Asymmetric Catalysis with Chiral Lewis Bases
摘要:
Catalytic, asymmetric aldol additions have come to the forefront of synthetic methodology due to both the synthetic utility of the products and the challenge of designing such a transformation. 1 There are now a number of reports concerning the addition of silyl enol ethers or silyl ketene acetals to aldehydes using chiral Lewis acids that proceed with good-to-high enantioselectivity. 2 Despite the advantages of chiral Lewis acid catalysis, an asymmetric catalytic aldol reaction with the generality and selectivity of the well known stoichiometric methods still remains to be developed. We envisioned the possibility of devising a new reaction that uses chiral Lewis base catalysis, that is, activation of the nucleophile, Scheme 1. 3 , 4
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DOI:
10.1351/pac199870081469
被引量:
年份:
1998




























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