Imidazole-catalyzed construction of bridged bicyclo [3.3.1] ketals via formal [3 + 3]-cycloaddition of naphthols and 2-hydroxyl chromene derivatives

Abstract

Bridged bicyclo[3.3.1]nonanes having the O,O-ketal subunit are widely found in medicinal compounds. While several acid-catalyzed approaches have been reported for the construction of ketals, this study discloses an imidazole-catalyzed modular construction of bicyclo[3.3.1]nonanes from naphthols/phenols and 3-acyl-2-hydroxyl chromenes. The proposed reaction pathway follows a formal [3 + 3] cycloaddition of phenols and an oxonium dipolar intermediate. The reaction is efficient regarding scalability, environmentally benign conditions, and resulting in the products in good to excellent yields.

Graphical abstract: Imidazole-catalyzed construction of bridged bicyclo [3.3.1] ketals via formal [3 + 3]-cycloaddition of naphthols and 2-hydroxyl chromene derivatives

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Article information

Article type
Communication
Submitted
21 Dec 2024
Accepted
10 Feb 2025
First published
10 Feb 2025

Org. Biomol. Chem., 2025, Advance Article

Imidazole-catalyzed construction of bridged bicyclo [3.3.1] ketals via formal [3 + 3]-cycloaddition of naphthols and 2-hydroxyl chromene derivatives

A. Budakoti, P. Jha, M. Verma, P. G. Vasudev and A. Gupta, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D4OB02068E

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