{"title":"Modular Strategy for the Collective Total Synthesis of Pandanus amaryllifolius Alkaloids: Pandanusines A and B and Pandamarine","authors":"Edouard Fauran, Jean-Valère Naubron, Laurent Commeiras","doi":"10.1021/acs.joc.6c01791","DOIUrl":null,"url":null,"abstract":"<p><em>Pandanus amaryllifolius</em> produces structurally\r\nunique alkaloids, including pandanusines A and B and pandamarine,\r\nfeaturing rare diazaspirocyclic γ-lactam frameworks. Herein,\r\nwe report concise total syntheses of these three natural products\r\nbased on a modular copper(I)-catalyzed reaction. Readily accessible\r\nγ-hydroxy-γ-lactams were prepared from iodoacrylic acids,\r\nterminal alkynes, and primary amines and subsequently transformed\r\nthrough <em>N</em>-acyliminium ion intermediates to construct\r\ndiazaspirocyclic backbones. This strategy enabled the synthesis of\r\n(±)-pandanusine B in four steps (40% overall yield) and (±)-pandanusine\r\nA in five steps (26.5% overall yield) after optimization of the protecting\r\ngroup strategy. The methodology was further extended to the total\r\nsynthesis of the more complex alkaloid pandamarine. These results\r\ndemonstrate the synthetic potential of γ-hydroxy-γ-lactams\r\nas versatile precursors for the rapid construction of architecturally\r\ncomplex alkaloid scaffolds. Furthermore, the absolute configurations\r\nof both HPLC-separated enantiomers of pandanusine A and B were unambiguously\r\ndetermined through a combination of vibrational and electronic circular\r\ndichroism analyses and DFT and TD-DFT calculations.</p>","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"91 41","pages":"13724–13734"},"PeriodicalIF":3.3000,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.6c01791","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/30 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Pandanus amaryllifolius produces structurally
unique alkaloids, including pandanusines A and B and pandamarine,
featuring rare diazaspirocyclic γ-lactam frameworks. Herein,
we report concise total syntheses of these three natural products
based on a modular copper(I)-catalyzed reaction. Readily accessible
γ-hydroxy-γ-lactams were prepared from iodoacrylic acids,
terminal alkynes, and primary amines and subsequently transformed
through N-acyliminium ion intermediates to construct
diazaspirocyclic backbones. This strategy enabled the synthesis of
(±)-pandanusine B in four steps (40% overall yield) and (±)-pandanusine
A in five steps (26.5% overall yield) after optimization of the protecting
group strategy. The methodology was further extended to the total
synthesis of the more complex alkaloid pandamarine. These results
demonstrate the synthetic potential of γ-hydroxy-γ-lactams
as versatile precursors for the rapid construction of architecturally
complex alkaloid scaffolds. Furthermore, the absolute configurations
of both HPLC-separated enantiomers of pandanusine A and B were unambiguously
determined through a combination of vibrational and electronic circular
dichroism analyses and DFT and TD-DFT calculations.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.