A convergent rgiospecific route to the aklavinone ring system
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (38), 3741-3744
- https://doi.org/10.1016/s0040-4039(01)82008-6
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- A regiospecific synthesis of (±)-decarbomethoxyaklavinoneTetrahedron Letters, 1981
- Anthracyclines. II - regiospecific synthesis of 6-deoxyanthracycline intermediatesTetrahedron Letters, 1981
- The vinylketene acetal route to aklavinone and 11-deoxydaunomycinoneTetrahedron Letters, 1980
- A general route to 11-deoxyanthracyclinesTetrahedron Letters, 1980
- Antitumor agents from the bohemic acid complex. 4. Structures of rudolphomycin, mimimycin, collinemycin, and alcindoromycinJournal of the American Chemical Society, 1979
- Regioselective Alkylation of 1,4,5‐Trihydroxy‐9,10‐anthraquinone with Formaldehyde and Glyoxylic AcidAngewandte Chemie International Edition in English, 1979
- Stereoselektive Totalsynthese von AnthracyclinonenEuropean Journal of Inorganic Chemistry, 1978
- Production of nineteen anthracyclic compounds by Streptomyces galilaeus MA144-M1.The Journal of Antibiotics, 1977
- New antitumor antibiotics, aclacinomycins A and B.The Journal of Antibiotics, 1975
- Rhodomycine, VI; Antibiotica aus Actinomyceten, XLVII. ϵ‐RhodomycinonEuropean Journal of Inorganic Chemistry, 1961