Synthesis of Functionalized Cyclobutenes and Spirocycles <i>via</i> Asymmetric P(III)/P(V) Redox Catalysis

نویسندگان

چکیده

An enantioselective phosphine-catalyzed transformation has been developed for the synthesis of chiral cyclobutene triesters and fluorinated spirocyclic compounds. The strategy involved a P(III)/P(V) redox cycling process, via in situ reduction phosphine oxide with phenylsilane. This catalytic methodology enabled functionalized cyclobutenes (24 examples, up to 94% ee). On occasion extension this study α-ketoester indenone substrates, surprising reactivity discovered spiro-indenone products.

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ژورنال

عنوان ژورنال: Advanced Synthesis & Catalysis

سال: 2021

ISSN: ['1615-4169', '1615-4150']

DOI: https://doi.org/10.1002/adsc.202100664