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• W2022834076 abstract "An enantioselective route to the oxatetracyclic core of (−)-platensimycin (1) has been investigated by using an intramolecular Diels−Alder reaction as the key step. The thermal reaction of E/Z mixture (1:1) provided oxatetracyclic core 2 from the E-diene and the Z-diene was recovered unchanged. The Diels−Alder substrate was conveniently assembled in optically active form with use of (S)-carvone as the starting material." @default.
• W2022834076 created "2016-06-24" @default.
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• W2022834076 date "2007-09-01" @default.
• W2022834076 modified "2023-09-26" @default.
• W2022834076 title "Enantioselective Synthesis of (−)-Platensimycin Oxatetracyclic Core by Using an Intramolecular Diels−Alder Reaction" @default.
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• W2022834076 doi "https://doi.org/10.1021/ol701783z" @default.
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