articleJournal of the American Chemical SocietyJan 28, 2025Closed access

Enantioselective Synthesis of Tetrahydro-1 H -1,3-methanocarbazoles by Formal (3 + 3)-Cycloaddition Using Bicyclo[1.1.0]butanes

University of Münster

PubMed
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Abstract

Asymmetric synthesis presents many challenges, with the selective formation of chiral bridged polyheterocycles being a notable example. Cycloadditions using bicyclo[1.1.0]butanes (BCB) offer a promising solution along those lines, yet, despite significant advances in that emerging area, asymmetric control has remained limited thus far. Here, we describe an organocatalytic, enantioselective formal (3 + 3)-cycloaddition of BCBs with 1H-indol-3-yl((hetero)aryl)methanol derivatives. This approach enables the rapid and efficient synthesis of chiral tetrahydro-1H-1,3-methanocarbazole derivatives (34 examples) from readily available starting materials, with very good stereochemical control (up to 98:2 er). Successful…

Citation impact

56
total citations
FWCI
40.32
Percentile
100%
References
65
Citations per year

Authors

4

Topics & keywords

Keywords
  • Chemistry
  • Bicyclic molecule
  • Enantioselective synthesis
  • Cycloaddition
  • Formal synthesis
  • Stereochemistry
  • Organic chemistry
  • Catalysis
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