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April 27, 2026Angewandte Chemie International Edition1 citations

Enantioselective Synthesis of Inherently Chiral Tetraphenylene Analogues Enabled by NHC‐Catalyzed Benzoin Condensation

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YZYuanhang ZhangYLYu LuoTZTao Zhang

Key Points

  • This research aims to develop an enantioselective method for synthesizing inherently chiral tetraphenylene analogues.
  • NHC-catalyzed benzoin reaction of bisaldehydes
  • Synthesis of eight-membered α-hydroxy ketones
  • DFT calculations to analyze reaction mechanisms
  • Successfully synthesized a variety of chiral tetraphenylene analogues.
  • Demonstrated a saddle-shaped conformation in the resulting compounds.
  • Provided mechanistic insights into the stereoselectivity via DFT analysis.

Abstract

ABSTRACT Herein, we report an enantioselective N‐heterocyclic carbene (NHC)‐catalyzed intramolecular benzoin reaction of bisaldehydes featuring a 1,1′:2′,1′′‐terphenyl linkage to afford eight‐membered α‐hydroxy ketones in which six of the eight ring atoms are benzene carbons. The benzene‐rich framework is conformationally inflexible and thus inherently chiral, adopting a saddle‐shaped conformation. A variety of heteroaromatic‐ and naphthalene‐embedded tetraphenylene analogues were prepared enantioselectively by routine transformations of the α‐hydroxy ketone moiety. Density functional theory (DFT) calculations elucidate the reaction mechanism and provide insights into the origin of the stereoselectivity.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/69eefd15fede9185760d3e00https://doi.org/10.1002/anie.6712761
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