CuI-catalyzed domino reactions for the synthesis of benzoxazine-fused isoquinolines under microwave irradiation was written by Zhao, Yun-Hui;Li, Yubo;Guo, Tao;Tang, Zilong;Deng, Keqin;Zhao, Gang. And the article was included in Synthetic Communications in 2016.Related Products of 1186603-47-3 The following contents are mentioned in the article:
A small library of benzoxazine-fused isoquinolines, e.g., I, were synthesized under microwave irradiation via CuI-catalyzed domino reactions of o-alkynyl aldehydes and amines having embedded nucleophiles. This strategy offered a operationally simple, environmentally acceptable route to synthesize the benzoxazine-fused isoquinolines in moderate to good yields. All new compounds were characterized by 1H NMR, 13C NMR, IR, and high-resolution mass spectrometry techniques. This study involved multiple reactions and reactants, such as 5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3Related Products of 1186603-47-3).
5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Related Products of 1186603-47-3
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics