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- W2050130410 endingPage "18842" @default.
- W2050130410 startingPage "18834" @default.
- W2050130410 abstract "The pyrrole–imidazole alkaloids have fascinated chemists for decades because of their unique structures. The high nitrogen and halogen contents and the densely functionalized skeletons make their laboratory synthesis challenging. We describe herein an oxidative method for accessing the core skeletons of two classes of pyrrole–imidazole dimers. This synthetic strategy was inspired by the putative biosynthesis pathways and its development was facilitated by computational studies. Using this method, we have successfully prepared ageliferin, bromoageliferin, and dibromoageliferin in their natural enantiomeric form." @default.
- W2050130410 created "2016-06-24" @default.
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- W2050130410 creator A5069002696 @default.
- W2050130410 date "2012-11-02" @default.
- W2050130410 modified "2023-10-07" @default.
- W2050130410 title "A Biomimetic Route for Construction of the [4+2] and [3+2] Core Skeletons of Dimeric Pyrrole–Imidazole Alkaloids and Asymmetric Synthesis of Ageliferins" @default.
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- W2050130410 doi "https://doi.org/10.1021/ja309172t" @default.
- W2050130410 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3498534" @default.
- W2050130410 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23072663" @default.
- W2050130410 hasPublicationYear "2012" @default.