Control of the ring selectivity in Diels-Alder reactions of naphthazarins mediated by sulfur functions
- 30 May 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (22) , 3789-3792
- https://doi.org/10.1016/s0040-4039(00)73100-5
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Benzyl methyl (S)-2-(p-tolylsulfinyl)maleate: an efficient dienophile for the enantioselective synthesis of cyclohexadienesThe Journal of Organic Chemistry, 1993
- Directable regiochemistry in naphthazarins via the use of masked derivativesTetrahedron Letters, 1993
- Asymmetric Diels-Alder reactions of (S)-2-(p-tolylsulfinyl)-1,4-naphthoquinonesThe Journal of Organic Chemistry, 1992
- Synthesis of Optically Activep-TolylsulfinylquinonesSynthesis, 1992
- General synthesis of chiral 2-p-tolylsulfinylquinones.Tetrahedron, 1991
- Synthesis of anthracyclinones by electrophilic and nucleophilic addition to anthraquinonesTetrahedron, 1990
- Synthesis and asymmetric diels-alder reactions of (S)-2-p-tolylsulfinyl-1,4-benzoquinoneTetrahedron Letters, 1989
- Efficient, regiospecific synthesis of (.+-.)-daunomycinoneJournal of the American Chemical Society, 1980
- Regiochemical control in the Diels-Alder reactions of substituted naphthoquinones. Model studies on a regiospecific approach to adriamycinoneJournal of the American Chemical Society, 1977
- A novel route to tetracyclic hydroxyquinonesTetrahedron Letters, 1972