Intramolecular hydrogen abstraction. Iodosobenzene diacetate, an efficient and convenient reagent for alkoxy radical generation
- 5 March 2001
- journal article
- Published by Elsevier
- Vol. 25 (18) , 1953-1956
- https://doi.org/10.1016/s0040-4039(01)90085-1
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Intramolecular functionalization of nonactivated carbons by amidylphosphate radicals. Synthesis of 1,4-epimine compoundsThe Journal of Organic Chemistry, 1983
- Seven-membered cyclic transition state in the alkoxy-radical induced intramolecular hydrogen abstraction of 26-hydroxy-furostansTetrahedron Letters, 1983
- Aryliodine(III) dicarboxylatesChemical Society Reviews, 1981
- Nitroamine radicals as intermediates in the functionalization of non-activated carbon atomsJournal of the Chemical Society, Chemical Communications, 1980
- Functionalization at C12 of labdanolic diterpenes synthesis of α- and β-levantenolideTetrahedron Letters, 1976
- Die Hypojodit-Reaktion (Verfahren zur intramolekularen Substitution an nicht-aktivierten C-Atomen)Synthesis, 1971
- Organic Polyvalent Iodine CompoundsChemical Reviews, 1966
- Intramolecular Free‐Radical ReactionsAngewandte Chemie International Edition in English, 1964
- Reactions at Position 19 in the Steroid Nucleus. A Convenient Synthesis of 19-NorsteroidsJournal of the American Chemical Society, 1964
- Transformations of kurchi alkaloids—ITetrahedron, 1962