Conclusions
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1.
The reaction of phenylmercuric hydroxide with a series of cyclic-N-acids and sulfamides was investigated.
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2.
The compounds mentioned above, in contrast to the noncyclic analogs studied earlier with a conformation stabilized by conjugation, form C6H5Hg derivatives.
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3.
Steric hindrances, created by groups whose conformation is not immobilized by resonance, do not hinder the formation of phenylmercuric derivatives of the N-acids.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1741–1747, August, 1967.
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Kravtsov, D.N., Nesmeyanov, A.N. The effect of spatial factors on the reaction of arylmercuric hydroxides with N-acids. Russ Chem Bull 16, 1674–1678 (1967). https://doi.org/10.1007/BF00906811
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DOI: https://doi.org/10.1007/BF00906811