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- W2397806695 abstract "The allylic ester (I), prepared by an asymmetric aldol synthesis, is subjected to the silyl keteneacetal modification of the Claisen rearrangement, yielding the acids (II) or (III)." @default.
- W2397806695 created "2016-06-24" @default.
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- W2397806695 date "1987-04-28" @default.
- W2397806695 modified "2023-09-26" @default.
- W2397806695 title "ChemInform Abstract: Acyclic Stereoselection. Part 37. Total Synthesis of a Slightly Unnatural Product. Confirmation of the Stereostructure of the Archaebacterial C40 Diol by Synthesis of a Stereoisomer." @default.
- W2397806695 cites W1986763577 @default.
- W2397806695 doi "https://doi.org/10.1002/chin.198717320" @default.
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