Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Shuhei Higashibayashi"'
Autor:
Masamichi Yasui, Takashi Fujihara, Hiroyoshi Ohtsu, Yuki Wada, Terumasa Shimada, Yiying Zhu, Masaki Kawano, Kengo Hanaya, Takeshi Sugai, Shuhei Higashibayashi
Publikováno v:
Communications Chemistry, Vol 6, Iss 1, Pp 1-6 (2023)
Abstract Photophysical properties of benzil (1,2-diphenylethane-1,2-dione) and its derivatives in the crystal state have recently attracted much attention. However, the study of substituted benzils has mostly been limited to para-substituted derivati
Externí odkaz:
https://doaj.org/article/68e4e2d50e9d447bbb8d591b578dd4bd
Publikováno v:
Communications Chemistry, Vol 6, Iss 1, Pp 1-10 (2023)
Abstract The biomimetic two-phase strategy employing polyene cyclization and subsequent oxidation/substitution is an effective approach for divergent syntheses of [6-6-6]-tricyclic diterpenes. However, this strategy requires lengthy sequences for syn
Externí odkaz:
https://doaj.org/article/326dbfb932bc408e809e925eddd4bb50
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-5 (2021)
Abstract Construction of the hydroquinoline skeleton of symbioimine by Cu-mediated N-alkenylation or O-alkenylation of an allyl aminoalcohol, in which either chemoselectivity could lead to the target compound, was investigated. O-alkenylation followe
Externí odkaz:
https://doaj.org/article/411f177d8aed46f49f2708daa8348f3c
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-6 (2018)
Abstract Hydrazine-embedded heterocyclic compounds with dimeric dimethylacridine (1b), carbazole (2b), and phenothiazine (3b) skeletons were applied to cathode active materials of rechargeable lithium organic batteries, and the performance of the bat
Externí odkaz:
https://doaj.org/article/730494160a804b14b69429f49a836938
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 841-847 (2014)
A single crystal of pyrenylsumanene was found to exhibit both columnar and herringbone crystal packing. The sumanene moieties form unidirectional columnar structures based on π–π stacking while the pyrene moieties generate herringbone structures
Externí odkaz:
https://doaj.org/article/be304f4b35554c7b91c16dbd16555b7c
Autor:
Masataka Nakahara, Yuki Wada, Masaki Kawano, Kengo Hanaya, Takeshi Sugai, Shuhei Higashibayashi
Publikováno v:
Chemistry Letters; May2024, Vol. 53 Issue 5, p1-4, 4p
Autor:
Kaho Harada, Chika Hasegawa, Taisuke Matsumoto, Hiroki Sugishita, Chitoshi Kitamura, Shuhei Higashibayashi, Masashi Hasegawa, Shuichi Suzuki, Shin-ichiro Kato
Publikováno v:
Chemical Communications. 59:1301-1304
The title compound has a sufficiently persistent radical cationic state and enough chiral stability for optical resolution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::348ca1dda5e96d04ebe9275feee1cd71
https://doi.org/10.1039/d2cc06144a
https://doi.org/10.1039/d2cc06144a
Publikováno v:
Chemical Communications. 59:748-751
A cyclization of m-homoprenylphenols through an oxidative nucleophilic aromatic substitution using the prenyl group as a carbon nucleophile was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e297fdccdedb5a57317ebbd13b6a5fc5
https://doi.org/10.1039/d2cc06026d
https://doi.org/10.1039/d2cc06026d
Autor:
Go Hirai, Makoto Yoritate, Hiroki Yasutomi, Daiki Takeda, Shuhei Higashibayashi, Takeshi Sugai
Publikováno v:
Synlett. 34:347-352
C-Glycoside analogues of native glycans are useful molecular tools for medicinal chemistry and chemical biology due to their resistance to cellular glycoside hydrolases. We previously reported an α-selective direct C-glycosylation of 2-deoxy-β-glyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b4d8fdc58527ed3ca51e53fa2e3d663
https://doi.org/10.1055/a-1989-2541
https://doi.org/10.1055/a-1989-2541
Publikováno v:
Organic Letters. 24:5596-5601
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9206af8044d8c132ab83543750024f58
https://doi.org/10.1021/acs.orglett.2c02305
https://doi.org/10.1021/acs.orglett.2c02305