Product Information
2-Methylnaphthalene-1-carbonitrile is a ferrocenyl compound that undergoes substitution reactions with bromoarenes. It is stereoselective, with the product favoring the (2E)-enantiomer. The allylation of 2-methylnaphthalene-1-carbonitrile with allyl chloride followed by hydrolysis gives the corresponding allylic alcohol in high yield. A mechanistic study has been performed on this reaction, which shows that bond cleavage occurs via a radical mechanism. This process also produces an exciplex and may be irradiated to generate singlet oxygen.
Chemical properties
Technical inquiry about: 3D-VAA94485 2-Methylnaphthalene-1-carbonitrile
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