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- W2952287875 abstract "Combinatorial coordination chemistry strategy combined with high-throughput screening techniques has been successfully applied to engineering practical enantioselective catalysts for asymmetric hetero-Diels−Alder reaction. The reaction of Danishefsky's diene with a variety of aldehydes can be carried out with 0.1−0.005 mol % of H4-BINOL/Ti/H4-BINOL or H4-BINOL/Ti/H8-BINOL catalysts at room temperature under solvent- and MS-free conditions to afford dihydropyrone derivatives with up to quantitative yield and 99.8% ee." @default.
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- W2952287875 date "2010-05-21" @default.
- W2952287875 modified "2023-09-24" @default.
- W2952287875 title "ChemInform Abstract: Discovery of Exceptionally Efficient Catalysts for Solvent-Free Enantioselective Hetero-Diels-Alder Reaction." @default.
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- W2952287875 doi "https://doi.org/10.1002/chin.200224034" @default.
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