Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ohji Watanabe"'
Autor:
Takayoshi Arai, Kodai Horigane, Ohji Watanabe, Junki Kakino, Noriyuki Sugiyama, Hiroki Makino, Yuto Kamei, Shinnosuke Yabe, Masahiro Yamanaka
Publikováno v:
iScience, Vol 12, Iss , Pp 280-292 (2019)
Summary: Cooperative activation using halogen bonding and hydrogen bonding works in metal-catalyzed asymmetric halolactonization. The Zn3(OAc)4-3,3′-bis(aminoimino)binaphthoxide (tri-Zn) complex catalyzes both asymmetric iodolactonization and bromo
Externí odkaz:
https://doaj.org/article/9502e03c9184489d9f24308a2c614ff2
Autor:
Hiroki Makino, Shinnosuke Yabe, Takayoshi Arai, Masahiro Yamanaka, Noriyuki Sugiyama, Yuto Kamei, Ohji Watanabe, Junki Kakino, Kodai Horigane
Publikováno v:
iScience, Vol 12, Iss, Pp 280-292 (2019)
iScience
iScience
Summary Cooperative activation using halogen bonding and hydrogen bonding works in metal-catalyzed asymmetric halolactonization. The Zn3(OAc)4-3,3′-bis(aminoimino)binaphthoxide (tri-Zn) complex catalyzes both asymmetric iodolactonization and bromol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85844c90f335f9812fe8c79b06ca67d
https://doi.org/10.1016/j.isci.2019.01.029
https://doi.org/10.1016/j.isci.2019.01.029
Publikováno v:
ChemCatChem. 7:3234-3238
On the basis of the structure of the unimolecular Zn3(OAc)4–3,3′-bis(aminoimino)binaphthoxide complex, a poly-Zn3(OAc)4–3,3′-bis(aminoimino)binaphthoxide (poly-Zn) complex was prepared from 3,3′-diformylbinaphthol, tetramine, and Zn(OAc)2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e58a1a003f52b4379fd9414b65a5cb18
https://doi.org/10.1002/cctc.201500842
https://doi.org/10.1002/cctc.201500842
Publikováno v:
ChemInform. 47
On the basis of the structure of the unimolecular Zn3(OAc)4–3,3′-bis(aminoimino)binaphthoxide complex, a poly-Zn3(OAc)4–3,3′-bis(aminoimino)binaphthoxide (poly-Zn) complex was prepared from 3,3′-diformylbinaphthol, tetramine, and Zn(OAc)2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7d9cb44e0ccf8e821fd5e4816474bb5
https://doi.org/10.1002/chin.201608159
https://doi.org/10.1002/chin.201608159
Publikováno v:
ChemInform. 47
A newly developed aminoiminophenoxy copper carboxylate (L7-Cu-OAc)-catalyzed asymmetric iodocyclization of N-Tosyl alkenamides gave O-cyclized products in good yields with high enantioselectivity. From the O-cyclized products, a skeletal transformati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8978e2d0d1b410d1b329a85241b84285
https://doi.org/10.1002/chin.201610023
https://doi.org/10.1002/chin.201610023
Publikováno v:
ChemCatChem. 7:3405-3405
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f1dea70fbc32332f04f665528c6dbad
https://doi.org/10.1002/cctc.201501071
https://doi.org/10.1002/cctc.201501071