Chemistry of Heterocyclic Compounds p. 728 - 733 (1984)
Update date:2022-08-03
Topics:
Klimenko, S. K.
Stolbova, T. V.
Tyrina, T. I.
Sorokin, N. N.
Leshcheva, I. F.
et al.
The structure of aryl-substituted cis-1-thiadecalins formed together with 5,6-tetramethylenethiopyrylium salts in disproportionation reactions of condensed 4H-, 6H-thiopyrans and dihydrothiopyrans with CF3COOH, as well as in the ionic reduction of the latter by the ion pair trifluoroacetic acid-triethylsilane, was studied.It was shown that the reduction proceeds stereospecifically with the formation of configurationally and conformationally homogeneous aryl-cis-1-thiadecalins possessing 2α-R1- and 2α-R1-4α-R2-configurations.The configurational and conformational assignments were made by the 13C NMR method.
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