Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mamiko Hayakawa"'
A simple and efficient procedure for the synthesis of N-substituted acryl amides has been developed using Na2CO3/SiO2 or NaHSO4/SiO2. Na2CO3/SiO2 smoothly acts as a base in the reaction between acryloyl chloride and a variety of amines to obtain thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9afd0592312ea446898d09d29f2b5d96
Publikováno v:
ARKIVOC: Online Journal of Organic Chemistry. 2021, Vol. 2021, p145-154. 10p.
A Facile Approach to the Synthesis of 3-Acylisoxazole Derivatives with Reusable Solid Acid Catalysts
Publikováno v:
Synthesis. 53:4636-4643
Nitrile oxides were formed from α-nitro ketones using silica gel-supported sodium hydrogen sulfate (NaHSO4/SiO2) or Amberlyst 15 as solid acid catalyst, and then the corresponding 3-acylisoxaszoles were obtained by reacting with alkynes via the 1,3-
Publikováno v:
Arkivoc. 2021:145-154
Publikováno v:
Arkivoc. 2020:81-93
Publikováno v:
Tetrahedron Letters. 60:1493-1497
A simple and efficient method was developed for the synthesis of 1,4-thiazin-2-one O-(tert-butyl) oximes and benzo[b][1,4]thiazin-2-one O-(tert-butyl) oximes from N-tert-butoxy acyl imidoyl bromides and 2-aminothiols in the presence of K2CO3/SiO2. Tw
Publikováno v:
Synthesis. 51:2572-2578
A four-step synthesis of benzo- and naphthothiophenes that have biological importance and application in material science was integrated into a one-pot reaction by using silica gel-supported acid and base reagents, NaHSO4/SiO2 and Na2CO3/SiO2. The su
Autor:
Tadashi Aoyama, Akihiko Ouchi, Mamiko Hayakawa, Ken-ichi Itoh, Takuya Hanzawa, Natsumi Meguro, Miki Osanai
Publikováno v:
European Journal of Organic Chemistry. 2018:6363-6368
Publikováno v:
Tetrahedron Letters. 59:4116-4119
A simple and efficient method was developed for the synthesis of 5,6-dihydropyrazin-2(1H)-one O-(tert-butyl)oximes, quinoxalin-2(1H)-one O-(tert-butyl)oximes and its derivatives from N-tert-butoxy acyl imidoyl bromide and diamines. Twenty three novel
Sunlight-induced C C bond formation reaction: Radical addition of alcohols/ethers/acetals to olefins
Autor:
Mamiko Hayakawa, Hisashi Shirota, Ryuusei Yamada, Souta Hirayama, Akihiko Ouchi, Tadashi Aoyama
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 413:113263
A sunlight-induced C C bond formation reactions upon the addition of alcohols/ethers/acetals to olefins proceeded efficiently using di-tert-butyl peroxide (DTBP). The reactions proceeded faster than many of the previously reported sunlight and many c