Coupling Reaction of Alkenes with α-Bromo Carboxylic Acid Derivatives Using Nickel Boride and Borohydride Exchange Resin in Methanol
- 28 March 1998
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (8) , 2755-2757
- https://doi.org/10.1021/jo972019z
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- A New Synthesis of γ-Dialkoxy Carboxylic Acid Derivatives via Radical Coupling Reaction of α-Halo Acid Derivatives with Vinyl EthersSynlett, 1996
- Xanthate Transfer Addition of a Glycine Radical Equivalent to Alkenes. A Novel Route to .alpha.-Amino Acid DerivativesThe Journal of Organic Chemistry, 1994
- Atom transfer cyclization reactions of .alpha.-iodo esters, ketones, and malonates: examples of selective 5-exo, 6-endo, 6-exo, and 7-endo ring closuresThe Journal of Organic Chemistry, 1989
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2Synthesis, 1988
- Tri-n-butyltin Hydride as Reagent in Organic SynthesisSynthesis, 1987
- Atom transfer cyclization reactions of α-iodo carbonylsTetrahedron Letters, 1987
- Free radical annulation of cyclopentane ringTetrahedron Letters, 1986
- Mechanism of the addition of tributyltin iodoacetate to alkenesTetrahedron Letters, 1986
- Syntheses with Radicals—C-C Bond Formation via Organotin and Organomercury Compounds [New Synthetic Methods (52)]Angewandte Chemie International Edition in English, 1985
- Reactions of Atoms and Free Radicals in Solution. XII. The Addition of Bromo Esters to OlefinsJournal of the American Chemical Society, 1948