Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

2,2’-dithiobis nitropyridine

ND = Not determined DTNB 2,2 -Dithiobis(5-nitropyridine) DTNP 2,2 -Dithiobis(5-nitrobenzoate) DEDC Diethyldithiocarbamate IA Iodoacetate NEM N-ethylmaleimide PCMB p-chloromercuribenzoate 1, 10-PT 1, 10-phenanthroline 8-Q 8-Quinolinol 2, 2 -BP 2, 2 -Bipyridyl. [Pg.94]

Kumar et al. [268] have described a similar support based on 3-mercaptopropyl CPG (SSgrnolg 1). It has been treated with 2,2 -dithiobis(5-nitropyridine) followed by the O-dimethoxytritylated mercaptoethanol to furnish the unsymmetrical disul-... [Pg.556]

Sulphite and thiosulphate have been determined by liquid chromatography after derivati-zation with 2,2 -dithiobis(5)nitropyridine (Vairavanmurthy and Mapper, 1990). At high levels of H2S sulphide should be precipitated with ZnCl2 Millero, 1991). [Pg.107]

Copper(I)-catalyzed amination of iodobenzene with aniline in the presence of KO-t-Bu as base was described by Don and co-workers [56] (Scheme 22.12). They reported the use of the [Cu2(p-I)2(L)2] (L = l,2-bis(diphenylphosphino)-c/oi 0-carborane(12) (1)) catalyst, which showed a conversion of the amine of 58%, compared to no significant conversion without ligand 1. The conversion is in the range of the reaction of copper(I) iodide in the presence of 2,2 -dithiobis(5-nitropyridine) but lower than that of the 2,2 -bipyridine ligand [57]. It was postulated that the reaction proceeds via an insertion of the copper(I) species into the carbon-halogen bond as the initial step. [Pg.557]


See other pages where 2,2’-dithiobis nitropyridine is mentioned: [Pg.246]    [Pg.248]    [Pg.489]    [Pg.561]    [Pg.561]    [Pg.398]    [Pg.220]    [Pg.5419]    [Pg.106]    [Pg.106]    [Pg.119]    [Pg.463]    [Pg.463]    [Pg.1015]    [Pg.1090]    [Pg.1174]    [Pg.1296]   
See also in sourсe #XX -- [ Pg.10 , Pg.230 , Pg.367 , Pg.384 ]




SEARCH



2- 5-nitropyridine

5,5 -Dithiobis

© 2024 chempedia.info