53942-65-7Relevant academic research and scientific papers
Flash vacuum pyrolysis of 2-diazo-8-oxabicyclo[3.2.1]oct-6-en-3-ones. A new method for the preparation of propadienones
Brahms,Dailey
, p. 1381 - 1384 (2007/10/02)
When diazoketones 3a and 3b are pyrolysed at 430°C and 10-4 torr, they undergo loss of N2 followed by Wolff rearrangement and loss of furan by retro Diels-Alder reaction to yield the desired propadienones 1(a,b). If argon is added to the pyrolysate mixture, these reactive compounds can be trapped under matrix isolation conditions at 22 K and observed by FTIR. Upon photolysis, 1b yields carbon monoxide and 2-butyne.
LOW TEMPERATURE KETENE PREPARATIONS USING NITROSYLTETRACARBONYLCHROMIUM (-II) ANION
Masters, A. P.,Sorensen, T. S.
, p. 5869 - 5872 (2007/10/02)
Methylene and cyclopropyl ketenes can be generated at -100 deg C by the dehalogenation of α-bromoacylhalides using nitrosyltetracarbonylchromium (-II) anion.This facilitates the trapping of these ketenes with more stable ketenes to give mixed ketene dimers.
