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Heterocyclization of thiol esters ofα-aminocarboxylic acids with the formation of 5-alkylthio-Δ4-1,3,2-oxazaphospholines

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Abstract

The phosphorylation of the hydrochloride salt of S-butyl N-tert-butylaminothioacetate using phosphorus chlorides in the presence of triethylamine gave a new type of 1,3,2-oxazaphospholines with an alkylthio group at C5 in the oxazaphospholine ring.

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Literature cited

  1. Yu. G. Gololobov and Yu. V. Balitskii, Zh. Obshch. Khim.,44, No. 10, 2356 (1974).

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  3. Yu. G. Gololobov and L. I. Kruglik, Zh. Org. Khim.,17, No. 4, 869 (1981).

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow

    Yu. G. Gololobov & L. I. Kruglik

  2. Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, Kiev

    Yu. G. Gololobov & L. I. Kruglik

Authors
  1. Yu. G. Gololobov
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  2. L. I. Kruglik
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1646–1647, July, 1990.

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Gololobov, Y.G., Kruglik, L.I. Heterocyclization of thiol esters ofα-aminocarboxylic acids with the formation of 5-alkylthio-Δ4-1,3,2-oxazaphospholines. Russ Chem Bull 39, 1495–1496 (1990). https://doi.org/10.1007/BF00957870

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  • DOI: https://doi.org/10.1007/BF00957870

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