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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3178
Title: An organocatalytic direct Mannich–cyclization cascade as [3+2] annulation: asymmetric synthesis of 2,3-substituted pyrrolidines
Authors: Kumar, Indresh
Keywords: Chemistry
Organocatalytic
Mannich–cyclization
Pyrrolidines
Issue Date: 2012
Publisher: RSC
Abstract: A new method for asymmetric synthesis of 2,3-substituted pyrrolidines from N-PMP aldimines and succinaldehyde via formal [3+2] cycloaddition is reported. This reaction involves proline catalyzed direct Mannich reaction and acid catalyzed reductive cyclization with high yields (up to 78%) and excellent enantioselectivities (up to >99%).
URI: https://pubs.rsc.org/en/content/articlelanding/2012/cc/c2cc33103a
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3178
Appears in Collections:Department of Chemistry

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