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December 5, 2025Advanced Synthesis & Catalysis1 citations

Stereoselective De Novo Synthesis of Substituted Cyclopentanes via a Gold(I)‐Catalyzed (3 + 2) Cycloaddition of Enamides

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AAAmjad Ayad Qatran Al‐KhdhairawiTYTengrui YuanKHKristof Van Hecke

Key Points

  • Synthesis enhances reactivity in the formation of substituted cyclopentanes using enamides, with significant results on selectivity.
  • The cycloaddition reaction yields cyclopentylamine scaffolds by employing an aurated dithioallyl cation as a key intermediate.
  • Analysis shows a classical stepwise (3 + 2) mechanism, highlighting the unique role of the gold(I) catalyst in directing the reaction.
  • Reactivity and chemoselectivity are influenced by counterion effects, suggesting pathways for optimizing similar reactions.

Abstract

A general and stereoselective synthesis of highly substituted cyclopentylamine scaffolds is reported starting from various N‐alkenyl‐amides. The reaction involves the generation of an aurated dithioallyl cation which undergoes a classical stepwise (3 + 2) allyl cation cycloaddition with a range of enamide substrates. The close coordination of the reactive intermediates with the well‐defined gold(I)‐catalyst results in a reactivity and selectivity profile that can be readily rationalized on the basis of a nonconcerted carbocationic cycloaddition reaction, and some remarkable counterion effects are seen to effect the chemoselectivity of the overall process.

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Cite This Study

Al‐Khdhairawi et al. (2025) studied this question.

synapsesocial.com/papers/6940224e2d562116f28fc1d3https://doi.org/10.1002/adsc.70182
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