Conclusions
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1.
Benzoyl and trichloroacetyl isocyanates react with electrophilic reagents with greater difficulty than with nucleophilic reagents.
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2.
Benzoyl isocyanate reacts with ethylpropionate, propargylmethyl ether, and cis-dichloroethylene according to a scheme of 1,2-cycloaddition.
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3.
Trichloroacetyl isocyanate interacts with propargylmethyl ether according to the type of 1,2-cy-cloaddition and according to the type of substitutional addition.
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4.
A dimer of benzoyl isocyanate was produced, and its structure was established.
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Literature cited
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1570–1574, July, 1970.
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Arbuzov, B.A., Zobova, N.N. & Balabanova, F.B. Interaction of benzoyl and trichloroacetyl isocyanates with electrophilic reagents. Russ Chem Bull 19, 1479–1482 (1970). https://doi.org/10.1007/BF00853839
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DOI: https://doi.org/10.1007/BF00853839