Zobrazeno 1 - 10
of 184
pro vyhledávání: '"Tohru Oishi"'
Publikováno v:
Chemistry Letters; Sep2024, Vol. 53 Issue 9, p1-6, 6p
Autor:
Keitaro Umeno, Tohru Oishi
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 81:35-45
Autor:
Keitaro Umeno, Hisaaki Onoue, Keiichi Konoki, Kohei Torikai, Yoko Yasuno, Masayuki Satake, Tohru Oishi
Publikováno v:
Bulletin of the Chemical Society of Japan. 95:325-330
Autor:
Yuma Wakamiya, Tohru Oishi
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 79:664-672
Autor:
Michio Murata, Hiroshi Tsuchikawa, Shinya Hanashima, Tohru Oishi, Sangjae Seo, Tomoya Yamamoto, Kosuke Funahashi, Taiga Suzuki, Shigeru Matsuoka, Nobuaki Matsumori, Mayank Kumar Dixit, Yuichi Umegawa, Yasuo Nakagawa, Wataru Shinoda
Publikováno v:
Science Advances. 8
Amphotericin B, an antifungal drug with a long history of use, forms fungicidal ion-permeable channels across cell membranes. Using solid-state nuclear magnetic resonance spectroscopy and molecular dynamics simulations, we experimentally elucidated t
Autor:
Tohru Oishi
Publikováno v:
Bulletin of the Chemical Society of Japan. 93:1350-1360
Marine microorganisms are known to produce natural products, so called super carbon chain compounds whose molecular weights (MWs) exceed one thousand, such as amphidinol 3 (AM3) and maitotoxin (MTX...
Autor:
Tohru Oishi, Hiroshi Tsuchikawa
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 78:213-220
Autor:
Kohei Torikai, Yohei Joh, Tohru Oishi, Shamansur S. Sagdullaev, Khamid U. Khodjaniyazov, Milandip Karak
Publikováno v:
Synlett. 30:2058-2061
Addition of reactants under an inert atmosphere is a fundamental but extremely important technique in synthetic chemistry. Although this is achievable in many cases by using a glove box or a Schlenk-and-syringe technique, the direct addition of powde
Publikováno v:
Chemistry Letters. 48:1156-1159
Unified synthesis of 6/6/6-tricyclic ethers corresponding to the DEF and GHI ring systems of maitotoxin was achieved from a common intermediate prepared from a furan derivative and a terminal olefi...
Publikováno v:
Organic Letters. 21:1221-1225
The use of 2- O-alkoxymethyl groups as effective stereodirecting substituents for the construction of 1,2- trans glycosidic linkages is reported. The observed stereoselectivity arises from the intramolecular formation of a five-membered cyclic archit