Acid-Promoted Aza-Cyclization versus π-Cyclization of N-Acyliminium Species into Fused Pyrrolo[1,2-a]imidazolones and Pyrrolo[2,1-a]isoquinolinones
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1260949.pdf
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Aza-heterocyclic frameworks through intramolecular π-system trapping of spiro-N-acyliminiums generated from isoindolinone;New Journal of Chemistry;2021
2. In-depth examination of the pterolactams behaviour in Lewis/Brönsted acid catalysis environment: Total isolation of the reaction products;Arkivoc;2020-11-30
3. Benzo[7,8]indolizinoquinoline scaffolds based on Mg(ClO4)2-promoted regiospecific imide reduction and π-cyclization of N-acyliminium species. Analogues of the topo-1 poison rosettacin and 22-hydroxyacuminatine alkaloids;Arabian Journal of Chemistry;2019-07
4. 1,3,5-Oxadiazine Framework by Oxygen vs. Nitrogen Trapping of anN-Acyliminium Ion Derived fromN,O-bis-TMS Pyroglutamic Acid;ChemistrySelect;2017-11-21
5. Controllable Diastereodivergent Synthesis of Pyrrolo[2,1-a]isoquinolines via Catalytic Intramolecular Acylsulfenylation of Activated Alkenes;The Journal of Organic Chemistry;2017-04-25
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