Ingenane synthetic studies. An expedient approach to highly oxygenated ABC subunits of ingenol via reductive dialkylative annulation and .alpha.,.beta.-epoxy ketone photoisomerization
- 1 March 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 106 (5) , 1446-1454
- https://doi.org/10.1021/ja00317a043
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Synthesis of sesquiterpene antitumor lactones. 9. The hydronaphthalene route to pseudoguaianes. Total synthesis of (.+-.)-confertinJournal of the American Chemical Society, 1982
- Ingenol esters from the pro-inflammatory fraction of Euphorbia kamerunicaPhytochemistry, 1982
- Tumor-Promoting Diterpene Esters Prevent Macrophage Activation and Suppress Macrophage Tumoricidal CapacityPathobiology, 1982
- Über Inhaltsstoffe von Euphorbiaceae, 7. Mitt. 20‐Desoxyingenolmonoester und Ingenoldiester aus Euphorbia biglandulosa DesfArchiv der Pharmazie, 1982
- An approach to the total synthesis of chlorothricolide: the synthesis of the top halfThe Journal of Organic Chemistry, 1979
- TIGLIANE, DAPHNANE AND INGENANE DITERPENES, THEIR CHEMISTRY, DISTRIBUTION AND BIOLOGICAL-ACTIVITIES - REVIEW1978
- Analogs of Parasympathetic Neuroeffectors. I. Acetylselenocholine, Selenocholine, and Related Compounds1Journal of Medicinal Chemistry, 1964
- Photochemische Reaktionen. 13. Mitteilung. Zur photochemischen Umlagerung von 3‐Oxo‐4,5‐oxido‐Steroiden in 10(5→4)‐abeo‐Steroide. (Vorläufige Mitteilung)Helvetica Chimica Acta, 1962