864515-66-2Relevant academic research and scientific papers
Synthesis, Characterization, and Reactivity of Metalla-Chalcogenirenium Compounds?
Cai, Yapeng,Lin, Xinlei,Long, Lipeng,Luo, Ming,Xia, Haiping,Zhang, Hong
, p. 1558 - 1564 (2021)
Chalcogenirenium cations, featuring an unsaturated three-membered organic ring, are limited but known to be synthesizable from alkynes with bulky electron-donating groups. Metalla-chalcogenirenium compounds have been synthesized as stable compounds throug
Azulen-1-yl diazenes substituted at C-3 with phenyl-chalcogene moieties: Dye synthesis, product characterization and properties
Razus, Alexandru C.,Birzan, Liviu,Cristea, Mihaela,Dragu, Eugenia Andreea,Hanganu, Anamaria
experimental part, p. 1271 - 1282 (2012/06/04)
Two synthesis strategies were used for the generation of azulene-1-yl diazenes substituted at C-3 with a phenyl-chalcogenyl moiety, the synthesis of azulenes substituted at C-3 followed by azo-coupling and azulene substitution at C-3 in azulene-azo dyes.
Facile synthesis of β-organotellurobutenolides via electrophilic tellurolactonization of α-allenoic acids
Xu, Qing,Huang, Xian,Yuan, Jingqi
, p. 6948 - 6951 (2007/10/03)
We report a convenient and highly efficient method for the synthesis of β-organotellurobutenolides by the aryltellurenyl halides-induced electrophilic tellurolactonization of α-allenoic acids under mild conditions. The resulting β-organotellurobutenolides
