73620-31-2Relevant articles and documents
Generation and rearrangements of ylides from tertiary amines and α-diazo ketones - Very high catalytic activity of [RuCl(η5-C5H5)(PPh3) 2]
Del Zotto, Alessandro,Baratta, Walter,Miani, Francesca,Verardo, Giancarlo,Rigo, Pierluigi
, p. 3731 - 3735 (2007/10/03)
The reaction of N,N-dimethyl-2-propen-1-amine, N,N-dimethylbenzylamine and N,N-dimethyl-2-propyn-1-amine with the α-diazo ketones N2CHCOR [R = Me (2a), Et (2b), nPr (2c), iPr (2d), (CH2)10Me (2e), (CH2)14/
INVESTIGATIONS IN THE AREA OF AMINES AND AMMONIUM COMPOUNDS. CLIII. STEVENS REARRANGEMENT UNDER THE INFLUENCE OF SODIUM
Kocharyan, S. T.,Razina, T. L.,Ogandzhanyan, S. M.,Babayan, A. T.
, p. 1256 - 1260 (2007/10/02)
The Stevens rearrangement was realized in ammonium salts containing a phenacyl, alkoxycarbonylmethyl, acetonyl, or cyanomethyl group in addition to a β,γ-unsaturated group by the action of metallic sodium.