ArticleAngewandte Chemie (International ed. in English)2018
Development of the Vinylogous Pictet-Spengler Cyclization and Total Synthesis of (±)-Lundurine A.
Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Asymmetric Synthesis of the Pentacyclic Framework ofOrganic letters · 2025Article
- C-H functionalization of 2-alkyl tryptamines: direct assembly of azepino[4,5-Chemical science · 2024Article
- Microwave-AssistedACS omega · 2018Article
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Authors and funding
5 authors.
Funding
Abstract
A novel vinylogous Pictet-Spengler cyclization has been developed for the generation of indole-annulated medium-sized rings. The method enables the synthesis of tetrahydroazocinoindoles with a fully substituted carbon center, a prevalent structural motif in many biologically active alkaloids. The strategy has been applied to the total synthesis of (±)-lundurine A.
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Registered trials
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