Synthesis of heterobicyclo[ <i>n</i> .1.1]alkanes

Heterocyclic bicyclo[<i>n</i>.1.1]alkanes have emerged as important scaffolds in contemporary drug design due to their rigid frameworks that enable the positioning of their subsituents along well defined vectors in chemical space. Offering much potential as alternative cores to traditional benzene rings, heterobicyclo[2.1.1]hexanes (HBCHexs) and heterobicyclo[3.1.1]heptanes (HBCHeps) in particular have attracted significant attention from the synthetic community. A plethora of methods have recently been developed to access these useful motifs, using both radical and polar strategies to forge the bicyclic system. This review discusses recent developments in the field, with a focus on mechanistic aspects, and those methodologies that show the most potential for general application.

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Publication Details

Journal
Chemical Society Reviews
Published
2025-12-17
DOI
https://doi.org/10.1039/d5cs01128k
Citations
5
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
4.68

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article

Synthesis of heterobicyclo[ n .1.1]alkanes

Julia Ragus, Edward A. Anderson, Rebecca I. Revie
5 citations
Chemical Society Reviews
Radical Photochemical Reactions
4.68
article

Synthesis of heterobicyclo[ n .1.1]alkanes

Julia Ragus, Edward A. Anderson, Rebecca I. Revie
article en
5 citations

Abstract

Heterocyclic bicyclo[<i>n</i>.1.1]alkanes have emerged as important scaffolds in contemporary drug design due to their rigid frameworks that enable the positioning of their subsituents along well defined vectors in chemical space. Offering much potential as alternative cores to traditional benzene rings, heterobicyclo[2.1.1]hexanes (HBCHexs) and heterobicyclo[3.1.1]heptanes (HBCHeps) in particular have attracted significant attention from the synthetic community. A plethora of methods have recently been developed to access these useful motifs, using both radical and polar strategies to forge the bicyclic system. This review discusses recent developments in the field, with a focus on mechanistic aspects, and those methodologies that show the most potential for general application.

Chemical Society ReviewsVol. 55(2)
Mansfield University (US), University of Oxford (GB)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 5%
Radical Photochemical Reactions
4.68
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