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An asymmetric route to fused carbocyclic systems via Diels-Alder reactions on chiral α,β-unsaturated bicyclic lactams by A.I. Meyers; Carl A. Busacca is a Chemistry article available to read on EtoBox.

What is An asymmetric route to fused carbocyclic systems via Diels-Alder reactions on chiral α,β-unsaturated bicyclic lactams about?

The cycloadducts from Diels-Alder reactions have been transformed into novel functionalized carbocycles 11 and 12 in high enantiomeric excess. In the previous Letter,' we have described the efficient cycloaddition of various dienes to the chiral, non-racemic lactam 1. We now wish to describe the utility of these cycloadducts in providing novel and interesting fused carbocycles in high enantiomeric purity. Two dienes, isoprene and myrcene, were chosen as examples to demonstrate the potential

Who reads An asymmetric route to fused carbocyclic systems via Diels-Alder reactions on chiral α,β-unsaturated bicyclic lactams?

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Author
A.I. Meyers; Carl A. Busacca
Publisher
Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
Published
1989
Language
EN
Field
Chemistry (Physical Sciences)

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