摘要
首次实现了铑催化的烯基氮杂环丙烷与炔胺底物的立体专一性的分子间[3+2]环加成反应.该反应具有较好的底物兼容性,反应条件温和,操作简便.此外,烯基氮杂环丙烷原料的手性可完全转移至环加成产物中,这为原子经济性且对映选择性地合成重要的2-氨基吡咯啉类衍生物提供了新的策略.
The first rhodium-catalyzed stereospecific intermolecular [3＋2] cycloaddition reaction of vinylaziridines with ynamides was realized. The salient features of the transformation include broad substrate scope, mild reaction condition, and simple operation. Moreover, the chiratity of vinylaziridines can be completely transferred to the cycloadducts, representing an atom-economic and enantiospecific protocol for the construction of valuable 2-amino pyrroline derivatives.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2017年第5期1165-1172,共8页
Chinese Journal of Organic Chemistry
基金
上海市扬帆计划(No.15YF1403600)
国家自然科学基金(Nos.21602062
21373088
21425205)资助项目~~
