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- W2315690126 endingPage "11862" @default.
- W2315690126 startingPage "11851" @default.
- W2315690126 abstract "trans-β-Lactones are a versatile and useful class of compounds, but reliable methods for their direct synthesis are still limited. Addressing this problem, we present herein two catalysts for the regioselective carbonylation of cis-disubstituted epoxides. The two catalysts show high activities and opposing regioselectivities so that either one of the two possible β-lactone regioisomers can be obtained selectively." @default.
- W2315690126 created "2016-06-24" @default.
- W2315690126 creator A5059528800 @default.
- W2315690126 creator A5068745499 @default.
- W2315690126 date "2014-10-09" @default.
- W2315690126 modified "2023-10-10" @default.
- W2315690126 title "Carbonylation of <i>cis</i>-Disubstituted Epoxides to <i>trans</i>-β-Lactones: Catalysts Displaying Steric and Contrasteric Regioselectivity" @default.
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- W2315690126 doi "https://doi.org/10.1021/jo501899e" @default.
- W2315690126 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25299306" @default.
- W2315690126 hasPublicationYear "2014" @default.
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