Synthesis of Highly Functionalized Pyrrolidine Derivatives from Easily Accessible Diethyl (E)-4-Oxohex-2-enedioate

dc.contributor.author	Kumar Thota, Ganesh
dc.contributor.author	Tamilarasan, Duraiyarasu
dc.contributor.author	Balamurugan, Rengarajan
dc.date.accessioned	2022-03-27T08:39:04Z
dc.date.available	2022-03-27T08:39:04Z
dc.date.issued	2017-11-24
dc.description.abstract	The diastereoselective synthesis of highly substituted pyrrolidines has been accomplished using a six-carbon building block bearing carbon atoms with different reactivities. In this reaction, the building block acts a 1,3-dipole and undergoes cyclization with imines formed in situ to give pyrrolidine derivatives.
dc.identifier.citation	European Journal of Organic Chemistry. v.2017(43)
dc.identifier.issn	1434193X
dc.identifier.uri	10.1002/ejoc.201700997
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/ejoc.201700997
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/11365
dc.subject	1,3-Dipoles
dc.subject	Amines
dc.subject	Cycloaddition
dc.subject	Lactams
dc.subject	Nitrogen heterocycles
dc.title	Synthesis of Highly Functionalized Pyrrolidine Derivatives from Easily Accessible Diethyl (E)-4-Oxohex-2-enedioate
dc.type	Journal. Article
dspace.entity.type

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