Highly enantioselective [4+2] annulation via organocatalytic Mannich-reductive cyclization: one-pot synthesis of functionalized piperidines

dc.contributor.authorKumar, Indresh
dc.date.accessioned2021-10-27T04:27:59Z
dc.date.available2021-10-27T04:27:59Z
dc.date.issued2013
dc.description.abstractA new method for one-pot synthesis of 2,3-substituted piperidine from N-PMP aldimine and aqueous glutaraldehyde via formal [4+2] cycloaddition is reported. This reaction involves organocatalytic direct Mannich reaction–reductive cyclization with high yields (up to 90%) and excellent enantioselectivities (up to >99%). The practicability of this method is also shown at a gram scale as well as through the synthesis of functionalized (−)-anabasineen_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2013/cc/c3cc42431f
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3175
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectEnantioselective [4+2]en_US
dc.subjectOrganocatalyticen_US
dc.titleHighly enantioselective [4+2] annulation via organocatalytic Mannich-reductive cyclization: one-pot synthesis of functionalized piperidinesen_US
dc.typeArticleen_US

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