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Complete Characterization of a Chiral Lewis Acid-Product Complex for the Enantioselective Diels-Alder Reaction between Methacrolein and Cyclopentadiene: Mechanistic Considerations
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文摘
The Diels-Alder reaction between methacrolein andcyclopentadiene catalyzed by [(5-C5Me5)Ir{(R)-Prophos}(methacrolein)][SbF6]2 is inhibited by the products, this featureallowing, for the first time, the spectroscopic and crystallographic characterization of the major Lewis acid-productintermediate involving an enal as a dienophile.

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