347335-60-8Relevant articles and documents
The Vilsmeier cyclization of 2′-azido and 2′-aminochalcones - A mild one pot synthesis of 2-aryl-4-chloroquinoline and its N-formyl-1,2-dihydro derivatives
Akila, Shanmugam,Selvi, Srinivasan,Balasubramanian, Krishna
, p. 3465 - 3469 (2001)
The Vilsmeier cyclization of 2′-aminochalcones provides a mild one pot synthesis of 2-aryl-4-chloro-N-formyl-1,2-dihydroquinolines. The scope of the reaction has been extended for the synthesis of quinolines themselves, by replacing 2′-aminochalcones with 2′-azidochalcones as the starting material. The yields are reasonably good and a plausible mechanism for the formation of the products in each case has been discussed.
Intramolecular cyclization of 2′-aminochalcones by halomethyleniminium salts derived from btc/dmf
Su, Weike,Li, Zhen-Hua,Zheng, Cun,Chen, Ren-Er
experimental part, p. 156 - 161 (2009/12/24)
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