Domino-Like Ring Expansion

  • ChemPubSoc Europe Logo
  • Author: Chemistry – A European Journal
  • Published Date: 04 February 2018
  • Source / Publisher: Chemistry – A European Journal/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: Domino-Like Ring Expansion

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How can a lactone be prepared without a lactonization step? There are many creative answers to this question. The ring expansion of 1,3-cyclohexanedione is one example, but so far, 9-membered lactones have been difficult to obtain because of strain within the framework.

Michaël De Paolis, Normandie Université, Rouen, France, and colleagues have discovered a route to 9-membered lactones. The team used an anionic fragmentation of 2-nitrophenyl-1,3-cyclohexanediones which contain an electrophilic appendage such as an aldehyde or an epoxide (pictured). The reaction is initiated by a nucleophile. The mechanism proceeds in a domino-like fashion. The negative charge brought by the nucleophile is transferred from one heteroatom to a remote heteroatom, thus provoking the ring expansion.

This strategy provides access to lactones with a fused indole unit and a range of functional groups (alkyne, alkene, ester, nitrile, bromide, and azide). As they are relatively rigid and large, these lactones may interact with biological hosts. Since natural products combining medium-sized lactone and indole motifs are rather uncommon, this combination of the two is expected to be of interest in the molecular biosciences.


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