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- W2950335234 abstract "Abstract A variety of substituted 1-oxaspiro[4.4]non-6-ene, 1-oxaspiro[4.5]dec-6-ene, 6-oxaspiro[4.5]dec-1-ene and 1-oxaspiro[5.5]undec-7-ene systems have been prepared by utilizing Amberlyst-15-catalyzed intramolecular S N 2′ oxaspirocyclizations of secondary allylic alcohols under mild reaction conditions in quantitative yields. This oxaspirocyclization was applied to the total synthesis of theaspirane and theaspirone from β-ionone in five steps." @default.
- W2950335234 created "2019-06-27" @default.
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- W2950335234 creator A5036395533 @default.
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- W2950335234 date "2010-06-03" @default.
- W2950335234 modified "2023-09-25" @default.
- W2950335234 title "ChemInform Abstract: Amberlyst-15-Catalyzed Intramolecular SN2′ Oxaspirocyclization of Secondary Allylic Alcohols. Application to the Total Synthesis of Spirocyclic Ethers Theaspirane and Theaspirone." @default.
- W2950335234 cites W1974731998 @default.
- W2950335234 doi "https://doi.org/10.1002/chin.200032038" @default.
- W2950335234 hasPublicationYear "2010" @default.
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