FeCl3·6H2O catalyzed diastereoselective synthesis of (L)-menthyl 4-oxo-2-arylpiperidine-3-carboxylates

dc.contributor.author	V.R., Lakshmi	en_US
dc.contributor.author	Syamala, Babu	en_US
dc.contributor.author	BHAT, RAMAKRISHNA G.	en_US
dc.date.accessioned	2019-07-01T05:32:46Z
dc.date.available	2019-07-01T05:32:46Z
dc.date.issued	2017-12	en_US
dc.identifier.citation	Tetrahedron Letters, 58(52), 4836-4840.	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3195
dc.identifier.uri	https://doi.org/10.1016/j.tetlet.2017.11.026	en_US
dc.description.abstract	An efficient diastereoselective synthesis of substituted piperidines is accomplished by using catalytic amount of FeCl3·6H2O via intramolecular aza-Michael addition of carbamate on alkylidene β-keto (L)-menthyl esters in a very short time.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier B.V.	en_US
dc.subject	Diastereoselective	en_US
dc.subject	High diastereoselectivity	en_US
dc.subject	Catalysis Cyclization Chiral	en_US
dc.subject	Auxiliary	en_US
dc.subject	17 examples with high yield	en_US
dc.subject	2017	en_US
dc.title	FeCl3·6H2O catalyzed diastereoselective synthesis of (L)-menthyl 4-oxo-2-arylpiperidine-3-carboxylates	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Tetrahedron Letters	en_US
dc.publication.originofpublisher	Foreign	en_US