Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yoshiyasu Kaimori"'
Publikováno v:
Chemical communications (Cambridge, England). 57(85)
Mechanistic understanding of the asymmetric autocatalysis of pyrimidyl alkanol is a highly attractive and challenging topic due to its unique feature of amplification of enantiomeric excess. Circular dichroism spectroscopic analysis of this reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d732ba83ff9db87eb2ce53f3607a95d
https://pubmed.ncbi.nlm.nih.gov/34622895
https://pubmed.ncbi.nlm.nih.gov/34622895
Autor:
Susumu Sato, Yoshiyasu Kaimori, Kenta Suzuki, Seiya Shimada, Tsuneomi Kawasaki, Arimasa Matsumoto, Natsuki Hara, Toru Asahi, Kenso Soai
Publikováno v:
Chemical communications (Cambridge, England). 57(49)
Triglycine sulfate (TGS) acts as a chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess, i.e., the Soai reaction. Therefore, molecular chirality of highly enantioenriched organic compounds is controlled by a ferroelec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a4fc6e0cbb03a564d02bb73c1e461f
https://pubmed.ncbi.nlm.nih.gov/34023863
https://pubmed.ncbi.nlm.nih.gov/34023863
Autor:
Kohei Higashiguchi, Kentaro Takano, Genki Sugiyama, Masashi Okaniwa, Hiroki Yamazaki, Yoshiyasu Kaimori, Tsuyoshi Kida, Kojiro Abe
Publikováno v:
2020 IEEE 8th Electronics System-Integration Technology Conference (ESTC).
TCB (Thermal Compression Bonding) with NCF (Non Conductive Film) is expected as an effective solution to realize fine pitch interconnections, however, the actual production volume is still small due to its low productivity. Although some multiple die
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b1278c38d91af1d4b78a81271e1fd21
https://doi.org/10.1109/estc48849.2020.9229782
https://doi.org/10.1109/estc48849.2020.9229782
Publikováno v:
Chemical communications (Cambridge, England). 55(36)
Among several theories proposed for the origin of homochirality, absolute asymmetric synthesis is unique because it produces chiral compounds without the intervention of any chiral factor. Here we report on the kinetically controlled heterogeneous so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7439cb45d351de59fc503e5a1fb6d2
https://pubmed.ncbi.nlm.nih.gov/30968100
https://pubmed.ncbi.nlm.nih.gov/30968100
Autor:
Mohamed Amedjkouh, Béla Barabás, Franco Bellesia, Thomas Buhse, Luciano Caglioti, Christophe Coudret, Joaquim Crusats, José-Manuel Cruz, János Csapó, Zoubir El-Hachemi, Csaba Fehér, Bálint Fridrich, Norihiko Fujii, Noriko Fujii, Ottilia Fülöp, Matías Funes-Maldonado, David Hochberg, Yoshiyasu Kaimori, Tsuneomi Kawasaki, Róbert Kurdi, Gábor Lente, Arimasa Matsumoto, Paul G. Mezey, Jean-Claude Micheau, László T. Mika, Albert Moyano, María E. Noble-Terán, Gyula Pályi, Máté Papp, Francesca Parenti, Adriano Pinetti, Josep M. Ribó, Valeria Righi, Carlo Romagnoli, Hiroaki Sakaue, Itaru Sato, Luisa Schenetti, Bora Sieng, Livia Simon-Sarkadi, Rita Skoda-Földes, Kenso Soai, Takumi Takata, Francesco Tassinari, József M. Tukacs, Béla Urbán, Guillem Valero, Bart Weimer, Claudia Zucchi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da021258e422b6a2b3e3d693e43f878
https://doi.org/10.1016/b978-0-12-812824-4.00028-9
https://doi.org/10.1016/b978-0-12-812824-4.00028-9
Chiral crystallization of achiral compounds is attracting much attention, especially in areas of chirality research such as chiral separation and generation. Spontaneous chiral crystallization generates chirality and is a possible origin of homochira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dbc6c3848425578447c30585b5add3f
https://doi.org/10.1016/b978-0-12-812824-4.00018-6
https://doi.org/10.1016/b978-0-12-812824-4.00018-6
Publikováno v:
Chemistry Letters. 44:688-690
Achiral ethylenediamine forms chiral structures spontaneously when crystallized as the sulfate salt. By using these chiral crystals of ethylenediamine sulfate (ethylenediammonium sulfate), asymmetr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95ad37bfed4cfb19bb8218cedf9111a9
https://doi.org/10.1246/cl.150052
https://doi.org/10.1246/cl.150052
Autor:
Yoshiyasu Kaimori, Tsuneomi Kawasaki, Mizuki Uchida, Kenso Soai, Arimasa Matsumoto, Haruna Omori
Publikováno v:
Angewandte Chemie (International ed. in English). 56(2)
Achiral inorganic gypsum (CaSO4 ⋅2 H2 O) triggers the asymmetric autocatalysis of pyrimidyl alkanol on its two-dimensional enantiotopic faces to give highly enantioenriched alkanol products with absolute configurations corresponding to the respecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d5312c1575ccc38749465588418260a
https://pubmed.ncbi.nlm.nih.gov/27906493
https://pubmed.ncbi.nlm.nih.gov/27906493
Publikováno v:
ChemInform. 46
Achiral ethylenediamine forms chiral structures spontaneously when crystallized as the sulfate salt.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fd3969d19410d6f17289a370ec98de3
https://doi.org/10.1002/chin.201534032
https://doi.org/10.1002/chin.201534032
Publikováno v:
Tetrahedron: Asymmetry. 24:1365-1367
An achiral nucleobase cytosine forms an achiral monohydrate crystal (space group: P21/c) by crystallization from a water solution. It was found that the removal of crystal water under reduced pressure at room temperature afforded a chiral crystal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d69ec596df0822822b39b4722f0bc012
https://doi.org/10.1016/j.tetasy.2013.09.020
https://doi.org/10.1016/j.tetasy.2013.09.020