Two new entries to the ABF tricyclic ring system of 7,17-seco-type C19-diterpenoid alkaloids via free radical cyclization and [3+2] cycloaddition of nitrile oxide
Autor: | Liang Xu, Meng-Chen Liu, Yin-Juan Meng, Yong-Li Li |
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Rok vydání: | 2016 |
Předmět: |
Nitrile
010405 organic chemistry Stereochemistry Chemistry Organic Chemistry Oxide Total synthesis 010402 general chemistry Ring (chemistry) 01 natural sciences Biochemistry Radical cyclization Cycloaddition Terpenoid 0104 chemical sciences chemistry.chemical_compound Intramolecular force Drug Discovery |
Zdroj: | Tetrahedron. 72:3171-3176 |
ISSN: | 0040-4020 |
DOI: | 10.1016/j.tet.2016.04.027 |
Popis: | Two new approaches for the construction the ABF ring systems of 7,17-seco-type C19-diterpenoid alkaloids have been successfully developed by using free radical cyclization and intramolecular nitrile oxide cycloaddition, respectively, as the key steps. Both methods would probably provide alternative strategies for the elaboration of AEF-rings in the total synthesis of 7,17-seco-type C19-diterpenoid alkaloids based on our previously prepared BCD ring systems. |
Databáze: | OpenAIRE |
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