Conjugate addition of nitrogen nucleophiles to an alpha,beta-unsaturated pyrrolidinone
The conjugate addition of nitrogen nucleophiles to α,β-unsaturated lactam 1b under very mild conditions occurs in good yield with high diastereoselectivity. Deprotection provides a simple access to β-aminopyrrolidinones in excellent overall yield.
Main Authors: | , , |
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Format: | Journal article |
Language: | English |
Published: |
1997
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Summary: | The conjugate addition of nitrogen nucleophiles to α,β-unsaturated lactam 1b under very mild conditions occurs in good yield with high diastereoselectivity. Deprotection provides a simple access to β-aminopyrrolidinones in excellent overall yield. |
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