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ChemInform Abstract: An Unusual Michael‐Induced Skeletal Rearrangement of a Bicyclo[3.3.1]nonane Framework of Phloroglucinols to a Novel Bioactive Bicyclo[3.3.0]octane.

Veroniki P. Vidali, Kornilia P. Mitsopoulou, Marianna Dakanali, Konstantinos D. Demadis, Andreani D. Odysseos, Yiota A. Christou, Elias A. Couladouros

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Abstract

Abstract The reactivity of the Δ7,10‐double bond of bicyclic[3.3.1]nonatriones such as (I) is investigated resulting in the discovery of a novel skeletal rearrangement to a highly functionalized bicyclo[3.3.0]octane.

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What this paper is about

Abstract The reactivity of the Δ7,10‐double bond of bicyclic[3.3.1]nonatriones such as (I) is investigated resulting in the discovery of a novel skeletal rearrangement to a highly functionalized bicyclo[3.3.0]octane.

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Available abstract

Abstract The reactivity of the Δ7,10‐double bond of bicyclic[3.3.1]nonatriones such as (I) is investigated resulting in the discovery of a novel skeletal rearrangement to a highly functionalized bicyclo[3.3.0]octane.

Key concepts: Bicyclic molecule, Chemistry, Octane, Nonane, Bridged compounds, Reactivity (psychology), Stereochemistry, Medicinal chemistry

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ChemInform Abstract: An Unusual Michael‐Induced Skeletal Rearrangement of a Bicyclo[3.3.1]nonane Framework of Phloroglucinols to a Novel Bioactive Bicyclo[3.3.0]octane. — Research Paper | ScholarLens