作者:Yeon-Hee Lim、Tindy Li、Peiling Chen、Patrick Schreiber、Larissa Kuznetsova、Patrick J. Carroll、Joseph W. Lauher、Scott McN. Sieburth
DOI:10.1021/ol052071e
日期:2005.11.1
Halogenation of achiral trans-2-pyridone photodimers results in 1,3-migration of an amide nitrogen and formation of a chiral structure with six stereogenic centers and well-differentiated functionality. The reactivity of this product toward nucleophiles, including the allylic halide, is dominated by participation by the amide nitrogen.