Telemerization of alkane- and arenesulfonamides with butadiene catalyzed by palladium complexes
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
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Related Subjects
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
BUTADIENE
TELOMERIZATION
PALLADIUM COMPLEXES
CATALYTIC EFFECTS
SULFONAMIDES
CHEMICAL REACTION YIELD
CATALYSTS
ELECTRON SPIN RESONANCE
NMR SPECTRA
STRUCTURAL CHEMICAL ANALYSIS
AMIDES
ANTI-INFECTIVE AGENTS
ANTIMICROBIAL AGENTS
CHEMICAL REACTIONS
COMPLEXES
DIENES
DRUGS
HYDROCARBONS
MAGNETIC RESONANCE
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
POLYENES
POLYMERIZATION
RESONANCE
SPECTRA
TRANSITION ELEMENT COMPLEXES
YIELDS
400201* - Chemical & Physicochemical Properties