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Updated: Mar 30, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
A Domino Diels-Alder Approach toward the Tetracyclic Nicandrenone Framework
Emily G Mackay1, Marck Nörret1, Leon S-M Wong1
1Research School of Chemistry, Australian National University , Canberra, ACT 2601, Australia.
Abstract:
The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a linear precursor via a domino intramolecular Diels-Alder/intramolecular furan Diels-Alder/aromatization sequence. The approach represents a new 0 → ABCD strategy for the preparation of aromatic steroids.
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