100712-22-9Relevant academic research and scientific papers
Reductive Hydrazination with Trichlorosilane: A Method for the Preparation of 1,1-Disubstituted Hydrazines
Wang, Tao,Di, Xiao,Wang, Chao,Zhou, Li,Sun, Jian
supporting information, p. 1900 - 1903 (2016/05/19)
A straightforward and facile method has been developed to prepare 1,1-disubstituted hydrazines via Lewis base promoted direct reductive hydrazination. Under the catalysis of hexamethylphosphoramide (HMPA) and N,N-dimethylacetamide (DMAc), respectively, various ketones and aldehydes could react with phenylhdrazines to prepare 1,1-disubstituted hydrazines with good to high yields.
2,3′-Bis(1′H-indole) heterocycles: New p53/MDM2/MDMX antagonists
Neochoritis, Constantinos G.,Wang, Kan,Estrada-Ortiz, Natalia,Herdtweck, Eberhardt,Kubica, Katarzyna,Twarda, Aleksandra,Zak, Krzysztof M.,Holak, Tad A.,D?mling, Alexander
supporting information, p. 5661 - 5666 (2015/11/24)
The protein-protein interaction of p53 and MDM2/X is a promising non genotoxic anticancer target. A rapid and efficient methodology was developed to synthesize the 2,3′-bis(1′H-indole) heterocyclic scaffold 2 as ester, acid and amide derivatives. Their binding affinity with MDM2 was evaluated using both fluorescence polarization (FP) assay and HSQC experiments, indicating good inhibition and a perfect starting point for further optimizations.
A convenient synthesis of 1-alkyl-1-phenylhydrazines from N-aminophthalimide
Nara, Shigeru,Sakamoto, Takeshi,Miyazawa, Etsuko,Kikugawa, Yasuo
, p. 87 - 98 (2007/10/03)
N-Alkylaminophthalimides were synthesized by condensation of N-aminophthalimide with aldehydes, and subsequent reduction of the intermediate with pyridine-borane in acetic acid. N-Phenylation and removal of the phthalimide group gave 1-alkyl-1-phenylhydrazines in high yield.
