Interaction | Reaction | Process     Data Page

In this Diels-Alder cycloaddition both the diene and dieneophile are electron rich. As a result there is a small LUMO/HOMO energy gap and the reaction is slow.

Reactant Page Go To Go To
Butadiene, 1,3-methoxy     Reactions Using    Reactions Forming
1,1-Diethoxyethene     Reactions Using    Reactions Forming
3-Methoxy-4,4- diethoxy cyclohexene     Reactions Using    Reactions Forming

Interaction, Reaction, Process defined as:
Diels-Alder (type) Cycloaddition
Type 20 Lewis Acid/Base Complexation Chemistry

© Mark R. Leach 1999 –

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