Conclusions
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1.
The reaction of S-alkyl alkyl(aryl)chlorothiophosphonites with propargyl alcohol or with propargyl mercaptan in the presence of a base leads to the formation of S-alkyl alkyl(aryl)allenylthio(dithio)phosphinates, which when heated with a sodium alcoholate are converted to S-alkyl alkyl(aryl)-1-propynylthiophosphinates.
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2.
Alkyl(aryl)dichlorothiophosphites react with propargyl alcohol to give S-alkyl(aryl)allenylchlorothiophosphonates, while the reaction of ethyldichlorophosphine with propargyl mercaptan leads to the formation of ethylallenylchlorothionophosphine.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2755–2758, December, 1973.
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Eliseenkova, R.M., Rizpolozhenskii, N.I. & Akamsin, V.D. Esters of trivalent phosphorus thioacids. Russ Chem Bull 22, 2687–2690 (1973). https://doi.org/10.1007/BF00926138
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DOI: https://doi.org/10.1007/BF00926138