Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yurio Kurita"'
Autor:
Kenji Azechi, Hiroaki Tokiwa, Yurio Kurita, Akira Takagi, Kozumo Saito, Takashi Ikawa, Yasuyuki Kita, Shuji Akai, Masahiro Egi, Yuji Itoh
Publikováno v:
Tetrahedron. 69:4338-4352
3-Borylbenzynes were generated in situ from 6-boryl-2-iodophenyl trifluoromethanesulfonates using i -PrMgCl·LiCl and applied to Diels–Alder reactions with substituted furans and pyrroles. The reactions allowed good functional group compatibility a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b360d449e4ff7faed7241212dabdf0e9
https://doi.org/10.1016/j.tet.2013.03.016
https://doi.org/10.1016/j.tet.2013.03.016
Autor:
Masahiro Egi, Yurio Kurita, Yasuyuki Kita, Kenji Azechi, Akira Takagi, Kozumo Saito, Keisuke Kakiguchi, Takashi Ikawa, Shuji Akai
Publikováno v:
Angewandte Chemie. 122:5695-5698
In situ generated unsymmetrically substituted borylbenzynes undergo the Diels—Alder reaction with furans or pyrroles to give highly functionalized arylboronic acid adducts with high or exclusive regioselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8638548fa6f294de22f5033baed5d09
https://doi.org/10.1002/ange.201002191
https://doi.org/10.1002/ange.201002191
Autor:
Kozumo Saito, Yasuyuki Kita, Keisuke Kakiguchi, Shuji Akai, Takashi Ikawa, Yurio Kurita, Masahiro Egi, Akira Takagi, Kenji Azechi
Publikováno v:
ChemInform. 41
In situ generated unsymmetrically substituted borylbenzynes undergo the Diels—Alder reaction with furans or pyrroles to give highly functionalized arylboronic acid adducts with high or exclusive regioselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f02ef7036fbeffa8f28cb2718f76d5e
https://doi.org/10.1002/chin.201050178
https://doi.org/10.1002/chin.201050178