281669-83-8Relevant academic research and scientific papers
Rhodium-catalyzed stereoselective formation of Z-enamines from allylaziridines
Alphonse, France-Aimee,Yudin, Andrei K.
, p. 11754 - 11755 (2006)
Rhodium (I)-catalyzed isomerization of N-allylaziridines affords isolable Z-enamines in excellent yields and with high stereoselectivity. Cationic [Rh(BINAP)(COD)]OTf and RhH(CO)(PPh3)3 follow the same selectivity toward the Z-isomer
Pyrrolidines from β-Aminoselenides via Radical Cyclization. Diastereoselectivity Control by the N-Substituent
Besev, Magnus,Engman, Lars
, p. 1589 - 1592 (2007/10/03)
(Matrix Presented) N-Allyl-β-aminoalkyl phenyl selenides - precursors of 3-aza-5-hexenyl radicals - were prepared by ring opening of N-allylaziridines with benzeneselenol under acidic conditions or by sodium cyanoborohydride reduction of N-allylimines of
