作者:Masanori Kawasaki、Hisashi Yamamoto
DOI:10.1021/ja066726y
日期:2006.12.1
This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained hetero-Diels-Alder adduct was easily converted to the corresponding chiral 1,4-diamino alcohol.
本通讯描述了使用偶氮吡啶作为试剂和银作为催化剂以高区域和对映选择性提供偶氮杂-狄尔斯-阿尔德加合物的研究。获得的杂狄尔斯-阿尔德加合物很容易转化为相应的手性 1,4-二氨基醇。