Ligand- and Base-Free Access to Diverse Biaryls by the Reductive Coupling of Diaryliodonium Salts

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3027

Full metadata record

DC Field	Value	Language
dc.contributor.author	Kumar, Dalip	-
dc.date.accessioned	2021-10-27T04:19:27Z	-
dc.date.available	2021-10-27T04:19:27Z	-
dc.date.issued	2016-04	-
dc.identifier.uri	https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201600242	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3027	-
dc.description.abstract	The ligand- and base-free, Pd-catalyzed synthesis of useful symmetrical and unsymmetrical biaryls in high yields from stable diaryliodonium salts is developed. The reaction is catalyzed by a recyclable Pd/polyethylene glycol-400 (PEG-400) system and proceeds under mild reaction conditions to produce biaryls that can be utilized to synthesize an array of natural and druglike compounds.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Diaryliodonium Salts	en_US
dc.title	Ligand- and Base-Free Access to Diverse Biaryls by the Reductive Coupling of Diaryliodonium Salts	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

Files in This Item:

There are no files associated with this item.