rh(I) and Ir(I) complexes bearing imidazo[1,5-a]pyridine-1-ylalkyl alcohol as chelating NˆO-monoanionic ligands were prepared as thermally stable compounds. Their spectroscopic properties and structures were determined based on IR and NMR spectra an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d87de69e4f2f8d93a84d7687c61eabd1
https://doi.org/10.1016/j.jorganchem.2015.05.045
https://doi.org/10.1016/j.jorganchem.2015.05.045