Synthetic approach to aklavinone using 2-oxo-2H-pyran-5-carboxylate (coumalate) intermediates
- 1 May 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (10) , 1889-1902
- https://doi.org/10.1021/jo00386a002
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Regiospecific total synthesis of juncusolThe Journal of Organic Chemistry, 1984
- Regiospecific synthesis of mono- and bicyclic 6-alkoxy-2-pyrones and their use in the preparation of substituted aromatics, anthraquinones, and tetracyclic intermediates for 11-deoxyanthracycline synthesisTetrahedron, 1984
- Pyranonaphthoquinone antibiotics. 4. Total synthesis of (+)-griseusin A, an enantiomer of the naturally occurring griseusin AThe Journal of Organic Chemistry, 1983
- Synthetic approaches to aclacinomycin and pyrromycin antitumour antibiotics via Diels–Alder reactions of 6-alkoxy-2-pyrones: total synthesis of chrysophanol, helminthosporin and pachybasinJournal of the Chemical Society, Chemical Communications, 1978
- New anthracycline antibiotics, rhodirubins.The Journal of Antibiotics, 1977
- Structure of nogalamycinJournal of the American Chemical Society, 1977