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- W2130450496 abstract "One-of-a-kind. A bromine-induced rearrangement has been designed for the formation of the spiro-β-lactam ring present in the structurally unique chartelline alkaloids (see picture of chartelline A). This method is used in combination with others to provide rapid access to the carbocyclic skeletons of the chartelline, securine, and securamine alkaloids. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2005/z500522_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2130450496 date "2005-06-06" @default.
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- W2130450496 title "A Remarkable Ring Contraction En Route to the Chartelline Alkaloids" @default.
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- W2130450496 doi "https://doi.org/10.1002/anie.200500522" @default.
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