Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Masataka Takashika"'
Autor:
Masataka Takashika, Kazunori Hirabayashi, Masahiko Iyoda, Keitaro Yamamoto, Masashi Hasegawa, Yutaka Ie, Shinobu Aoyagi, Keigo Shirahata, Hiroyuki Otani, Toshio Shimizu
Publikováno v:
The Journal of Organic Chemistry. 86:302-309
McMurry coupling is one of the most useful and convenient tools for the preparation of π-conjugated molecules. However, for the synthesis of strained macrocycles containing ethynylene linkages, reduction of ethynylene to vinylene linkage sometimes t
Autor:
Shinobu Aoyagi, Kazuhira Miwa, Hiroyuki Otani, Saori Mizuno, Wakana Kariya, Toshihiro Fujiwara, Masahiko Iyoda, Hideyuki Shimizu, Masashi Hasegawa, Masataka Takashika
Publikováno v:
Journal of the American Chemical Society. 142:13662-13666
A phenyl-substituted macrocyclic π-extended thiophene hexamer 1, composed of four thienylene-ethynylene and two thienylene-vinylene units, has a solid-state structure in which π–π, CH−π, and van de...
Autor:
Toshihiro Fujiwara, Masataka Takashika, Masashi Hasegawa, Yoshio Aso, Yutaka Ie, Shinobu Aoyagi, Masahiko Iyoda, Hiroyuki Otani
Publikováno v:
ChemPlusChem. 84(6)
Three new macrocyclic π-extended thiophene hexamers composed of four thienylene-ethynylene and two thienylene-vinylene units with or without four alkyl substituents have been synthesized. Despite similar shape-persistent structures in solution, the
Autor:
Atsumi Shirai, Yuki Nakamura, Shin-ichiro Kato, Hiroyuki Otani, Masataka Takashika, Masahiko Iyoda, Hiroto Sano, Masashi Hasegawa
Publikováno v:
The Journal of organic chemistry. 83(7)
Macrocyclic 10-mesityl-1,8-diphenylanthracene dimer 4 was synthesized by using the electron-transfer oxidation of Lipshutz cuprate derived from 1,8-bis(4-bromophenyl)-10-mesityl-anthracene 7 in moderate yield. This dimer 4 is a considerably fluoresce
Autor:
Masahiko Iyoda, Masataka Takashika, Masashi Hasegawa, Hiroyuki Otani, Saori Mizuno, Kazuhira Miwa, Wakana Kariya, Toshihiro Fujiwara, Hideyuki Shimizu, Shinobu Aoyagi
Publikováno v:
Journal of the American Chemical Society; 8/12/2020, Vol. 142 Issue 32, p13662-13666, 5p
Publikováno v:
HETEROCYCLES. 97:1313