Radical Addition of 2-Iodoalkanamide or 2-Iodoalkanoic Acid to Alkenes with a Water-Soluble Radical Initiator in Aqueous Media: Facile Synthesis of γ -Lactones
- 1 October 2001
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 74 (10) , 1963-1970
- https://doi.org/10.1246/bcsj.74.1963
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Powerful Solvent Effect of Water in Radical Reaction: Triethylborane-Induced Atom-Transfer Radical Cyclization in WaterJournal of the American Chemical Society, 2000
- Free-Radical Reaction of Imine Derivatives in WaterThe Journal of Organic Chemistry, 2000
- Efficient Large-Scale Radical Deoxygenation in Alcoholic Solvents Using Sodium Hypophosphite and a Phase-Transfer Agent: Application to ErythromycinsThe Journal of Organic Chemistry, 2000
- Radical addition of 2-iodoalkanamide or 2-iodoalkanoic acid to alkenols using a water-soluble radical initiator in water. A facile synthesis of γ-lactonesTetrahedron Letters, 1999
- Triethylborane-Mediated Atom Transfer Radical Cyclization Reaction in WaterThe Journal of Organic Chemistry, 1998
- Novel Water-Soluble Organosilane Compounds as a Radical Reducing Agent in Aqueous MediaBulletin of the Chemical Society of Japan, 1997
- Organometallic reactions in aqueous media with indiumTetrahedron Letters, 1991
- Additional flexibility solves the leaving group problem in cyclodextrin acylationTetrahedron Letters, 1990
- Conjugate additions to α,β-unsaturated carbonyl compounds in aqueous mediaTetrahedron Letters, 1986
- Hydrophobic acceleration of Diels-Alder reactionsJournal of the American Chemical Society, 1980