174591-33-4Relevant articles and documents
High-pressure and thermally induced asymmetric Diels-Alder cycloadditions of heterosubstituted dienes to homochiral α,β-didehydro amino acid derivatives
Ortuno, Rosa M.,Ibarzo, Javier,D'Angelo, Jean,Dumas, Francoise,Alvarez-Larena, Angel,Piniella, Joan F.
, p. 127 - 138 (1996)
An amino pentenoate and an unsaturated oxazolone have shown to be suitable homochiral dienophiles to be reacted with electron-rich heterosubstituted dienes. High-pressure and thermal activation have been studied for these cycloadditions. The adducts obtained are polyfunctional building blocks useful for the synthesis of enantiopure cyclohexane amino acids and related products.