Gold(Ⅰ)-Catalyzed Diastereo- and Enantioselective Synthesis of Polysubstituted Pyrrolo[3,4-d][1,2 ]oxazines
Gold(Ⅰ)-Catalyzed Diastereo- and Enantioselective Synthesis of Polysubstituted Pyrrolo[3,4-d][1,2 ]oxazines作者机构:Shanghai Key Laboratory of Green Chemistry and Chemical Processes Department of Chemistry East China Normal University 3663 N Zhongshan Road Shanghai 200062 China State Key Laboratory of Organometallic Chemistry Shanghai Institute of Organic Chemistry Chinese Academy of Sciences Shanghai 200032 China
出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))
年 卷 期:2018年第36卷第6期
页 面:519-525页
核心收录:
学科分类:081704[工学-应用化学] 081705[工学-工业催化] 07[理学] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学] 070301[理学-无机化学]
基 金:We are grateful to the National Natural Science Foundation of China (21425205) Ministry of Education of China Ying Tung Education Foundation (121014) for financial support
主 题:gold(Ⅰ)-catalysis heterobicyclic pyrroles oxime ethers nitrones tandem reaction
摘 要:A gold(I)-catalyzed highly diastereo- and enantioselective intermolecular cycloaddition of oxime ethers with nitrones under mild conditions was developed, which provides an facile access to optically pure highly substituted pyrrolo[3,4-d][1,2]oxazines. The salient features of this reaction in- clude general substrate scope, high efficiency, high enantioselectivity, readily available starting materials, and the use of commercially available ligand.