A total synthesis of (±) steganacin via the modified Ullmann reaction
- 1 January 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (31) , 2767-2770
- https://doi.org/10.1016/s0040-4039(01)94857-9
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthetic studies on lignan lactones: aryl dithiane route to (.+-.)-podorhizol and (.+-.)-isopodophyllotoxone and approaches to the stegane skeletonThe Journal of Organic Chemistry, 1978
- The chemospecific, homogeneous, ambient temperature Ullmann coupling of o-haloaryliminesJournal of the American Chemical Society, 1976
- IsosteganacinJournal of the American Chemical Society, 1976
- Total synthesis of (+-)-steganacinJournal of the American Chemical Society, 1976
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compoundsTetrahedron Letters, 1975
- Tumor inhibitors. LXXXX. Steganacin and steganangin, novel antileukemic lignan lactones from Steganotaenia araliaceaJournal of the American Chemical Society, 1973