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Intramolecular reactions of allyloxy radicals

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Date

1989

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Abstract

Allyloxy radicals, formed by epoxide cleavage, have cyclised onto appropriately positioned alkenes to form tetrahydrofurans, and the diastereoselectivity of the cyclisation has been studied. The reaction was used to synthesise lilac alcohols which were then used to confirm the stereochemistry of such cyclisations.

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Citation

URI

https://dspace-test.anu.edu.au/handle/1885/733744757

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DevOps Pure Testing

Source

Tetrahedron

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Article

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DOI

10.1016/S0040-4020(01)85798-7

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