156683-36-2Relevant academic research and scientific papers
Investigations on the formation of 6-hydroxyindole in the Netizescu-reaction V: Cyclization of C-(quinonylalkyl) enaminone derivatives, I
Kucklander,Lessel,Poll
, p. 143 - 155 (2007/10/02)
The labile quinonylalkylenaminones 10a-c and 11a-c are synthesized and cyclized to the products 17, 21 and 22a-c. In solution the tricyclic systems 22a-c react to spirocompounds 19a-c and 20a-c. The structure of 22a is confirmed by X-ray analysis. Semiempiric quantum chemical calculations and Pearson's concept of hard and soft acids and bases are used to explain the observed reactions.
