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• W2804234842 endingPage "3196" @default.
• W2804234842 startingPage "3192" @default.
• W2804234842 abstract "A new and efficient convergent approach toward the synthesis of amphidinolide F is described through the assembly of three fragments. The two trans-tetrahydrofurans were built by a diastereoselective C-glycosylation with titanium enolate of bulky N-acetyloxazolidinethiones. The side chain was inserted by a Liebeskind–Srogl cross-coupling reaction. A sulfone condensation/desulfonylation sequence, a Stille cross-coupling, and a macrolactonization were applied to connect the fragments." @default.
• W2804234842 created "2018-06-01" @default.
• W2804234842 creator A5061991312 @default.
• W2804234842 creator A5065498868 @default.
• W2804234842 creator A5071151820 @default.
• W2804234842 date "2018-05-15" @default.
• W2804234842 modified "2023-10-18" @default.
• W2804234842 title "Total Synthesis of the Marine Macrolide Amphidinolide F" @default.
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• W2804234842 doi "https://doi.org/10.1021/acs.orglett.8b01020" @default.
• W2804234842 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29762038" @default.
• W2804234842 hasPublicationYear "2018" @default.
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