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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3175
Title: Highly enantioselective [4+2] annulation via organocatalytic Mannich-reductive cyclization: one-pot synthesis of functionalized piperidines
Authors: Kumar, Indresh
Keywords: Chemistry
Enantioselective [4+2]
Organocatalytic
Issue Date: 2013
Publisher: RSC
Abstract: A 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 (−)-anabasine
URI: https://pubs.rsc.org/en/content/articlelanding/2013/cc/c3cc42431f
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3175
Appears in Collections:Department of Chemistry

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