Gold-Catalyzed Highly Regioselective Coupling Reaction between Alkynes and Aldehydes for the Synthesis of Conjugated Enones

dc.contributor.author	Gudla, Vanajakshi
dc.contributor.author	Swamy, Kolukuluri Chaguru
dc.contributor.author	Battula, Venkateswara Rao
dc.date.accessioned	2022-03-27T09:47:52Z
dc.date.available	2022-03-27T09:47:52Z
dc.date.issued	2018-05-08
dc.description.abstract	An efficient AuCl3/AgSbF6-catalysed enone synthesis from coupling of alkynes and aldehydes has been presented. The present reaction is very effective, simple and mild and has wide range of substrate scope. Both aryl (electron rich and electron deficient) and aliphatic aldehydes and terminal and internal arylalkynes participated smoothly in the reaction and provided exclusively trans product. This simple reaction can be coupled with other gold catalysed transformations which involve enones as substrates for further development.
dc.identifier.citation	ChemistrySelect. v.3(17)
dc.identifier.uri	10.1002/slct.201800371
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/slct.201800371
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13315
dc.subject	aldehydes
dc.subject	alkynes
dc.subject	enones
dc.subject	gold catalysis
dc.subject	metathesis
dc.title	Gold-Catalyzed Highly Regioselective Coupling Reaction between Alkynes and Aldehydes for the Synthesis of Conjugated Enones
dc.type	Journal. Article
dspace.entity.type

Now showing 1 - 1 of 1