32284-49-4Relevant academic research and scientific papers
Alkyne Cycloadditions Mediated by Tetrabutylammonium Fluoride: A Unified and Diversifiable Route to Isoxazolines and Pyrazolines
Nagy, Edith,Lepore, Salvatore D.
supporting information, p. 3695 - 3698 (2017/07/26)
A versatile approach to isoxazolines and pyrazolines by the cyclization of alkyne substrates using tetrabutylammonium fluoride (TBAF) is described. The reported diheteroatom cycles were produced under mild reaction conditions and with broad product scope.
Silyl isoxazolines-2: Synthesis, structure and properties
Lukevics,Dirnens,Kemme,Popelis
, p. 235 - 244 (2007/10/03)
Silyl isoxazolines have been synthesized by [2 + 3] cycloaddition reaction of nitrile oxides and silylnitronates to vinyl-and allylsilanes. The direction of the cycloaddition reaction of nitrile oxides to trialkoxyvinylsilanes has been shown to depend on
