25674-67-3Relevant academic research and scientific papers
Reaction of 1-nitroso-2-naphthols with α-functionalized ketones and related compounds: The unexpected formation of decarbonylated 2-substituted naphtho[1,2-d][1,3]oxazoles
Aljaar, Nayyef,Malakar, Chandi C.,Conrad, Ju Rgen,Frey, Wolfgang,Beifuss, Uwe
, p. 154 - 166 (2013/03/28)
Reactions between 1-nitroso-2-naphthols and α-functionalized ketones such as α-bromo-, α-chloro-, α-mesyloxy-, α-tosyloxy-, and α-hydroxy ketones under basic conditions delivered 2-substituted naphtho[1,2-d][1,3]oxazoles in a single synthetic operation. T
Microwave-induced 1,3-dipolar cycloaddition of 2-aroyl-aziridines
Boruah, Anima,Baruah, Bipul,Prajapati, Dipak,Sandhu, Jagir S.,Ghosh, Anil C.
, p. 4203 - 4204 (2007/10/03)
2-Aroyl-aziridines react with a variety of multiple bonds under microwave irradiation in an Erlenmeyer flask at ambient pressure to give the corresponding cycloadducts in high yields within few minutes.
