Formal [4+2] cycloaddition of quinolines, pyridines, and isoquinolines with 3-ethoxycyclobutanones
Author:
Funder
JSPS KAKENHI
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. 1.4‐Dipolare Cycloadditionen, II. Dreikomponenten‐Reaktionen des Isochinolins mit Acetylendicarbonsäureester und verschiedenen Dipolarophilen
2. A novel pyridine-based three-component condensation reaction: synthesis of highly substituted quinolizines
3. An Approach to the Synthesis of Spiro[indene-pyridoisoquinoline] Derivativesvia1,4-Dipolar Cycloaddition of Isoquinoline and Acetylene Esters, and (1,3-Dihydro-1,3-dioxo-2H-inden-2-ylidene)malononitrile
4. Construction of heterocycles via 1,4-dipolar cycloaddition of quinoline–DMAD zwitterion with various dipolarophiles
5. The reaction of isoquinoline and dimethyl acetylenedicarboxylate with 1,2- and 1,4-benzoquinones: a novel synthesis of spiro[1,3]oxazino[2,3-a]isoquinolines
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1. Bicyclic 6-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: No Extra Heteroatom;Comprehensive Heterocyclic Chemistry IV;2022
2. Lewis Acid Catalyzed Ring‐Opening Reaction of Cyclobutanones towards Conjugated Enones;European Journal of Organic Chemistry;2021-12-02
3. A Solvent‐free, Catalyst‐free Formal [3+3] Cycloaddition Dearomatization Strategy: Towards New Fluorophores for Biomolecules Labelling;ChemSusChem;2021-03-15
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