Phosphine-catalyzed activation of allenoates provides efficient access to carbo- and heterocycles. However, the development of extended allenoates as synthons via this strategy remains underexplored. Herein, we report a phosphine-catalyzed remote nucleophilic addition employing α-allyl γ-benzyl allenoates as C7 synthons. This reaction proceeds through a distinctive δ to δ' addition followed by proton-promoted uncyclization, enabling efficient and highly chemoselective synthesis of cycloheptadienes from a wide range of substrates. This work establishes a versatile platform for C7 annulation, expanding the synthetic utility of phosphine catalysis beyond conventional cyclization modes.
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Xuling Pan
Yuan Liu
Hongxia Ren
Organic Letters
Nankai University
Institute of Organic Chemistry
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Pan et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69d894ce6c1944d70ce05bdb — DOI: https://doi.org/10.1021/acs.orglett.6c01074
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