Abstract
Oxidative free-radical annulation of dichloroacetophenone (7) with terminal alkenes provides modest to good yields of 4-substituted 2,2-dichloro-l-tetralones (10). The synthetic utility and reactivity of 10a is described.
- Title
- Formation of 2,2-Dichloro-1-Tetralones by Oxidative Free-Radical Annulation
- Creators
- Barry B Snider - Department of Chemistry , Brandeis UniversityLuning Han - Department of Chemistry , Brandeis University
- Publication Details
- Synthetic communications, Vol.25(15), pp.2337-2347
- Publisher
- Taylor & Francis Group
- Identifiers
- 9924012919201921
- Copyright
- © 1995 Taylor and Francis
- Academic Unit
- Department of Chemistry
- Language
- English
- Resource Type
- Journal article