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Efficient access to multiple functionalized allenes via a three component 1,4-alkylcyanation of enynes with cyclic alcohol derivatives in the presence of trimethylsilyl cyanide (TMSCN) under copper/photoredox dual catalysis has been developed. Both easily transformable aldehyde and cyano groups were introduced to tetra-substituted allenes through light-induced C–C bond cleavage of cyclic butanol and pentanol derivatives. The reactions proceeded smoothly under mild conditions with broad functional groups tolerance.
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Pu et al. (Thu,) studied this question.
www.synapsesocial.com/papers/68e780b7b6db6435876f36ba — DOI: https://doi.org/10.1021/acs.orglett.3c04360
Yue Pu
Shumin Ding
Hai‐Xia Zhao
Organic Letters
Anhui Normal University
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