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- W2013204773 abstract "Abstract Based on a retrosynthetic analysis, a concept for the synthesis of all stereoisomers of the C(1)‐to‐C(6) segment of phomenoic acid has been developed. Both enantiomers of the chiral synthon 9 were prepared starting from rac ‐epoxy‐diester 10 . They were converted to both enantiomers of the epoxyalcohol, 16 and 21 , respectively, using Sharpless epoxydation. They served as building blocks for the synthesis of the tetrol derivatives 20 and 22 , respectively. All four stereoisomers were obtained in optically pure form. They contain the correct assembly of protected functional groups, allowing selective deprotection in view of further transformations." @default.
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- W2013204773 date "1994-05-11" @default.
- W2013204773 modified "2023-10-01" @default.
- W2013204773 title "Studies Directed toward the Synthesis of Phomenoic Acid. Part 1. Enantioselective synthesis of the C(1)‐to‐C(6) segment" @default.
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- W2013204773 doi "https://doi.org/10.1002/hlca.19940770323" @default.
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