Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Takayuki Wakaki"'
Autor:
Xiao Feng Wei, Hong Liang Li, Motomu Kanai, Aya Miyazaki, Taisuke Itoh, Kounosuke Oisaki, Yohei Shimizu, Miho Hatanaka, Takayuki Wakaki, Takayoshi Yoshimura
Publikováno v:
Chem. 5:585-599
Summary Chiral allenes are highly valuable as versatile synthetic intermediates and core skeletons of various functional organic molecules. Despite marked recent advances, the straightforward catalytic enantioselective synthesis of hydrocarbon allene
Autor:
Kentaro Sakai, Takayuki Wakaki, Mio Kondo, Shigeyuki Masaoka, Kounosuke Oisaki, Takafumi Enomoto, Motomu Kanai
Publikováno v:
Chemistry - A European Journal. 24:8051-8055
Inspired by the reaction mechanism of photo-induced DNA cleavage in nature, a C(sp3 )-H cyanation reaction promoted by visible-light photoredox/phosphate hybrid catalysis was developed. Phosphate radicals, generated by one-electron photooxidation of
Publikováno v:
ACS Catalysis. 8:3123-3128
We developed a palladium-catalyzed C–H transformation that enabled the synthesis of ketones from aldehydes and (hetero)aryl halides. The use of picolinamide ligands was key to achieving the transformation. Heteroaryl ketones, as well as diaryl keto
Autor:
Takayuki, Wakaki, Kentaro, Sakai, Takafumi, Enomoto, Mio, Kondo, Shigeyuki, Masaoka, Kounosuke, Oisaki, Motomu, Kanai
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(32)
Inspired by the reaction mechanism of photo-induced DNA cleavage in nature, a C(sp
Publikováno v:
Green Chemistry. 18:3681-3683
The generation and utilisation of toxic side-products is discussed in this Editorial, part of a series celebrating the Twelve Principles of Green Chemistry.
Autor:
Mio Kondo, Takayuki Wakaki, Motomu Kanai, Shigeyuki Masaoka, Takafumi Enomoto, Kentaro Sakai, Kounosuke Oisaki
Publikováno v:
Chemistry - A European Journal. 24:8018-8018
Publikováno v:
ChemInform. 46
An efficient method for C7-position-selective alkenylation of N-substituted indolines with alkenes is reported. Various 7-alkenylindolines were obtained in moderate to excellent yields in air in the presence of catalytic amounts of [Cp*IrCl2]2, AgOTf
Publikováno v:
ChemInform. 46
The reaction exhibits a wide substrate scope, and a variety of π-conjugated molecules is synthesized in high yields, even in gram scale.
Publikováno v:
Organic letters. 17(7)
We successfully developed an iridium-catalyzed ortho-selective C–H silylation of aromatic compounds. The reaction exhibited a wide substrate scope, and a variety of π-conjugated molecules were synthesized in good to excellent yields, even in gram
Publikováno v:
Chemistry, an Asian journal. 9(5)
An efficient method for C7-position-selective alkenylation of N-substituted indolines with alkenes is reported. Various 7-alkenylindolines were obtained in moderate to excellent yields in air in the presence of catalytic amounts of [Cp*IrCl2]2, AgOTf