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Regio- and Diastereoselective Stepwise [8 + 3]-Cycloaddition Reaction between Tropone Derivatives and Donor–Acceptor Cyclopropanes

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NIAID Data Ecosystem2026-03-07 收录
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A novel SnCl4-catalyzed [8 + 3]-cycloaddition reaction between tropone derivatives and donor–acceptor aminocyclopropanes is described. The process leads to the formation of amino-substituted tetrahydrocyclohepta[b]pyrans with complete regio- and diastereoselectivity. Density functional theory calculations suggest that the cycloaddition occurs stepwise through an aromatic zwitterionic intermediate.

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2013-10-04
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