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- W2065646412 endingPage "4372" @default.
- W2065646412 startingPage "4372" @default.
- W2065646412 abstract "A diastereo- and enantio-selective domino Michael-cyclization–tautomerization reaction of isatylidene malononitriles with α,α-dicyanoalkenes catalyzed by a cinchona alkaloid-derived bifunctional thiourea catalyst has been developed. A series of multi-functionalized spiro oxindole diene derivatives have been obtained in good to excellent yields (up to 97%) with good to excellent enantioselectivities (up to 96%) as well as good diastereoselectivities (up to 7.9 : 1). In addition, an anomalous temperature effect on the enantioselectivity has also been studied for this transformation." @default.
- W2065646412 created "2016-06-24" @default.
- W2065646412 creator A5036990231 @default.
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- W2065646412 creator A5077886876 @default.
- W2065646412 creator A5089547589 @default.
- W2065646412 creator A5089680532 @default.
- W2065646412 date "2014-01-01" @default.
- W2065646412 modified "2023-09-27" @default.
- W2065646412 title "Organocatalytic enantioselective construction of multi-functionalized spiro oxindole dienes" @default.
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