Synthesis demonstrates a convergent strategy to generate (17S,18S,36S)-tonkinelin and its diastereomer, suggesting significant potential in organic synthesis.
We report the stereoselective synthesis of (17S,18S,36S)-tonkinelin and its diastereomer (17R,18R,36S)-tonkinelin via a convergent strategy involving the stepwise construction of two key fragments - a chiral ester-derived phosphonium salt and...
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Fernandes et al. (2025) studied this question.
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