16.21:
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
16.21:
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Un abonnement à JoVE est nécessaire pour voir ce contenu. Connectez-vous ou commencez votre essai gratuit.
3,215 Views
•
00:00 min
•
April 30, 2023
Diels–Alder reactions between cyclic dienes locked in an s-cis configuration and dienophiles yield bridged bicyclic products.
Dienophiles with one or more electron-withdrawing substituents form stereochemically different products in which the substituents are oriented in an endo (towards) or exo (away) configuration relative to the double bond.
The endo isomer is formed faster and is the kinetic product. The exo isomer is more stable and is the thermodynamic product.