Products of Reaction of Tricyclo[4.1.0.02,7]heptane and 1-Bromotricyclo[4.1.0.02,7]heptane with Hydrogen Sulfide,and Syntheses Based Thereon |
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Authors: | Vasin V A Kostryukov S G Razin V V |
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Institution: | (1) Mordovian Ogarev State University, Saransk, 430000, Russia;(2) St. Petersburg State University, St. Petersburg, 198904, Russia |
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Abstract: | By reactions of 1-R-tricyclo4.1.0.02,7]heptanes (R = H, Br) with hydrogen sulfide initiated by UV irradiation endo-6-bicyclo3.1.1]heptanethiols and bis(endo-6-bicyclo3.1.1]heptyl) sulfides were synthesized. The sulfides were oxidized to the corresponding sulfoxides and sulfones. The results of HBr elimination from the bromine-substituted sulfoxides and sulfones effected by potassium tert-butylate are discussed. The latter reaction results in the recovery of the system of 1-substituted tricyclo4.1.0.02,7]heptane. |
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