Efficient α-Halogenation of Carbonyl Compounds by N-Bromosuccinimide and N-Chlorosuccinimde
- 20 April 2003
- journal article
- Published by Korean Chemical Society in Bulletin of the Korean Chemical Society
- Vol. 24 (4) , 407-408
- https://doi.org/10.5012/bkcs.2003.24.4.407
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- A facile protocol for the convenient preparation of amino-substituted α-bromo- and α,α-dibromo arylmethylketonesTetrahedron Letters, 1998
- Ultrasound Promoted Bromination of Activated Arenes withN-BromosuccinimideSynthetic Communications, 1995
- Synthetic methods and reactions. 181. Iodination of deactivated aromatics with N-iodosuccinimide in trifluoromethanesulfonic acid (NIS-CF3SO3H) via in situ generated superelectrophilic iodine(I) trifluoromethanesulfonateThe Journal of Organic Chemistry, 1993
- Synthesis of Bromoacetyl Derivatives by Use of Tetrabutylammonium TribromideBulletin of the Chemical Society of Japan, 1987
- Halogenation of Aromatic Compounds by N-Bromo- and N-Chlorosuccinimide under Ionic ConditionsThe Journal of Organic Chemistry, 1965
- Selective Bromination with Copper(II) Bromide1The Journal of Organic Chemistry, 1964
- The Chlorination of Active Hydrogen Compounds with Sulfuryl Chloride. I. KetonesThe Journal of Organic Chemistry, 1964
- Halogenation with Copper(II). I. Saturated Ketones and PhenolThe Journal of Organic Chemistry, 1963