Chiral pool approach to the total synthesis of phomonol

dc.contributor.author Dada, Ravikrishna
dc.contributor.author Yaragorla, Srinivasarao
dc.date.accessioned 2022-03-27T08:48:56Z
dc.date.available 2022-03-27T08:48:56Z
dc.date.issued 2022-01-01
dc.description.abstract We report a stereoselective total synthesis of a natural product, phomonol, from readily available D-aspartic acid. The key steps include Wittig olefination, Sharpless asymmetric dihydroxylation, Grignard addition, diastereoselective reductive etherification and Wacker oxidation.
dc.identifier.citation Synthetic Communications
dc.identifier.issn 00397911
dc.identifier.uri 10.1080/00397911.2022.2031223
dc.identifier.uri https://www.tandfonline.com/doi/full/10.1080/00397911.2022.2031223
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11853
dc.subject hiral pool
dc.subject natural products
dc.subject reductive etherification
dc.subject sharpless asymmetric dihydroxylation
dc.subject Total synthesis
dc.title Chiral pool approach to the total synthesis of phomonol
dc.type Journal. Article
dspace.entity.type
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