128374-25-4Relevant academic research and scientific papers
An asymmetric route to fused carbocyclic systems via Diels-Alder reactions on chiral α,β-unsaturated bicyclic lactams
Meyers,Busacca
, p. 6977 - 6980 (1989)
The cycloadducts from Diels-Alder reactions have been transformed into novel functionalized carbocycles 11 and 12 in high enantiomeric excess.
Asymmetric Diels-Alder Reactions. A Route to Chiral Carbocycles via Bicyclic Lactams
Busacca, Carl A.,Meyers, A. I.
, p. 2299 - 2316 (2007/10/02)
The L-valinol-derived unsaturated lactam methyl 3-isopropyl-7a-methyl-5-oxo-2,3-dihydro-7aH-pyrrolooxazole-6-carboxylate functions as an excellent chiral dienophile in asymmetric Diels-Alder reactions.Diene approach occurs exclusively from the α-(e
