Stereoselective Synthesis of α-Alkyl-β-keto Imides via Asymmetric Redox C−C Bond Formation between α-Alkyl-α-diazocarbonyl Compounds and Aldehydes
Author:
Affiliation:
1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja903500w
Reference42 articles.
1. Asymmetric acylation reactions of chiral imide enolates. The first direct approach to the construction of chiral .beta.-dicarbonyl synthons
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3. For selected examples, see:
4. Synthetic studies in the lysocellin family of polyether antibiotics. The total synthesis of ferensimycin B
5. Asymmetric Synthesis of Phorboxazole B—Part I: Synthesis of the C20-C38 and C39-C46 Subunits
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