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Title: Telemerization of alkane- and arenesulfonamides with butadiene catalyzed by palladium complexes

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00951283· OSTI ID:7059721

The authors continue research on the telomerization of 1,3-dienes with compounds that contain labile H atoms by investigating the reaction of butadiene with alkane- and arenesulfonamides under the influence of a catalyst of the Pd-Ln type, which is widely used in processes involving the telomerization of conjugated 1,3-dienes. The expected telomerization products, viz., N-substituted unsaturated sulfonamides, could be of interest for the synthesis of new effective antimicrobial preparations and complexing agents. The catalyzed (by palladium complexes) telomerization of butadiene was realized with butane- and p-toluenesulfonamides, which leads to difficult-to-obtain N-substituted unsaturated sulfoamides in high yields.

Research Organization:
Institute of Chemistry, Bashkir Branch, Acad. of Sci., Ufa
OSTI ID:
7059721
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Vol. 34:2,PT.2
Country of Publication:
United States
Language:
English