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- W2952392641 abstract "The (Z)-isomer of a phytotoxic nonenolide, (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9-lactone isolated from Phomopsis sp. HCCB03520 and its C-6 epimer have been synthesized through a common route starting from butyraldehyde. The synthesis involves enantioselective Maruoka allylation, Sharpless asymmetric epoxidation and intramolecular ring closing metathesis as the important steps." @default.
- W2952392641 created "2019-06-27" @default.
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- W2952392641 date "2014-01-01" @default.
- W2952392641 modified "2023-10-17" @default.
- W2952392641 title "Stereoselective total synthesis of the (Z)-isomer of a novel phytotoxic nonenolide from Phomopsis sp. HCCB03520 and its C-6 epimer" @default.
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- W2952392641 doi "https://doi.org/10.1016/j.tetlet.2013.10.114" @default.
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