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- W2008043085 abstract "[structure: see text] Michael addition of Me(2)Cu(CN)Li(2) to alpha,beta-unsaturated lactone 7 derived from beta-hydroxyl ketone 5 provides lactone 8, which is converted to alcohol 11 using Oppolzer's methodology as the key step. Connection of 11 with the l-proline moiety and subsequent installation of an oxazoline ring affords 16, which is coupled with tripeptide 21; subsequent macrocyclization then furnishes 4, an oxazoline analogue of apratoxin A." @default.
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- W2008043085 date "2003-08-27" @default.
- W2008043085 modified "2023-09-26" @default.
- W2008043085 title "Synthesis of an Oxazoline Analogue of Apratoxin A" @default.
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- W2008043085 doi "https://doi.org/10.1021/ol035332y" @default.
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