97253-95-7Relevant academic research and scientific papers
2,4-Cyclohexadien-1-ones in Organic Synthesis. Intramolecular Diels-Alder Reactivity and the Oxa-di-?-methane Photorearrangement of Diels-Alder Adducts
Schultz, Arthur G.,Lavieri, Frank P.,Snead, Thomas E.
, p. 3086 - 3091 (2007/10/02)
The preparation and intramolecular Diels-Alder reactions of a series of 6-alkenyl-6-(methoxycarbonyl)2,4-cyclohexadien-1-ones are described.The resulting tricyclic β,γ-enones undergo the oxa-di-?-methane rearrangement to give substrates of potential use in the construction of polyquinane natural products.This methodology provides a means for construction of tetracyclic rings of type A by C-alkylation of the synthetic equivalence of enolate B.
