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- W2017294218 abstract "An efficient synthesis of a known precursor of halicholactone (1a) and neohalicholactone (1b) has been developed using the strategically functionalized key cyclopropane intermediate 2, which in turn has been synthesized via stereoselective cyclopropanation of trans-cinnamyl alcohol in the presence of the chiral dioxaborolane ligand 4. Elaboration of the above bifunctional cyclopropane to the target molecule was achieved in a relatively short reaction sequence and in good overall yield, representing a formal synthesis of the title compounds." @default.
- W2017294218 created "2016-06-24" @default.
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- W2017294218 date "2010-06-22" @default.
- W2017294218 modified "2023-09-26" @default.
- W2017294218 title "ChemInform Abstract: Stereoselective Synthesis of a Key Precursor of Halicholactone and Neohalicholactone." @default.
- W2017294218 cites W2950983789 @default.
- W2017294218 doi "https://doi.org/10.1002/chin.199825220" @default.
- W2017294218 hasPublicationYear "2010" @default.
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