Diastereoselective and <i>E/Z</i>-Selective Synthesis of Functionalized Quinolizine Scaffolds via the Dearomative Annulation of 2-Pyridylacetates with Nitroenynes-Reference-Cited by-同舟云学术

Diastereoselective and E/Z-Selective Synthesis of Functionalized Quinolizine Scaffolds via the Dearomative Annulation of 2-Pyridylacetates with Nitroenynes

Published:2022-07-08 Issue:15 Volume:87 Page:9507-9517
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ni Qijian¹^ORCID,Xu Fangfang¹,Song Xiaoxiao¹

Affiliation:

1. Key Laboratory of Functionalized Molecular Solids, Ministry of Education, Anhui Key Laboratory of Molecule-Based Materials (State Key Laboratory Cultivation Base), College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241002, P. R. China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00448

Reference43 articles.

1. The quinolizine alkaloids

2. Indolizidine and quinolizidine alkaloids

3. Indolizidine and quinolizidine alkaloids

4. Cyclohexane-Fused Octahydroquinolizine Alkaloids from Myrioneuron faberi with Activity against Hepatitis C Virus

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