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Novel Reaction Pathways for 2-Pyridone [4+4] Photoadducts

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Novel_Reaction_Pathways_for_2_Pyridone_4_4_Photoadducts/3070021
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Transannular ring closure of a pyridone−furan [4+4] photoadduct has been evaluated in a model system. A combination of nitrogen substitution and an isopropyl group gave full control of the four new stereogenic centers. Chlorination transformed the 1,5-cyclooctadiene to a [4.2.0] ring system instead of to the expected [3.3.0] ring system. Changing an alkene to an enone suppressed this pathway and led to a new rearrangement, converting the 5-8-5 ring system to a 6-7-5 system.
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2016-03-01
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