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- W4232474906 endingPage "5102" @default.
- W4232474906 startingPage "5098" @default.
- W4232474906 abstract "Abstract A copper‐catalyzed asymmetric [3+2] cycloaddition of 3‐trimethylsilylpropargylic esters with either β‐naphthols or electron‐rich phenols has been realized and proceeds by a desilylation‐activated process. Under the catalysis of Cu(OAc) 2 ⋅H 2 O in combination with a structurally optimized ketimine P,N,N‐ligand, a wide range of optically active 1,2‐dihydronaphtho[2,1‐b]furans or 2,3‐dihydrobenzofurans were obtained in good yields and with high enantioselectivities (up to 96 % ee ). This represents the first desilylation‐activated catalytic asymmetric propargylic transformation." @default.
- W4232474906 created "2022-05-12" @default.
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- W4232474906 creator A5087320814 @default.
- W4232474906 date "2016-03-09" @default.
- W4232474906 modified "2023-10-18" @default.
- W4232474906 title "Desilylation‐Activated Propargylic Transformation: Enantioselective Copper‐Catalyzed [3+2] Cycloaddition of Propargylic Esters with β‐Naphthol or Phenol Derivatives" @default.
- W4232474906 cites W1965016217 @default.
- W4232474906 cites W1983625749 @default.
- W4232474906 cites W1984131070 @default.
- W4232474906 cites W1991047908 @default.
- W4232474906 cites W1991989711 @default.
- W4232474906 cites W1997890645 @default.
- W4232474906 cites W1998761932 @default.
- W4232474906 cites W2005524060 @default.
- W4232474906 cites W2006577230 @default.
- W4232474906 cites W2012671593 @default.
- W4232474906 cites W2014365787 @default.
- W4232474906 cites W2015990535 @default.
- W4232474906 cites W2019796252 @default.
- W4232474906 cites W2023625215 @default.
- W4232474906 cites W2026421941 @default.
- W4232474906 cites W2027047619 @default.
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- W4232474906 cites W2039731552 @default.
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- W4232474906 doi "https://doi.org/10.1002/ange.201510793" @default.
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