Pyrrolidines from β-Aminoselenides via Radical Cyclization. Diastereoselectivity Control by the N-Substituent
(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
Besev, Magnus,Engman, Lars
p. 1589 - 1592
(2007/10/03)
More Articles about upstream products of 281669-99-6