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[摘要]:A highly efficient asymmetric Michael addition of 1-acetylindolin-3-ones to alpha,beta-unsaturated aldehydes is developed to afford 2-substituted indolin-3-one derivatives in high yields (up to 94%) with good stereoselectivities (up to 11:1 dr and 96% ee). The Michael adducts can be transformed into substituted cyclopentyl[b]indoline compounds conveniently without racemization. |
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