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Hybrid Metal/Organo Relay Catalysis Enables Enynes To Be Latent Dienes for Asymmetric Diels–Alder Reaction

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Figshare2016-02-21 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Hybrid_Metal_Organo_Relay_Catalysis_Enables_Enynes_To_Be_Latent_Dienes_for_Asymmetric_Diels_Alder_Reaction/2530144
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The hybrid Au­(I)/Brønsted acid binary catalyst system enables enynes to serve as latent 1,3-silyloxydienes capable of participating in the first cascade hydrosiloxylation of an enynyl silanol/asymmetric Diels–Alder reaction. A variety of polycyclic compounds bearing multistereogenic centers were obtained in high yields and excellent enantioselectivities from the relay catalytic cascade reaction between (2-(but-3-en-1-ynyl)­phenyl) silanols and quinones catalyzed by the combined achiral gold complex and chiral N-triflyl phosphoramide.
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2016-02-21
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