22606-85-5Relevant 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
Reduction of N-Substituted Azetidin-2-ones to Azetidines
Jackson, Mervyn B.,Mander, Lewis N.,Spotswood, Thomas M.
, p. 779 - 788 (2007/10/02)
Reduction of N-substituted azetidin-2-ones to N-substituted azetidines was accomplished rapidly and in good yield with diborane in tetrahydrofuran and with alane in ether.The stereochemistry of the ring substituents was retained under the reaction conditi
