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- W2224178857 endingPage "302" @default.
- W2224178857 startingPage "296" @default.
- W2224178857 abstract "Abstract An asymmetric Diels–Alder cycloaddition reaction of quinone imine ketals and 2,4‐dienals has been investigated via trienamine catalysis of a secondary chiral amine. A series of chiral tricyclic benzo[ de ]quinolone derivatives were efficiently constructed in moderate to good yields and with high to excellent enantioselectivity after a cascade aromatization/intramolecular hemiaminal formation sequence (up to 98% ee , >19:1 dr ). The methodology and the useful product scaffolds could be further utilized in both synthetic and medicinal fields. magnified image" @default.
- W2224178857 created "2016-06-24" @default.
- W2224178857 creator A5003877669 @default.
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- W2224178857 creator A5081529884 @default.
- W2224178857 creator A5082556661 @default.
- W2224178857 creator A5085932151 @default.
- W2224178857 date "2016-01-05" @default.
- W2224178857 modified "2023-10-15" @default.
- W2224178857 title "Asymmetric Diels–Alder and Cascade Reaction of Quinone Imine Ketals and 2,4‐Dienals: Construction of Chiral Benzo[ <i>de</i> ]quinolone Derivatives" @default.
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- W2224178857 cites W1966193020 @default.
- W2224178857 cites W1968467465 @default.
- W2224178857 cites W1969146329 @default.
- W2224178857 cites W1969568153 @default.
- W2224178857 cites W1973762773 @default.
- W2224178857 cites W1982280220 @default.
- W2224178857 cites W1999597438 @default.
- W2224178857 cites W2011973104 @default.
- W2224178857 cites W2014769801 @default.
- W2224178857 cites W2019519438 @default.
- W2224178857 cites W2025101740 @default.
- W2224178857 cites W2027812665 @default.
- W2224178857 cites W2032934117 @default.
- W2224178857 cites W2035075159 @default.
- W2224178857 cites W2038657258 @default.
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- W2224178857 cites W2042102384 @default.
- W2224178857 cites W2052055026 @default.
- W2224178857 cites W2072654506 @default.
- W2224178857 cites W2075366970 @default.
- W2224178857 cites W2076045728 @default.
- W2224178857 cites W2082644063 @default.
- W2224178857 cites W2084073443 @default.
- W2224178857 cites W2088902840 @default.
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- W2224178857 cites W2098924461 @default.
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- W2224178857 cites W2136813168 @default.
- W2224178857 cites W2137260182 @default.
- W2224178857 cites W2137584449 @default.
- W2224178857 cites W2138267367 @default.
- W2224178857 cites W2140862994 @default.
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- W2224178857 cites W2154038770 @default.
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- W2224178857 cites W2162578631 @default.
- W2224178857 cites W2167133058 @default.
- W2224178857 cites W2168271217 @default.
- W2224178857 cites W2168941067 @default.
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- W2224178857 cites W2314654991 @default.
- W2224178857 cites W2316032925 @default.
- W2224178857 cites W2316464261 @default.
- W2224178857 cites W2324033421 @default.
- W2224178857 cites W2327022512 @default.
- W2224178857 cites W2614822064 @default.
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- W2224178857 cites W2950118514 @default.
- W2224178857 cites W2950880457 @default.
- W2224178857 cites W2950930492 @default.
- W2224178857 cites W2951239749 @default.
- W2224178857 cites W2952228918 @default.
- W2224178857 cites W4229901766 @default.
- W2224178857 cites W4230596967 @default.
- W2224178857 cites W4231234416 @default.
- W2224178857 cites W4234927837 @default.
- W2224178857 cites W4235344967 @default.
- W2224178857 cites W4237995644 @default.
- W2224178857 cites W4238100063 @default.
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- W2224178857 doi "https://doi.org/10.1002/adsc.201500860" @default.
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