Synthesis of a tetracyclic lactam system of Nuevamine by four-component reaction and free radical cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. A new approach to isoindoloisoquinolinones. A simple synthesis of nuevamine
2. Construction of the Six- and Five-Membered Aza-Heterocyclic Units of the Isoindoloisoquinolone Nucleus by Parham-Type Cyclization Sequences -Total Synthesis of Nuevamine
3. A variation of the Pictet–Spengler reaction via a sequential reduction–cyclization reaction of N-acylcarbamates: synthesis of 1-substituted tetrahydroisoquinoline derivatives
4. Syntheses of Pyrrolo- and Indoloisoquinolinones by Intramolecular Cyclizations of 1-(2-Arylethyl)-5-benzotriazolylpyrrolidin-2-ones and 3-Benzotriazolyl-2-(2-arylethyl)-1-isoindolinones
5. Stereoselectivity of cyclisations via N-acyliminium ions to form pyrido[2′,3′:3,4]pyrrolo[2,1-a]isoindole, -isoquinoline and -benz[c]azepine ring systems
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