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• W1995659816 abstract "A flexible non-amino acid-based formal asymmetric synthesis of naturally occurring antimicrobial (2R,3S)-2-aminotetradeca-5,7-dien-3-ol is reported. The method features a flexible and highly regioselective Grignard addition to (S)-malimide followed by a trans-diastereoselective reductive deoxygenation. The scope and limitations of the highly regio and diastereoselective reductive alkylation of malimides were defined. A remarkable protecting group effect on the regio and diastereoselective reductive alkylation of malimides was observed." @default.
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• W1995659816 date "2003-07-01" @default.
• W1995659816 modified "2023-10-03" @default.
• W1995659816 title "A flexible non-amino acid-based formal asymmetric synthesis of naturally occurring (2R,3S)-2-aminotetradeca-5,7-dien-3-ol: observation of a remarkable protecting group effect" @default.
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• W1995659816 doi "https://doi.org/10.1016/s0957-4166(03)00442-7" @default.
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