High-Yielding Total Synthesis of Sexually Deceptive Chiloglottones and Antimicrobial Dialkylresorcinols through an Organocatalytic Reductive Coupling Reaction

dc.contributor.author Madhavachary, Rudrakshula
dc.contributor.author Ramachary, Dhevalapally B.
dc.date.accessioned 2022-03-27T09:39:27Z
dc.date.available 2022-03-27T09:39:27Z
dc.date.issued 2014-11-01
dc.description.abstract Biologically important, less-explored natural products of sexually deceptive chiloglottones, antimicrobial dialkylresorcinols, and their many analogues were synthesized in very good yields in a sequential two-pot manner by using an "organocatalytic reductive coupling reaction" as the key step. Sexually deceptive chiloglottones, antimicrobial dialkylresorcinols, and their many analogues are synthesized in very good yields in a sequential two-pot manner by using an "organocatalytic reductive coupling reaction" as the key step.
dc.identifier.citation European Journal of Organic Chemistry. v.2014(33)
dc.identifier.issn 1434193X
dc.identifier.uri 10.1002/ejoc.201403128
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/ejoc.201403128
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13164
dc.subject Natural products
dc.subject Organocatalysis
dc.subject Reductive coupling
dc.subject Resorcinols
dc.subject Total synthesis
dc.title High-Yielding Total Synthesis of Sexually Deceptive Chiloglottones and Antimicrobial Dialkylresorcinols through an Organocatalytic Reductive Coupling Reaction
dc.type Journal. Article
dspace.entity.type
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