Triethanolamine‐catalyzed expeditious and greener synthesis of 2‐amino‐4H‐chromenes

Patel, Anilkumar S.; Tala, Satishkumar D.; Nariya, Pankajkumar B.; Ladva, Kartik D.; Kapuriya, Naval P.

dc.contributor.author	Patel, Anilkumar S.
dc.contributor.author	Tala, Satishkumar D.
dc.contributor.author	Nariya, Pankajkumar B.
dc.contributor.author	Ladva, Kartik D.
dc.contributor.author	Kapuriya, Naval P.
dc.date.accessioned	2024-11-16T09:03:24Z
dc.date.available	2024-11-16T09:03:24Z
dc.date.issued	2019
dc.identifier.citation	Patel, A. S., Tala, S. D., Nariya, P. B., Ladva, K. D., & Kapuriya, N. P. (2019). Triethanolamine‐catalyzed expeditious and greener synthesis of 2‐amino‐4H‐chromenes. Journal of the Chinese Chemical Society, 66(3), 247-252.	en_US
dc.identifier.uri	http://10.9.150.37:8080/dspace//handle/atmiyauni/1577
dc.description.abstract	Triethanolamine (TEOA), an inexpensive and eco-friendly base, was used to efficiently catalyze the three-component condensation reaction of heterocyclic/aromatic aldehyde, (α/β)-naphthol, and malononitrile in water to give the corresponding substituted 2-amino-4H-chromene derivatives with excellent yields	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley/ Journal of the Chinese Chemical Society	en_US
dc.relation.ispartofseries	;66(3), 247-252
dc.subject	2-amino-4H-chromene	en_US
dc.subject	green synthesis	en_US
dc.subject	multicomponent reaction	en_US
dc.subject	triethanolamine (TEOA)	en_US
dc.subject	water medium	en_US
dc.title	Triethanolamine‐catalyzed expeditious and greener synthesis of 2‐amino‐4H‐chromenes	en_US
dc.type	Article	en_US