Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Arihiro Saito"'
Autor:
Saika Otsubo, Hiroshi Imahori, Yoshihiro Matano, Seiji Akiyama, Tooru Miyajima, Shinji Aramaki, Emi Nakamoto, Arihiro Saito, Yuto Suzuki
Publikováno v:
Chemistry - An Asian Journal. 7:2305-2312
A divergent method for the synthesis of α,α'-diarylacenaphtho[1,2-c]phosphole P-oxides has been established; α,α'-dibromoacenaphtho[c]phosphole P-oxide, which was prepared through a Ti(II)-mediated cyclization of 1,8-bis(trimethylsilylethynyl)nap
Autor:
Yoshihiro Matano, Furitsu Suzuki, Arihiro Saito, Daisuke Sakamaki, Kazuyoshi Tanaka, Yasuaki Tokudome, Hironori Kaji, Hiroshi Imahori, Akihiro Ito, Tatsuya Fukushima
Publikováno v:
Angewandte Chemie. 123:8166-8170
A profusion of phospholes: Diacenaphtho[1,2-b:1',2'-d]phospholes, a new class of arene-fused phosphole π-systems, were synthesized and their structural and electrochemical properties studied. The P-sulfide derivative has a high electron-transporting
Publikováno v:
Heteroatom Chemistry. 22:457-470
2,5-Bis(1,5-diphenylphosphol-2-yl)he-terole derivatives were prepared via Pd-catalyzed Stille-type cross-coupling reactions of α-(tributylstannyl) phosphole or α-iodophosphole with the corresponding 2,5-difunctionalized heteroles (pyrrole, furan, a
Publikováno v:
COMPTES RENDUS CHIMIE. 13(8-9):1035-1047
2,5-Bis(pyrrol-2-yl)phosphole derivatives were prepared using the reaction of titanacycles, generated in situ from a TiII reagent and pyrrole-capped 1,6-heptadiynes, with dichloro(phenyl)phosphine. The 2,5-bis(pyrrol-2-yl)phosphole derivatives were f
Autor:
Tooru Miyajima, Makoto Nakashima, Tatsuya Fukushima, Hironori Kaji, Arihiro Saito, Hiroshi Imahori, Yoshihiro Matano
Publikováno v:
Chemistry - A European Journal. 15:10000-10004
Autor:
Yusuke Kon, Hiroshi Imahori, Toshihiro Murafuji, Yoshifumi Kimura, Arihiro Saito, Yoshihiro Matano
Publikováno v:
Chemistry Letters. 40:919-921
Divergent synthesis of 2,5-diarylphosphole derivatives was achieved by using two kinds of Pd-catalyzed cross-coupling reactions. In addition, para- and P-substituent effects on the optical and redo...
Publikováno v:
Organic letters. 15(4)
A new class of polyphospholes bearing alkanesulfonylimino moieties on the phosphorus(V) centers was prepared by the Pd-CuI-promoted Stille coupling reaction to investigate the charge-carrier transport properties of the π-networks of polyphospholes.
Autor:
Yusuke Kon, Toshihiro Murafuji, Yoshifumi Kimura, Hiroshi Imahori, Yoshihiro Matano, Arihiro Saito
Publikováno v:
ChemInform. 43
Two kinds of Pd-catalyzed cross-coupling reactions are employed to synthesize diarylphospholes (III) and (VII) (Stille coupling), and (X) (Negishi coupling).
Publikováno v:
ChemInform. 42
A convenient method for the synthesis of the title compounds (III), (IV), (VII), and (IX) is established.
Publikováno v:
Organic letters. 12(11)
Palladium-copper-promoted Stille-type cross-coupling reactions between alpha-stannylphospholes and alpha-iodophospholes afforded alpha,alpha'-linked oligophospholes and polyphosphole efficiently. It has been revealed that the polyphosphole P-oxide po