Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 48, Pages 16162-+Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja807026z
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Funding
- NSF [CRE-0616885]
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The first catalytic, enantioselective Meerwein-Eschenmoser Claisen rearrangement has been achieved, Palladium(II) BINAP or phosphinooxazoline catalysts were employed to generate oxindole products with 100% conversion and up to 92% ee.
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