Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tiaoling Dong"'
Publikováno v:
Heteroatom Chemistry. 15:193-198
Alkoxy-λ6-sulfanenitriles were found to be versatile alkylating reagents toward various nucleophiles bearing at least one proton such as methanol, phenol, thiophenols, carboxylic acids, p-toluenesulfonic acid, hydrochloric acid, and primary and seco
Autor:
Hiroyuki Morita, Huagang Dai, Takayoshi Fujii, Toshiaki Yoshimura, Tiaoling Dong, Shin Ono, Satoro Murotani, Choichiro Shimasaki
Publikováno v:
Bulletin of the Chemical Society of Japan. 74:945-954
A kinetic investigation on the hydrolysis of aryl(fluoro)(phenyl)-λ6-sulfanenitriles was carried out in some aqueous and mixed aqueous-organic solutions. The pH-rate profiles showed that the hydrolysis consists of pH-independent, acid-catalyzed and
Autor:
Hiroyuki Morita, Toshiaki Yoshimura, Youko Wakai, Mikiko Sakuta, Choichiro Shimasaki, Masanori Ohkubo, Takayoshi Fujii, Shin Ono, Tiaoling Dong
Publikováno v:
Bulletin of the Chemical Society of Japan. 73:957-965
The hydrolysis of alkoxy(aryl)(phenyl)-λ6-sulfanenitriles in several buffer solutions was found to follow a good pseudo-first-order kinetic equation, giving the corresponding sulfoximides and alcohols (for the case of the hydrolysis of neopentyloxy-
Publikováno v:
Energy & Fuels. 7:1123-1127
The physical density of a macromolecular model (C 390 H 362 O 38 ) for Japanese bituminous Akabira coal, which was previously constructed on the basis of the combined data of its Curie-point pyrolysis and CP/MAS 13 C NMR, and of four kinds of the sys
Publikováno v:
ChemInform. 35
Alkoxy-λ6-sulfanenitriles were found to be versatile alkylating reagents toward various nucleophiles bearing at least one proton such as methanol, phenol, thiophenols, carboxylic acids, p-toluenesulfonic acid, hydrochloric acid, and primary and seco