A stereoselective synthesis of the reported structure of polyporolide
DSpace at IIT Bombay
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Title |
A stereoselective synthesis of the reported structure of polyporolide
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Creator |
PATIL, PH
FERNANDES, RA |
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Subject |
RING-CLOSING METATHESIS
HAGENS GLAND LACTONES ASYMMETRIC EPOXIDATION ALLYLIC ALCOHOLS EPOXY ALCOHOLS LIGAND CLASS DIHYDROXYLATION ACID CATALYSTS ANALOGS |
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Description |
Polyporolide, isolated from a basidiomycete, was assigned a 4-hydroxy-5-(1-hydroxyhexyl)-dihydrofuran-2- one structure with anti-placement of the three contiguous stereocenters. A stereoselective total synthesis of the reported structure of the natural product involving two different routes is presented. A comparison of the spectral data of the synthesized molecule indicates the need for structure revision of natural polyporolide.
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Publisher |
ROYAL SOC CHEMISTRY
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Date |
2016-01-15T07:22:41Z
2016-01-15T07:22:41Z 2015 |
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Type |
Article
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Identifier |
RSC ADVANCES, 5(61)49189-49194
2046-2069 http://dx.doi.org/10.1039/c5ra07930f http://dspace.library.iitb.ac.in/jspui/handle/100/18039 |
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Language |
en
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