The Synthesis of Cyclopropyl‐Fused Tetrahydrofurans from Vinylcyclopropanes

Abstract The rapid synthesis of oxabicyclo[3.1.0]hexanols from various vinylcyclopropanes is described. Several carbonyl functionalities were incorporated, as were a range of electronically and sterically diverse aromatic and aliphatic substituents. This structurally unusual building block was then showcased through the rapid synthesis of a series of structurally complex polycyclic compounds.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-07-12
DOI
https://doi.org/10.1002/ajoc.70110
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

The Synthesis of Cyclopropyl‐Fused Tetrahydrofurans from Vinylcyclopropanes

Owain H. Harker, Sinan Gai, Jackson S. Henneveld, Bill C. Hawkins et al.
Asian Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
article

The Synthesis of Cyclopropyl‐Fused Tetrahydrofurans from Vinylcyclopropanes

Owain H. Harker, Sinan Gai, Jackson S. Henneveld, Bill C. Hawkins, Andrew P. Cording, Alexander J. Craig, Susan Gilmer, Nigel T. Lucas
article en

Abstract

Abstract The rapid synthesis of oxabicyclo[3.1.0]hexanols from various vinylcyclopropanes is described. Several carbonyl functionalities were incorporated, as were a range of electronically and sterically diverse aromatic and aliphatic substituents. This structurally unusual building block was then showcased through the rapid synthesis of a series of structurally complex polycyclic compounds.

Asian Journal of Organic ChemistryVol. 14(9)
University of Otago (NZ)
University of Otago
Openalex Percentile: Top 87%
Cyclopropane Reaction Mechanisms
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