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Indexed by:期刊论文
Date of Publication:2018-01-01
Journal:The Journal of organic chemistry
Included Journals:PubMed、SCIE、Scopus
Volume:83
Issue:9
Page Number:5044-5051
ISSN No.:1520-6904
Abstract:A stereoselective sequential [4+2]/[2+2] cycloaddition process involving 2-alkenylindolenines has been developed. This unprecedented protocol allows a rapid access to densely functionalized benzo[ b]indolizidines containing a fully substituted piperidine ring with five contiguous stereogenic centers in good yields with excellent diastereoselectivities. This finding demonstrated the unique synthetic utility of the 2-alkenylindolenine species in the construction of complex polycyclic N-heterocycles.