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- W2098333228 endingPage "9317" @default.
- W2098333228 startingPage "9307" @default.
- W2098333228 abstract "The enantioselective total synthesis of the cytotoxic plecomacrolide natural product formamicin (1) is described. Key aspects of this synthesis include the efficient transacetalation reactions of MOM ethers 28 and 38 to form the seven-membered formyl acetals 29 and 39, a late-stage Suzuki cross-coupling reaction of the highly functionalized vinyl boronic acid 6 and vinyl iodide 7, a highly β-selective glycosidation reaction of β-hydroxy ketone 4 with 2,6-dideoxy-2-iodoglucopyranosyl fluoride 3, and the global desilylation of penultimate intermediate 77 mediated by in situ generated Et3N·2HF." @default.
- W2098333228 created "2016-06-24" @default.
- W2098333228 creator A5006269637 @default.
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- W2098333228 creator A5044061611 @default.
- W2098333228 creator A5045681846 @default.
- W2098333228 creator A5078844770 @default.
- W2098333228 date "2004-07-09" @default.
- W2098333228 modified "2023-10-18" @default.
- W2098333228 title "Total Synthesis of Formamicin" @default.
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