A new form of secondary interaction in diels-alder reactions

Autor: Raifel'd, Yu. E., Él'yanov, B. S., Makin, S. M.
Zdroj: Russian Chemical Bulletin; May 1976, Vol. 25 Issue: 5 p1058-1061, 4p
Abstrakt: 1.The diene condensation of 1-alkoxy-1,3-butadienes with aliphatic aldehydes at high pressures leads to predominate formation of 2-alkoxy-6-alkyl-?3-dihydropyrans, corresponding to the endo-orientation of the diene and dienophile in the transition state.2.The observed effect is explained by the presence of interaction of the partially protonated hydrogen on the a-carbon atom of the aldehyde with the p-system of the diene.
Databáze: Supplemental Index