Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Motohiro Sonoda"'
Publikováno v:
SynOpen, Vol 04, Iss 04, Pp 99-106 (2020)
Facile, iodine-mediated access to N-aryl-2-benzoxazolamines has been achieved in a one-pot manner under mild reaction conditions. Reaction of 2-aminophenols and aryl isothiocyanates afforded N-aryl-2-benzoxazolamines in the presence of molecular iodi
Externí odkaz:
https://doaj.org/article/961bfeeb28c74b5ca5c50a5a5597001c
Autor:
Shintaro Kodama, Vu Thai Hung, Tomokazu Saeki, Kei Mihara, Yuki Yamamoto, Motohiro Sonoda, Akihiro Nomoto, Akiya Ogawa
Publikováno v:
Molbank, Vol 2021, Iss 4, p M1283 (2021)
2,2-Bis(phenylselanyl)-1-(p-tolyl)vinyl 2-oxo-2-(p-tolyl)acetate was synthesized via the reaction of p-tolylacetylene with diphenyl diselenide and benzoyl peroxide in benzene under atmospheric conditions. The molecular structure of the synthesized co
Externí odkaz:
https://doaj.org/article/c2b78087712743d9b3ee5e5c97b492d4
Publikováno v:
Results in Chemistry, Vol 3, Iss , Pp 100252- (2021)
5-Hydroxyequol, a biologically active isoflavone metabolite from genistein, has been synthesized enantioselectively from 3-(2,4,6-trimethoxyphenyl)propanal by using MacMillans’ asymmetric α -arylation protocol of carbonyl compound. (S)- and (R)-5-
Externí odkaz:
https://doaj.org/article/b20805afb0e248c1ad06a0ee75183be5
Autor:
Mia Imanishi, Motohiro Sonoda, Hironari Miyazato, Keiichiro Sugimoto, Mitsugu Akagawa, Shinji Tanimori
Publikováno v:
ACS Omega, Vol 2, Iss 5, Pp 1875-1885 (2017)
Externí odkaz:
https://doaj.org/article/e0f03689c06041519d7158a576803b99
Autor:
Shin-ichi Kawaguchi, Yuhei Gonda, Takuya Yamamoto, Yuki Sato, Hiroyuki Shinohara, Yohsuke Kobiki, Atsuhiko Ichimura, Takashi Dan, Motohiro Sonoda, Toshio Miyata, Akiya Ogawa, Tadayuki Tsujita
Publikováno v:
Molecules, Vol 23, Iss 4, p 885 (2018)
Induction of a series of anti-hypoxic proteins protects cells during exposure to hypoxic conditions. Hypoxia-inducible factor-α (HIF-α) is a major transcription factor that orchestrates this protective effect. To activate HIF exogenously, without e
Externí odkaz:
https://doaj.org/article/57c2d53b449348bb8febbd147cb03896
Publikováno v:
The Journal of Organic Chemistry. 86:17727-17737
A new method to synthesize γ-carboline derivatives has been developed starting from 3,5-dibromo-4-pyridinamine by monoarylation using the Suzuki-Miyaura cross-coupling reaction followed by the base-mediated ring closure to pyrrole formation. Synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f4160c68014af69924af1caa9b76a2c
https://doi.org/10.1021/acs.joc.1c02026
https://doi.org/10.1021/acs.joc.1c02026
Autor:
Haruna Nariki, Kouhei Makiyama, Motohiro Sonoda, Asuka Fuchiya, Shizuki Noda, Takuya Miyamura, Shinji Tanimori
Publikováno v:
Synthesis. 54:483-489
A facile and environmentally benign access to N-aryl/alkyl-4H-benzoxazin-2-amines is achieved from 1-[2-(hydroxymethyl)phenyl/alkyl]-3-phenylthioureas under transition-metal-free conditions. The conversions occur smoothly in the presence of a catalyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80c8815d2a88349f4693c1c3e3ef6c2c
https://doi.org/10.1055/s-0040-1719832
https://doi.org/10.1055/s-0040-1719832
Aromatic carbonyl thiourea PI-28 has been focused on as a lead compound for the developing radicle elongation inhibitors in germinating Orobanche minor dry seeds. In this study, we have synthesized PI-28 and its derivatives using commercially availab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b9fd17eae6d42f76277cdda36b49f40
https://doi.org/10.26434/chemrxiv-2022-7qm8l
https://doi.org/10.26434/chemrxiv-2022-7qm8l
Publikováno v:
ChemistrySelect. 6:1533-1540
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b236e8ac87f19dce516032d823f2e8a4
https://doi.org/10.1002/slct.202100069
https://doi.org/10.1002/slct.202100069
Publikováno v:
Synlett. 32:693-696
Equol, a nonsteroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzein, has been synthesized as both enantioenriched forms based on MacMillan’s α-arylation of carbonyl compound mediated by amino acid derived indazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51b99e05471089cd19888f3ea82785c3
https://doi.org/10.1055/a-1303-9935
https://doi.org/10.1055/a-1303-9935