259191-90-7Relevant academic research and scientific papers
A straightforward and versatile approach to the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles from alkyl halides via a one-pot, three-component reaction
González-Calderón, Davir,Aguirre-De Paz, José G.,González-González, Carlos A.,Fuentes-Benítes, Aydeé,González-Romero, Carlos
, p. 1713 - 1715 (2015)
The preparation of 1,4,5-trisubstituted 1,2,3-triazoles by the coupling of three components (alkyl halides, sodium azide, and active ketones) through an azide-enolate [3+2] cycloaddition (Dimroth cycloaddition) has been developed for the first time. A wide variety of halides (including chlorides, bromides, and iodides as well as primary and secondary derivatives) have demonstrated the versatility of this method, which is based on a one-pot system under mild reaction conditions.
A soluble iron(ii)-phthalocyanine-catalyzed intramolecular C(sp3)-H amination with alkyl azides
Che, Chi-Ming,Fan, Jianqiang,Kang, Fangyuan,Liu, Yungen,Wu, Liangliang,You, Tingjie,Zeng, Si-Hao
supporting information, p. 10711 - 10714 (2021/10/20)
Herein, we describe a soluble iron(ii)-phthalocyanine, [FeII(tBu4Pc)(py)2] (Pc = phthalocyaninato(2-)), as an effective catalyst in intramolecular C(sp3)-H bond amination, with alkyl azides as the nit
Dihydro-[1,2,3]triazolo-[4,5-d]pyrimidin-7-one
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, (2008/06/13)
The present invention relates to novel dihydro-[1,2,3]triazolo-[4,5-d]pyrimidin-7-one, to processes for their preparation and to their use as medicaments, in particular as inhibitors of cGMP-metabolizing phosphodiesterases.
