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Updated: Aug 18, 2025

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Brønsted acid-catalysed desilylative heterocyclisation to form substituted furans
Emily G Babcock1, Md Shafiqur Rahman1, James E Taylor1
1Department of Chemistry, University of Bath, Claverton Down, Bath, Somerset, BA2 7AY, UK. jet21@bath.ac.uk.
Abstract:
Heterocyclisation of tert-butyldimethylsilyl (TBS) protected γ-hydroxy-α,β-unsaturated ketones catalysed by para-toluenesulfonic acid (p-TSA) to form substituted furans is reported. The reaction proceeds under mild conditions at room temperature in methanol to give a range of furan products (21 examples, up to 98% yield). Mechanistic experiments suggest the reaction proceeds via in situ deprotection followed by catalytic dehydrative heterocyclisation.
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