Synthesis of Pyrrole Derivatives via Cycloaddition Reaction of Reissert Hydrofluoroborate Salts with α-Bromoacrylamides

Rathod, Chirag H.; Patel, Anilkumar S.

dc.contributor.author	Rathod, Chirag H.
dc.contributor.author	Patel, Anilkumar S.
dc.date.accessioned	2024-11-15T07:57:22Z
dc.date.available	2024-11-15T07:57:22Z
dc.date.issued	2021
dc.identifier.citation	Rathod, C. H., & Patel, A. S. (2021). Synthesis of Pyrrole Derivatives via Cycloaddition Reaction of Reissert Hydrofluoroborate Salts with α-Bromoacrylamides. Analytical Chemistry Letters, 11(3), 289-302.	en_US
dc.identifier.uri	http://10.9.150.37:8080/dspace//handle/atmiyauni/1534
dc.description.abstract	Abstract An investigation of α-bromoacrylamide as a dienophile for the cycloaddition reaction of Reissert hydrofluoroborate salt of quinoline/phenanthridine has been carried out. The optimized condition has been developed for the [4+2] cycloaddition reaction of Reissert hydrofluroborate salt and α-bromoacrylamide by using K2CO3 in DMF under moderate temperature to afford highly functionalized pyrrole derivatives (6a-f and 7a-f) in very good to excellent yield. The structures of newly synthesized compounds were established based on FT-IR, Mass, 1H and 13C NMR spectral techniques. Besides, the structure of compound 7a has been confirmed by 2D NMR experiments (COSY and HSQC).	en_US
dc.language.iso	en	en_US
dc.publisher	Analytical Chemistry Letters	en_US
dc.title	Synthesis of Pyrrole Derivatives via Cycloaddition Reaction of Reissert Hydrofluoroborate Salts with α-Bromoacrylamides	en_US
dc.type	Article	en_US