Asymmetric synthesis of the β-lactam framework via a three-component coupling reaction

Abstract
The reaction of the chiral lithium amide 4 with the dienoate 5a provides regio- and stereo-selectively the β-amino ester 8 in essentially quantitative yield with >99% diastereoisomeric excess, which can be converted upon sequential treatment with LiNPri 2–B(OMe)3–MeCHO to the key intermediate 6 for the β-lactam 7 having the correct absolute configuration.

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