Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Youichi Inada"'
Autor:
Sakae Uemura, Yoshihiro Miyake, Ken Sakata, Keiichiro Kanao, Masato Yoshikawa, Masaki Daini, Youichi Inada, Yoshiaki Nishibayashi
Publikováno v:
Organometallics. 27:2046-2051
Ruthenium-catalyzed carbon−carbon bond forming reactions between propargylic alcohols and acyclic and cyclic 1,3-conjugated dienes give the corresponding dienyne compounds in good to high yields. Only the use of thiolate-bridged diruthenium complex
Autor:
Sakae Uemura, Masanobu Hidai, Gen Onodera, Youichi Inada, Hiroaki Imajima, Yoshiaki Nishibayashi
Publikováno v:
Organometallics. 23:5100-5103
Various alkanechalcogenolate (SR, SeR, TeR)- and benzenechalcogenolate (SPh, SePh, TePh)-bridged diruthenium complexes have been newly prepared, and their catalytic activity toward the propargylation of acetone with propargylic alcohol has been inves
Autor:
Sakae Uemura, Yoshiaki Nishibayashi, Youichi Inada, Masato Yoshikawa, Masanobu Hidai, Marilyn Daisy Milton
Publikováno v:
Angewandte Chemie International Edition. 42:2681-2684
Publikováno v:
Angewandte Chemie International Edition. 42:1495-1498
Publikováno v:
Organometallics. 22:873-876
Novel diruthenium complexes containing chiral thiolate-bridged ligands are synthesized and characterized crystallographically. The chiral diruthenium complexes promote enantioselective propargylic alkylation of propargylic alcohols with acetone to gi
Autor:
Keiko Imamura, Mamoru Fukuda, Yoshihiro Kato, Norishige Ehara, Haruki Ogata, Youichi Inada, Yasuo Nakajima
Publikováno v:
Nihon Nyugan Kenshin Gakkaishi (Journal of Japan Association of Breast Cancer Screening). 10:259-265
Publikováno v:
ChemInform. 33
Novel ruthenium-catalyzed cycloaddition of propargylic alcohols with 2-naphthols and phenols bearing electron-donating groups via allenylidene intermediates has been developed to give the corresponding 1H-naphtho[2,1-b]pyrans and 4H-1-benzopyrans, re
Autor:
Keiichiro Kanao, Sakae Uemura, Youichi Inada, Yoshihiro Miyake, Masato Yoshikawa, Yoshiaki Nishibayashi, Ken Sakata, Masaki Daini
Publikováno v:
ChemInform. 39
Ruthenium-catalyzed carbon−carbon bond forming reactions between propargylic alcohols and acyclic and cyclic 1,3-conjugated dienes give the corresponding dienyne compounds in good to high yields. Only the use of thiolate-bridged diruthenium complex
Autor:
Yoshihiro Miyake, Yoshiaki Nishibayashi, Sakae Uemura, Masahiro Yuki, Youichi Inada, Yoshihiro Yamauchi, Yoshiaki Tanabe
Publikováno v:
ChemInform. 39
Novel ruthenium-catalyzed vinylic substitution reactions of vinylic trifluoromethanesulfonates with nucleophiles such as cyclic 1,3-diketones and alcohols have been found to give the corresponding vinylic-substituted products in good to high yields.
Publikováno v:
ChemInform. 37