Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Yohei Ogiwara"'
Autor:
Yohei Ogiwara, Kotohiro Nomura
Publikováno v:
ACS Organic & Inorganic Au, Vol 3, Iss 6, Pp 377-383 (2023)
Externí odkaz:
https://doaj.org/article/5829cf577647425e940b70df0f2da345
Publikováno v:
Molecules, Vol 23, Iss 6, p 1339 (2018)
An indium-catalyzed reaction of lactones and a disilathiane leading to thiolactones is described. The direct synthesis of thiolactones from lactones with an appropriate sulfur source is one of the most attractive approaches in organic and pharmaceuti
Externí odkaz:
https://doaj.org/article/e9560acacec5432692fd542447abe140
Publikováno v:
Synthesis. 55:1915-1921
Described herein is an iodide-promoted insertion reaction of vinyltrimethylsilane into diaryl or dialkyl disulfides in the presence of iodine/KF leading to the production of a 1,1′-adduct, a dithioacetal derivative. This method also accomplishes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc0ca675ee6de71a15b4871ade6bf3aa
https://doi.org/10.1055/a-2014-3203
https://doi.org/10.1055/a-2014-3203
Publikováno v:
Synthesis. 55:779-785
A copper-catalyzed construction of isothiochromenes and benzo[b]thiophenes via annulation with 1,1,1,3,3,3-hexamethyldisilathiane as a sulfur source is described. In the isothiochromene synthesis, the use of the disilathiane as a sulfur source succes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6affc76f53014c66294f8f89b79fc5b6
https://doi.org/10.1055/a-1953-4534
https://doi.org/10.1055/a-1953-4534
Publikováno v:
Organometallics. 41:1509-1518
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc77cb7d1c116a8c04186697cf89feff
https://doi.org/10.1021/acs.organomet.2c00165
https://doi.org/10.1021/acs.organomet.2c00165
Publikováno v:
Synthesis. 54:2661-2668
We have developed a two-step synthesis of dibenzotetrathiafulvalene (DBTTF) derivatives by combining the indium-catalyzed reductive dithioacetalization of oxalic acid and electron-rich aromatic dithiols with a subsequent oxidation of the resultant di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64da0d81ec75fa8840ae711be90d55da
https://doi.org/10.1055/a-1742-2821
https://doi.org/10.1055/a-1742-2821
Publikováno v:
Chemistry – An Asian Journal. 16:4103-4107
The results of this study show that disilathiane is an effective mediator in the synthesis of alkyl aryl sulfides with disulfides and alkyl carboxylates. Mechanistic studies suggest that disilathiane promotes cleavage of the sulfur-sulfur bond of dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb249203c0b89adc33d75364d7fed664
https://doi.org/10.1002/asia.202101101
https://doi.org/10.1002/asia.202101101
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e439e6de711f49b7fece4ae39d9d5a3d
https://doi.org/10.1002/ejoc.202201407
https://doi.org/10.1002/ejoc.202201407
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c18ebb3fd975128c8cd9e02f6e7d7349
https://doi.org/10.1002/ejoc.202201118
https://doi.org/10.1002/ejoc.202201118
Publikováno v:
Bulletin of the Chemical Society of Japan. 94:1882-1893
The catalytic intramolecular cyclization of acyl fluorides using a Pd(OAc)2/PCy3 system is described. A wide range of 2-arylbenzoyl fluoride derivatives can be used as fluorenone precursors and the...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86cad9644c1765b8ee343a965e48c717
https://doi.org/10.1246/bcsj.20210148
https://doi.org/10.1246/bcsj.20210148