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- W2150376688 endingPage "2111" @default.
- W2150376688 startingPage "2105" @default.
- W2150376688 abstract "Abstract A highly efficient copper‐catalyzed enantioselective ring opening of oxabicylic alkenes with Grignard reagents has been developed by using chiral spiro phosphine ligands. Excellent trans selectivities, good yields, and high enantioselectivities are obtained for a broad range of Grignard reagents under mild reaction conditions. The catalyst system shows an extraordinary activity and the TON of the reaction reaches 9000." @default.
- W2150376688 created "2016-06-24" @default.
- W2150376688 creator A5046908754 @default.
- W2150376688 creator A5055273759 @default.
- W2150376688 creator A5075038156 @default.
- W2150376688 creator A5076699095 @default.
- W2150376688 date "2008-11-21" @default.
- W2150376688 modified "2023-10-17" @default.
- W2150376688 title "Highly Enantioselective Copper-Catalyzed Ring Opening of Oxabicyclic Alkenes with Grignard Reagents" @default.
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- W2150376688 doi "https://doi.org/10.1002/asia.200800159" @default.
- W2150376688 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18823061" @default.
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