Abstract

Higher-order cycloadditions are a powerful strategy for the construction of polycycles in one step. However, an efficient and concise version for the induction of asymmetry is lacking. N-heterocyclic carbenes are widely used organocatalysts for asymmetric synthesis and could be an ideal choice for enantioselective higher-order cycloadditions. Here, we report an enantioselective [10 + 2] annulation between catalytically formed aza-benzofulvene intermediates and trifluoromethyl ketone derivatives. This protocol exhibits a wide scope, high yields, and good ee values, reflecting a robust and efficient higher-order cycloaddition. Density functional theory calculations provide an accurate prediction of the reaction enantioselectivity, and in-depth insight to the origins of stereocontrol.

Highlights

  • Higher-order cycloadditions are a powerful strategy for the construction of polycycles in one step

  • The enantioselective [2 + 3] cycloaddition of enolates with oxaziridines or nitrovinylindoles has been reported by Shao et al.[21] and Ni et al.[22] groups, using N-heterocyclic carbenes (NHCs) organocatalysis, independently

  • A recent Chen et al.[60] work indicated that salicylaldehydes could be oxidized to generate NHCbounded o-quinone methide intermediates (8π-electron), which participated in a [8 + 2] cycloaddition with electrophile trifluoromethyl ketones

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Summary

Introduction

Higher-order cycloadditions are a powerful strategy for the construction of polycycles in one step. Normal order cycloadditions (cycloaddition that involves

Results
Conclusion

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