244-92-8Relevant academic research and scientific papers
One-pot synthesis of phthalazines and pyridazino-aromatics: A novel strategy for substituted naphthalenes
Kessler, Simon N.,Wegner, Hermann A.
supporting information; experimental part, p. 3268 - 3271 (2012/08/28)
A new one-pot strategy for the synthesis of phthalazines and pyridazino-aromatics starting from aromatic aldehydes has been developed. A variety of substituents ranging from electron withdrawing to donating is tolerated furnishing the desired 1,2-diazine in good to excellent yields. The products have been applied to the bidentate Lewis acid catalyzed inverse electron-demand Diels-Alder (IEDDA) reaction opening a novel two-step entry into substituted naphthalenes, such as Naproxen.
Synthesis and Diels-Alder reactions of the benzo[4,5]thieno [2,3-c]pyrrole ring system
Sha, Chin-Kang,Hsu, Hsi-Yen,Cheng, Su-Ya,Kuo, Yuan-Liang
, p. 1477 - 1481 (2007/10/03)
The first synthesis of the parent compound of the benzo[4,5]thieno[2,3-c]pyrrole ring system and its derivatives, as well as their Diels-Alder reactions with DMAD and N-phenylmaleimide are reported. A new synthesis of the benzo[4,5]thieno[2,3-d]pyridazine ring system is also described.
