Intramolecular diels-alder cycloadditions of substituted furfuryl E-2-(phenylsulfonyl)acrylates
Some substituted furfuryl E-2-(phenylsulfonyl)acrylates 7 have been prepared from the furfuryl alcohols 5 & the acid chloride 6 and cyclized in good yield under very mild conditions, e.g., 2h at 25°C, to give highly oxidized systems 9 of potential use in natural products synthesis.
References (17)
- et al.
Tetrahedron Lett.
(1973)Phosphorus Sulfur
(1985)Chem. Ind.
(1981)et al.J. Chem. Soc.
(1983) - et al.
Nat. Prod. Rep.
(1986)et al. Parasitol. Today
(1985)et al.J. Vet. Pharmacol. Ther.
(1983)et al.Experientia
(1981)- et al.
Brit. J. Ophthalmol.
(1987) - et al.
J. Am. Chem. Soc.
(1987)et al.J. Am. Chem. Soc.
(1987)et al.J. Am. Chem. Soc.
(1987)et al.J. Org. Chem.
(1988)et al.J. Org. Chem.
(1988)et al.J. Org. Chem.
(1988)et al.Tetrahedron Lett.
(1988)et al.Tetrahedron Lett.
(1987)i)For earlier synthetic work, see list of references in... - et al.
Heterocycles
(1988)et al.Tetrahedron Lett.
(1985)et al.J. Am. Chem. Soc.
(1984)
There are more references available in the full text version of this article.
Cited by (0)
- 1
UCLA Gold Shield Faculty Awardee, 1986–1988.
Copyright © 1988 Published by Elsevier Ltd.