13427-53-7Relevant articles and documents
Conjugate Addition of Acylate-Nickel Complexes to Quinone Monoketals: Formal Synthesis of the Naphthoquinone Antibiotics Nanaomycin A and Deoxyfrenolicin
Semmelhack, M. F.,Keller, L.,Sato, T.,Spiess, E. J.,Wulff, W.
, p. 5566 - 5574 (1985)
A direct approach to the synthesis of isochromanone antibiotics such as nanaomycin A (2) and deoxyfrenolicin (3) is the conjugate addition of a carbonyl anion equivalent to the appropriate naphthoquinone monoketal followed by trapping with an allylic hali
PHENYL BENZYL ETHER DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOF
-
, (2017/06/12)
Parts of compounds, after being labeled by radionuclide, of the phenyl benzyl ether derivative, are used as Aβ plaque imaging agent. The structural formula of the phenyl benzyl ether derivative is shown by formula (I). The present invention develops a kin
Synthesis of N,N'-Bis(thioacetoxyalkoxy)piperazine and its self-assembled monolayer (SAM) formation on gold electrode
Xi, Haitao,Ju, Shenglan,Chen, Zhidong,Sun, Xiaoqiang
experimental part, p. 415 - 417 (2010/07/10)
A novel terminal thioacetate-substitued alkoxy piperazine was successfully synthesized from 4-(benzyloxy)phenol after six-step reaction and employed as the surface-active material in fabrication of self-assembled monolayers (SAMs). Cyclic voltammetric (CV) results showed that the SAM-modified gold electrode had special capacity in recognition for Fe3+.