Base-Catalyzed 1,6-Conjugate Addition of Nitroalkanes to p-Quinone Methides under Continuous Flow

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1749

Full metadata record

DC Field	Value	Language
dc.contributor.author	Pandey, R.	-
dc.contributor.author	Anand, R.V.	-
dc.date.accessioned	2020-11-18T05:46:42Z	-
dc.date.available	2020-11-18T05:46:42Z	-
dc.date.issued	2018	-
dc.identifier.citation	ACS Omega, 3(10), pp. 13967-13976	en_US
dc.identifier.other	10.1021/acsomega.8b01971.	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acsomega.8b01971	-
dc.identifier.uri	http://hdl.handle.net/123456789/1749	-
dc.description.abstract	A mild base-catalyzed protocol for the synthesis of substituted nitroalkane derivatives has been developed under continuous flow using a microreaction technique. This transformation basically involves the 1,6-conjugate addition of nitroalkanes to p-quinone methides, leading to the substituted nitroalkanes in good to excellent yields.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Nitroalkanes	en_US
dc.subject	p-Quinone Methides	en_US
dc.subject	Conjugate	en_US
dc.subject	Base-Catalyzed	en_US
dc.subject	Continuous Flow	en_US
dc.title	Base-Catalyzed 1,6-Conjugate Addition of Nitroalkanes to p-Quinone Methides under Continuous Flow	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

Files in This Item:

File	Description	Size	Format
Need to add pdf.odt		8.04 kB	OpenDocument Text	View/Open