| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5288800 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Polycyclic aromatic hydrocarbons (PAH) undergo regioselective oxidative-substitution reactions with iodine(III) sulfonate reagents in dichloromethane to give the corresponding aryl sulfonate esters. The use of [hydroxy(tosyloxy)iodo]benzene in conjunction with trimethylsilyl isothiocyanate leads to thiocyanation of the PAH nucleus.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Gerald F. Koser, Sanjay Telu, Kenneth K. Laali,