Organocatalytic enantiospecific total synthesis of butenolides
Organocatalytic enantiospecific total synthesis of butenolides
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Date
2021-07-02
Authors
Madhavachary, Rudrakshula
Mallik, Rosy
Ramachary, Dhevalapally B.
Journal Title
Journal ISSN
Volume Title
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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.
Description
Keywords
Butenolides,
Deoxygenation,
Organocatalysis,
Proline,
Reductive coupling,
Total synthesis
Citation
Molecules. v.26(14)