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- W2079968689 abstract "Abstract A concise method leading to all stereoisomers of 1-benzyloxy-3-methyl-6-heptene-2,4-diol from (2 E ,5 E )-1,7-dibenzyloxy-2,5-heptadiene-4-ol has been developed. The first synthesis of (+)-prelactone C, a δ-lactone isolated from the concanamycin-producing Streptomyces sp. , has been achieved utilizing (2 S ,3 S ,4 R )-1-benzyloxy-3-methyl-6-heptene-2,4-diol as a chiral building block." @default.
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- W2079968689 date "2010-08-03" @default.
- W2079968689 modified "2023-09-27" @default.
- W2079968689 title "ChemInform Abstract: Enantioselective Preparation of 1-Benzyloxy-3-methyl-6-heptene-2,4- diols: Total Synthesis of (+)-Prelactone C." @default.
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- W2079968689 doi "https://doi.org/10.1002/chin.199740292" @default.
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