Amino Acids Chirons: A Tool for Asymmetric synthesis of Heterocycles

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dc.contributor.author Singh, Priyanka
dc.contributor.author Samanta, Krishnananda
dc.contributor.author Das, S K
dc.contributor.author Panda, Gautam
dc.date.accessioned 2014-09-23T05:41:50Z
dc.date.available 2014-09-23T05:41:50Z
dc.date.issued 2014
dc.identifier.citation Organic Biomolecular Chemistry, 2014,12, 6297-6339 en
dc.identifier.uri http://hdl.handle.net/123456789/1412
dc.description.abstract Amino acids as chiral pool have been extensively used by synthetic organic and medicinal chemists for access to heterocycles (monocycles, bicycles or polycycles either bridged or fused) owing to their easy availability in enantiomerically enriched form and having synthetically transformable diverse functional groups. This review describes diverse asymmetric heterocycles with various membered rings (n=3-9) followed by benzo or heteroannulated ones for the period from 1996 to Dec, 2013. It details on those solution phase synthetic methodologies in which the naturally occurring α-amino acid is incorporated, totally or partially, in the final product. en
dc.format.extent 2393230 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI communication No. 8716 en
dc.subject Amino acids en
dc.subject Asymmetric synthesis en
dc.subject Heterocycles en
dc.title Amino Acids Chirons: A Tool for Asymmetric synthesis of Heterocycles en
dc.type Article en


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