Last Updated:2025/11/25

The exo-isomer of the bridged bicyclic compound was more reactive in Diels–Alder reactions because its substituent is positioned farthest from the longest bridge.

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The exo-isomer of the bridged bicyclic compound was more reactive in Diels–Alder reactions because its substituent is positioned farthest from the longest bridge.

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その架橋二環化合物のエクソ異性体は、置換基が最長の橋から最も離れた位置にあるため、ディールス–アルダー反応でより反応性が高かった。

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