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Enantioselective 6π Electrocyclizations: Pushing the Limits in Organocatalytic Pericyclic Reactions

机译:对映选择性6π电环化:推动有机催化周环反应的极限。

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摘要

Pericyclic reactions, which include cycloaddition reactions, sigmatropic rearrangements and electrocyclizations, represent one of the most important types of transformations in synthetic organic chemistry. Whereas a large number of methods are nowadays known for carrying out cycloaddition reactions using asymmetric catalysis and the number of reports dealing with catalytic enantioselective sigmatropic rearrangements is rapidly growing, electrocyclizations have remained as a rather unexplored field of research.
机译:周环反应包括环加成反应,σ重排和电环化,是合成有机化学中最重要的转化类型之一。如今,已知有许多使用不对称催化进行环加成反应的方法,有关催化对映选择性σ向重排的报道迅速增长,而电环化仍然是一个尚未探索的研究领域。

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