Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tomomi Imai"'
Autor:
Ryosuke Matsui, Erina Niijima, Tomomi Imai, Hiroyuki Kobayashi, Akiko Hori, Azusa Sato, Yuko Nakamura, Osamu Kitagawa
Publikováno v:
Molecules, Vol 27, Iss 7, p 2369 (2022)
The halogen bond has been widely used as an important supramolecular tool in various research areas. However, there are relatively few studies on halogen bonding related to molecular chirality. 3-(2-Halophenyl)quinazoline-4-thione derivatives have st
Externí odkaz:
https://doaj.org/article/2664b8ec3fba4cff9f1e0d157ba3c7d0
Thionation of Optically Pure N-C Axially Chiral Quinazolin-4-one Derivatives with Lawesson’s Reagent
Publikováno v:
The Journal of Organic Chemistry. 86:709-715
The reaction of various optically pure N-C axially chiral quinazolin-4-one derivatives with Lawesson's reagent proceeded without a marked decrease in optical purity to give optically active quinazoline-4-thione derivatives (93-99% ee) possessing a hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6293d2f4725c3d86620081b131b34f97
https://doi.org/10.1021/acs.joc.0c02319
https://doi.org/10.1021/acs.joc.0c02319
Autor:
Akiko Hori, Vadim A. Soloshonok, Shumpei Terada, Osamu Kitagawa, Alicja Wzorek, Tomomi Imai, Erina Niijima
Publikováno v:
CrystEngComm. 21:3385-3389
In the crystals prepared from racemic axially chiral 3-(ortho-halophenyl)-2-methylquinazolin-4-one derivatives, the formation of intermolecular halogen bonding (CO⋯X) between the carbonyl oxygen and ortho-halogen atom (X = Cl, Br, I) was found, whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9132899d841c9141d5419b5e75ea08fe
https://doi.org/10.1039/c9ce00320g
https://doi.org/10.1039/c9ce00320g
Autor:
Tomomi Imai, Takuma Hosaka, Alicja Wzorek, Anna Kolbus, Karel D. Klika, Magdalena Marcinkowska, Vadim A. Soloshonok, Osamu Kitagawa
Publikováno v:
Amino Acids. 51:283-294
α-Amino acids (α-AAs) are in extremely high demand in nearly every sector of the food and health-related chemical industries and continue to be the subject of intense multidisciplinary research. The self-disproportionation of enantiomers (SDE) is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8ad0b989cd236e4a5ce6d0b33ad7e4e
https://doi.org/10.1007/s00726-018-2664-x
https://doi.org/10.1007/s00726-018-2664-x