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• W1984831462 abstract "A simple and straightforward stereoselective synthesis of α,β-unsaturated δ-lactone, (−)-cleistenolide has been accomplished in 10 steps in an overall yield of 19%, starting from inexpensive and commercially available starting materials, respectively. This linear synthesis utilizes Sharpless asymmetric dihydroxylation, sulfur ylide mediated epoxide opening followed by ring-closing metathesis (RCM) for the formation of six-membered lactone ring as the key step sequence." @default.
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• W1984831462 date "2012-04-01" @default.
• W1984831462 modified "2023-09-23" @default.
• W1984831462 title "A simple and efficient stereoselective synthesis of (−)-cleistenolide" @default.
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• W1984831462 doi "https://doi.org/10.1016/j.tetlet.2012.01.123" @default.
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