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Dinuclear Zinc-Prophenol-Catalyzed Enantioselective α-Hydroxyacetate Aldol Reaction with Activated Ester Equivalents

[Image: see text] An enantioselective α-hydroxyacetate aldol reaction that employs N-acetyl pyrroles as activated ester equivalents and generates syn 1,2-diols in good yield and diastereoselectivity is reported. This dinuclear zinc Prophenol-catalyzed transformation proceeds with high enantioselecti...

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書誌詳細
主要な著者: Trost, Barry M., Michaelis, David J., Truica, Mihai I.
フォーマット: Artigo
言語:Inglês
出版事項: 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3812954/
https://ncbi.nlm.nih.gov/pubmed/23947595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol402081p
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