Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yuki Egoshi"'
Autor:
Akane Yamagishi, Yuki Egoshi, Makoto T. Fujiwara, Noriyuki Suzuki, Tohru Taniguchi, Ryuuichi D. Itoh, Yumiko Suzuki, Yoshiro Masuyama, Kenji Monde, Toyonobu Usuki
Publikováno v:
Chemistry – A European Journal. 29
Foeniculoxin is a major phytotoxin produced by Italian strains of Phomopsis foeniculi. The first total synthesis is described utilizing the ene reaction and Sonogashira cross-coupling reaction as key steps. The absolute configuration of the C6' was d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a3af7e1ac2aac6d9b3579b61823ed22
https://doi.org/10.1002/chem.202203396
https://doi.org/10.1002/chem.202203396
Autor:
Takaya Mori, Yumiko Suzuki, Tomoya Uchiyama, Yukiko Yoshimoto, Noriyuki Suzuki, Dinda B. Pitna, Yuki Egoshi, Shoya Yamaguchi, Tenma Nakamura, Ryosuke Kondo, Shihori Hara, Kogaku Kimura, Toyonobu Usuki
Publikováno v:
Organic & Biomolecular Chemistry. 19:6038-6044
Cynaropicrin is found in artichoke (Cynara scolymus) and is the source of its bitter taste and it is a sesquiterpene lactone with a 5-7-5 tricyclic skeleton, six chiral centers, and four exo-olefins. This natural product has numerous attractive biolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d9cbe6a4451ca7e51e7f485ffabec54
https://doi.org/10.1039/d1ob00657f
https://doi.org/10.1039/d1ob00657f
Autor:
Brian W. Skelton, Kersten Matthias Gericke, Jennette A. Sakoff, Scott G. Stewart, Yuki Egoshi, Jayne Gilbert, Kelly A. Young, James E. Rixson, James R. Abraham, Adam McCluskey
Publikováno v:
Bioorganicmedicinal chemistry. 23(13)
An efficient and divergent methodology for the synthesis of new anthracenone-pyranones and anthracenone-furans is described. Key reactions discussed in these syntheses include an aldehyde promoted annulation with a β-keto-sulfoxide, a domino alkyne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d053e3902ff96e000126bf3dae2c8b7
https://pubmed.ncbi.nlm.nih.gov/25979375
https://pubmed.ncbi.nlm.nih.gov/25979375
Publikováno v:
Tetrahedron Letters. 54:7029-7030
A three-step synthesis of (R)-7-hydroxycarvone (1), which is anticipated to be a valuable building block for the versatile preparation of natural products, is described. Optimization of the reaction conditions for photooxygenation and migration of (S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74ec52209f43665dee4761da7183efe9
https://doi.org/10.1016/j.tetlet.2013.10.066
https://doi.org/10.1016/j.tetlet.2013.10.066