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  Efficient synthesis of isotopically pure [O-18]-epoxides using molecular oxygen

Schöttler, M., & Boland, W. (1997). Efficient synthesis of isotopically pure [O-18]-epoxides using molecular oxygen. Synlett, (1), 91.

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Schöttler, M., Author
Boland, W.1, Author           
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1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              

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Free keywords: Kaneda-epoxidation; [O-18]-oxiranes; [O-18]-5;6- epoxycholesterol; [O-18]-epoxides of fatty acids; [O-18]- epoxyjasmonate Metal-catalysts; epoxidation; oxidation; aldehyde; epoxides; olefins; absence; acid
 Abstract: High yields of isotopically pure [O-18]-epoxides are obtained from alkenes and O-18(2) gas in the presence of isobutyraldehyde (Kaneda epoxidation). Unlike peracids, the system allows the selective epoxidation of the double bond in a keto-alkene without

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 Dates: 19971997
 Publication Status: Issued
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 Identifiers: Other: BOL037
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Title: Synlett
  Other : Synlett
Source Genre: Journal
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Publ. Info: Stuttgart : Georg Thieme Verlag
Pages: - Volume / Issue: (1) Sequence Number: - Start / End Page: 91 Identifier: ISSN: 0936-5214
CoNE: https://pure.mpg.de/cone/journals/resource/954925570856