Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Akihiro Ogura"'
Autor:
Taishu Yoshinaga, Momoka Shinoda, Yoshiki Iso, Tetsuhiko Isobe, Akihiro Ogura, Ken-ichi Takao
Publikováno v:
ACS Omega, Vol 6, Iss 2, Pp 1741-1750 (2021)
Externí odkaz:
https://doaj.org/article/4528edff72a749b89b4f346324951de9
Autor:
Yukino Ochi, Ayano Otani, Rika Katakami, Akihiro Ogura, Ken-ichi Takao, Yoshiki Iso, Tetsuhiko Isobe
Publikováno v:
Journal of Materials Chemistry C; 5/14/2024, Vol. 12 Issue 18, p6548-6558, 11p
Publikováno v:
Journal of Materials Chemistry C. 11:4143-4152
DAR-derived carbon quantum dots (CQDs) in ethanol exhibited narrow-bandwidth red photoluminescence that was comparable to that of blue-fluorescent PG-derived-CQDs.
Publikováno v:
The Journal of Organic Chemistry. 87:8788-8795
Autor:
Akihiro Ogura
Publikováno v:
World Journal of Mechanics. 12:51-56
Publikováno v:
The Journal of Organic Chemistry. 86:10067-10087
A diaryliodonium salt-based strategy enabled the first systematic synthesis of rarely accessible N-alkoxyindolines. Mechanistic analyses suggested that the reaction likely involves reductive elimination of iodobenzene from iodaoxazepine via a four-me
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 78:1039-1047
Publikováno v:
Bulletin of the Chemical Society of Japan. 93:936-941
A red-light-mediated Barton–McCombie reaction is described, in which chlorophyll a is used as a photocatalyst and tris(trimethylsilyl)silane or Hantzsch ester is used as the hydrogen source. The re...
Publikováno v:
Synlett. 31:421-433
In this Account, we describe our studies on the total synthesis of several natural products using intramolecular Nozaki–Hiyama–Takai–Kishi (NHTK) reactions. In each synthesis, an NHTK reaction is used to efficiently construct a medium-sized rin
Autor:
Akihiro Ogura, Akihiro Sakama, Keisuke Yoshida, Ken Ichi Takao, Wataru Sumida, Yuta Unno, Yuko Motohashi, Rika Kameshima
Publikováno v:
The Journal of Organic Chemistry. 85:3245-3264
Two stereocontrolled routes to the tricyclic core of (-)-callophycoic acid A are described. Our synthetic strategy relied on stereoselective allylboration using a new allylboronate reagent to construct the all-carbon quaternary stereocenter in the co