Iodination of alkylbenzenes with iodine and silver nitrite
β Scribed by Wing-Wah Sy; Bruce A. Lodge
- Book ID
- 104233093
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 171 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Iodination of alkylbenzenes with iodine and silver nitrite at room temperature gives iodoalkylbenzenes in good yield. Direct bromination and chlorination of aromatic compounds are well known
π SIMILAR VOLUMES
## Abstract In this study, a simple method for selective iodination of peptides and proteins is established. Using angiotensin II as the model system, we demonstrate that nitrite catalyzed the selective iodination of the peptide at the __N__βterminus in an acidic solution. The __N__βterminalβiodina
## Abslnwt: A new reagent sysrcm (silver ni~ri&odine) was developed for demonohioacekalisadon and dcdithiaacetalization madons. The reaction using his reagent t&or&d the parent carbonyl coopound in excellent yield under mild conaWns.