Dynamic Kinetic Asymmetric Synthesis of Five Contiguous Stereogenic Centers by Sequential Organocatalytic Stetter and Michael鈭扐ldol Reaction: Enantioselective Synthesis of Fully Substituted Cyclopenta
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文摘
A synthesis of fully substituted cyclopentanes bearing a quaternary carbon center and five contiguous stereogenic centers has been achieved by sequential organocatalyzed Stetter and Michael鈭扐ldol reactions of heteroaromatic aldehydes, nitroalkenes, and 伪,尾-unsaturated aldehydes via the [1 + 2 + 2] annulation strategy with dynamic kinetic asymmetric transformation and excellent enantioselectivities (up to >99% ee).

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