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- W3084284706 endingPage "5001" @default.
- W3084284706 startingPage "4996" @default.
- W3084284706 abstract "A palladium-catalyzed domino spiro-cyclization of carbamoyl chlorides with alkynes and benzynes, involving intramolecular C−H activation to afford valuable oxindole scaffolds bearing spiro quaternary stereocenters, has been developed. This one-step synthesis of spirooxindole is both step- and atom-economic, proceeding with high regioselectivity in moderate to excellent yields." @default.
- W3084284706 created "2020-09-14" @default.
- W3084284706 creator A5001618715 @default.
- W3084284706 creator A5010266933 @default.
- W3084284706 creator A5029322489 @default.
- W3084284706 creator A5031524684 @default.
- W3084284706 creator A5051578642 @default.
- W3084284706 date "2020-09-24" @default.
- W3084284706 modified "2023-10-17" @default.
- W3084284706 title "Palladium‐Catalyzed Regioselective Domino Spirocyclization of Carbamoyl Chlorides with Alkynes and Benzynes" @default.
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