Side chain bromination of mono and dimethyl heteroaromatic and aromatic compounds by solid phase N-bromosuccinimide reaction without radical initiator under …
A series of side chain mono and dibromo derivatives of mono and dimethyl heteroaromatic and aromatic compounds (1–17) were synthesized by one step solid phase N- bromosuccinimide (NBS) reaction without radical initiator by microwave irradiation. The benzylic mono and dibromo products were exclusively preferred except in the case of 6- methylpyridine amides (8 and 9) where nuclear and also side chain bromination resulted. ...
[Maidwell, Nicola L.; Reza Rezai; Roeschlaub, Carl A.; Sammes, Peter G. Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 10 p. 1541 - 1546]
[Maidwell, Nicola L.; Reza Rezai; Roeschlaub, Carl A.; Sammes, Peter G. Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 10 p. 1541 - 1546]