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NaIO4-mediated C–H activation of alkylbenzenes and alkanes with LiBr
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Aug2005, Vol. 46 Issue 33, p5589-5592. 4p. - Publication Year :
- 2005
-
Abstract
- Abstract: NaIO4 oxidizes lithium bromide efficiently under acidic conditions to functionalize alkylbenzenes and alkanes and produce the corresponding bromo and acetoxy derivatives in excellent yields. The protocol also demonstrates the direct conversion of cyclohexane into trans-1,2-dibromocyclohexane in moderate yield. [Copyright &y& Elsevier]
- Subjects :
- *ALIPHATIC compounds
*ALKANES
*LITHIUM
*ALKALI metals
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 46
- Issue :
- 33
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18135247
- Full Text :
- https://doi.org/10.1016/j.tetlet.2005.06.033