| Literature DB >> 27599657 |
Jin-Hui Xu1, Sheng-Cai Zheng1, Ji-Wei Zhang1, Xin-Yuan Liu1, Bin Tan2.
Abstract
A chiral-NHC-catalyzed highly diastereo- and enantioselective dearomatizing double Mannich reaction of isoquinolines was developed that provides a powerful and straightforward synthetic route toward substituted tropane derivatives with four contiguous stereocenters. A unique feature of this strategy is the use of readily available isoquinolines to provide two reactive sites for dearomatization, thus opening up an unprecedented approach to tropane derivatives with excellent stereoselectivity. The four-component reactions proceeded smoothly with good results. Thus, the present method is suitable for the diversity-oriented synthesis of useful tropane derivatives with high efficiency.Entities:
Keywords: N-heterocyclic carbenes; asymmetric catalysis; dearomatization; isoquinolines; tropanes
Year: 2016 PMID: 27599657 DOI: 10.1002/anie.201605736
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336