371964-02-2Relevant academic research and scientific papers
Transition-metal-promoted 6-endo-dig cyclization of aromatic enynes: Rapid synthesis of functionalized naphthalenes
Dankwardt, John W.
, p. 5809 - 5812 (2001)
Transition-metal-mediated cyclization of aromatic enynes provides high yields of sustituted naphtalene compounds. The reduction can tolerate a wide range of substituents on both the olefin and the alkyne. The most useful catalysts were found to be [Rh(CO)
