1618099-23-2Relevant academic research and scientific papers
Novel [4 + 2]-benzannulation to access substituted benzenes and polycyclic aromatic and benzene-fused heteroaromatic compounds
Raji Reddy, Chada,Dilipkumar, Uredi,Damoder Reddy, Motatipally
supporting information, p. 3792 - 3795 (2014/08/05)
A common [4 + 2]-benzannulation of Morita-Baylis-Hillman acetates of acetylenic aldehydes with boronic acids has been developed for the synthesis of aromatic and heteroaromatic compounds through tandem allylic substitution/hydroarylative cycloisomerization process. This method provides a facile and general route to substituted benzenes, naphthalenes, other polycyclic aromatics, and various benzene-fused heteroaromatic compounds such as benzofuran, benzothiophene, indole, and carbazoles.
