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Can I read Chiral butenolides as dienophiles in Diels-Alder cycloadditions on EtoBox?
Chiral butenolides as dienophiles in Diels-Alder cycloadditions by R.M. Ortuño; J. Corbera; J. Font is a Chemistry article available to read on EtoBox.
What is Chiral butenolides as dienophiles in Diels-Alder cycloadditions about?
Differently substituted chiral butenolides, prepared from D-ribonolactone react atadiene at 210" affording enantiomerically pure bicycloadducti as single dialtereoisomers, in good yields. The ability of protoanemonin (formed in some pyrolytic reaction conditions) to react regiospecifically at the exocyclic double bond, to give spirolactones, isshown. The Diels-Alder cycloaddition remains today one of the most powerful synthetic methods.
Who reads Chiral butenolides as dienophiles in Diels-Alder cycloadditions?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- R.M. Ortuño; J. Corbera; J. Font
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
- Published
- 1986
- Language
- EN
- Field
- Chemistry (Physical Sciences)