Studies on the syntheses of heterocyclic compounds. Part DXCVII. A synthesis of dienone analogs by electrolytic oxidation
Authors:
- 1 April 1975
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 12 (2) , 305-307
Abstract
Electrolytic coupling reaction of laudanosine (1) gave the O‐methylflavinantine (II). N‐Ethoxycarbonylated dihydrostilbene (IVa) gave a rearranged dienone (Va) and N‐trifluoro‐acetylated dihydrostilbene (IVb) contrastively gave an unrearranged dienone (Vb).Keywords
This publication has 8 references indexed in Scilit:
- Anodic cyclization-rearrangement of methoxybibenzyls to dihydrophenanthronesJournal of the American Chemical Society, 1974
- A new synthesis of the alkaloid (±)-colchicineJournal of the Chemical Society, Chemical Communications, 1974
- Electrooxidative cyclization of 1-benzyltetrahydroisoquinolines. Novel nonphenol coupling reactionJournal of the American Chemical Society, 1973
- Total synthesis of the morphinandienone alkaloids, (±)-amurine, (±)-flavinantine, and (±)-pallidine by anodic oxidationTetrahedron Letters, 1973
- Electrooxidative cyclization of laudanosine. Novel nonphenolic coupling reactionJournal of the American Chemical Society, 1971
- Structure of Erybidine, a New Alkaloid from Erythrina xbidwilli LINDLChemical and Pharmaceutical Bulletin, 1971
- Studies on the Syntheses of Heterocyclic Compounds. CCXII. : By-product in the Preparation of Homoveratrylamine by Catalytic Hydrogenation of 3, 4-Dimethoxybenzyl Cyanide and its Derivation to 2-Phenethylisoquinoline DerivativesYAKUGAKU ZASSHI, 1968
- One-step synthesis of morphinandienone-type compoundsChemical Communications (London), 1968