Organocatalytic enantiospecific total synthesis of butenolides

dc.contributor.author	Madhavachary, Rudrakshula
dc.contributor.author	Mallik, Rosy
dc.contributor.author	Ramachary, Dhevalapally B.
dc.date.accessioned	2022-03-27T09:36:36Z
dc.date.available	2022-03-27T09:36:36Z
dc.date.issued	2021-07-02
dc.description.abstract	Biologically important, chiral natural products of butenolides, (-)-blastmycinolactol, (+)-blastmycinone, (-)-NFX-2, (+)-antimycinone, lipid metabolites, (+)-ancepsenolide, (+)-homoancepsenolide, mosquito larvicidal butenolide and their analogues were synthesized in very good yields in a sequential one-pot manner by using an organocatalytic reductive coupling and palladium-mediated reductive deoxygenation or organocatalytic reductive coupling and silica-mediated reductive deamination as the key steps.
dc.identifier.citation	Molecules. v.26(14)
dc.identifier.uri	10.3390/molecules26144320
dc.identifier.uri	https://www.mdpi.com/1420-3049/26/14/4320
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13110
dc.subject	Butenolides
dc.subject	Deoxygenation
dc.subject	Organocatalysis
dc.subject	Proline
dc.subject	Reductive coupling
dc.subject	Total synthesis
dc.title	Organocatalytic enantiospecific total synthesis of butenolides
dc.type	Journal. Article
dspace.entity.type

Now showing 1 - 1 of 1