An efficient entry to highly functionalised C4chiral synthons via Lewis acid-catalysed ene reaction of (1S)-β-pinene and α-keto esters. Part 4.
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900001875
Reference31 articles.
1. Monoterpenoid chemistry. Part 3.. Stereoselective synthesis of the major oxygenated metabolites oftrans-sobrerol
2. Lewis-acid catalyzed ene reactions
3. Intramolecular Ene Reactions in Organic Synthesis
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3. ChemInform Abstract: An Efficient Entry to Highly Functionalised C4 Chiral Synthons via Lewis Acid-Catalysed Ene Reaction of (1S)-β-Pinene and α-Keto Esters. Part 4.;ChemInform;1990-10-23
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