Computational and Experimental Investigation of the Diels−Alder Cycloadditions of 4-Chloro-2(H)-pyran-2-one
Author:
Affiliation:
1. Department of Chemistry, King's College, Strand, London WC2R 2LS, UK
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0348827
Reference31 articles.
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2. Recent advances in diels-alder cycloadditions of 2-pyrones
3. Lewis acid-catalyzed, high pressure, stereospecific, regiospecific, Diels-Alder cycloaddition of unsubstituted 2-pyrone: Short synthesis of a racemic A-ring precursor to physiologically active 1-hydroxyvitamin D3 steroids
4. Tandem pericyclic reactions. The first X-Ray structure of an initial pyrone-olefin adduct and an easy, stereocontrolled, entry into polyoxygenated cyclohexanes
5. Asymmetric Diels-Alder cycloadditions using chiral alkyl vinyl ethers and a dienyl sulfone
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