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- W4256095118 endingPage "6606" @default.
- W4256095118 startingPage "6602" @default.
- W4256095118 abstract "Abstract Phosphine‐catalyzed enantioselective annulation reactions involving ketimines are a daunting synthetic challenge owing to the intrinsic low reactivity of ketimine substrates. A highly enantioselective [3+2] cycloaddition reaction that makes use of isatin‐derived ketimines as reaction partners was developed. Notably, both simple and γ‐substituted allenoates could be utilized, and various 3,2′‐pyrrolidinyl spirooxindoles with a tetrasubstituted stereocenter were obtained in excellent yields and with nearly perfect enantioselectivity (>98 % ee in all cases)." @default.
- W4256095118 created "2022-05-12" @default.
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- W4256095118 creator A5055068824 @default.
- W4256095118 creator A5059850486 @default.
- W4256095118 creator A5066554626 @default.
- W4256095118 date "2016-04-15" @default.
- W4256095118 modified "2023-09-30" @default.
- W4256095118 title "Phosphine-mediated Highly Enantioselective Spirocyclization with Ketimines as Substrates" @default.
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