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- W2950803334 endingPage "1904" @default.
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- W2950803334 abstract "The total syntheses of the Annonaceous acetogenins squamocin A and squamocin D have been achieved. The synthesis follows a modular strategy, wherein a left-side chain, the central bis-THF core and the right-side chain are assembled together. Key reactions are additions of organomagnesium compounds to bi-THF aldehydes. At the end of the synthesis the butenolide moiety was introduced. This modular synthetic approach should be useful for the synthesis of other related natural products as well as pharmacologically interesting analogs." @default.
- W2950803334 created "2019-06-27" @default.
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- W2950803334 date "2000-05-01" @default.
- W2950803334 modified "2023-09-23" @default.
- W2950803334 title "Total Syntheses of Squamocin A and Squamocin D, Bi-tetrahydrofuran Acetogenins from Annonaceae" @default.
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- W2950803334 doi "https://doi.org/10.1002/(sici)1099-0690(200005)2000:10<1889::aid-ejoc1889>3.0.co;2-r" @default.
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