1269460-63-0Relevant academic research and scientific papers
Synthesis of 2-phenyl- and 2,2-diarylpyrrolidines through Stevens rearrangement performed on azetidinium ions
Drouillat, Bruno,D'Aboville, Edouard,Bourdreux, Flavien,Couty, Francois
supporting information, p. 1103 - 1109 (2014/03/21)
A set of azetidinium ions substituted at the nitrogen atom either by a benzyl group or a benzhydryl group were synthesized to delineate the scope of their ring expansion into 2-phenyl- or 2,2-diaryl-pyrrolidines through a Stevens rearrangement. Whereas th
Synthesis of 2-Phenyl- and 2,2-Diarylpyrrolidines through Stevens Rearrangement Performed on Azetidinium Ions
Drouillat, Bruno,D'Aboville, Edouard,Bourdreux, Flavien,Couty, Fran?ois
supporting information, p. 1103 - 1109 (2015/10/05)
A set of azetidinium ions substituted at the nitrogen atom either by a benzyl group or a benzhydryl group were synthesized to delineate the scope of their ring expansion into 2-phenyl- or 2,2-diaryl-pyrrolidines through a Stevens rearrangement. Whereas th
Ring expansion of 2-(1-Hydroxyalkyl)azetidines to 4-(2-Chloroethyl) oxazolidinones
Couty, Francois,Drouillat, Bruno,Lemee, Frederic
, p. 794 - 801 (2011/03/22)
2-(1-Hydroxyalkyl)azetidines react with bis(trichloromethyl) carbonate (BTC) after basic treatment to afford 4-(2-chloroethyl)oxazolidinones. The scope of this rearrangement was examined in detail and its efficiency was shown to depend on the class of the
