Carbocyclic Ring Construction via Intramolecular Ionic Diels−Alder Reactions of in Situ-Generated, Heteroatom-Stabilized Allyl Cations in Highly Polar Media
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (8) , 2095-2096
- https://doi.org/10.1021/ja9531992
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Acid catalyzed intramolecular Diels-Alder reactions in lithium perchlorate-diethyl ether: Acid promoted migration of terminal dienes prior to [4+2] cycloaddition in conformationally restricted substratesTetrahedron Letters, 1994
- Preparation of a Bicyclic Analog of Qinghao (Artemisinic) Acid via a Lewis Acid Catalyzed Ionic Diels-Alder Reaction Involving a Hydroxy Diene and Cyclic Enone and Facile Conversion into (.+-.)-6,9-DesdimethylqinghaosuThe Journal of Organic Chemistry, 1994
- Direct substitution of secondary allylic alcohols with O-silylated ketene acetals in 3.0 M lithium perchlorate-diethyl ether - An alternative to the [1,3] sigmatropic rearrangement of allyl vinyl ethersTetrahedron Letters, 1992
- Dramatic rate accelerations of Diels-Alder reactions in 5 M lithium perchlorate-diethyl ether: the cantharidin problem reexaminedJournal of the American Chemical Society, 1990
- Hydrofluoric acid catalyzed intramolecular Diels-Alder reactionsThe Journal of Organic Chemistry, 1984
- Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenonesThe Journal of Organic Chemistry, 1973