Carboxylic Acid Silyl Esters, Sulfonic Acid Silyl Esters
Silane carboxylates and silane sulfonates are two common silicon-containing compounds that are widely used in organosilicon chemistry and materials science. They connect silane groups with carboxylic acid or sulfonic acid groups through silicon-oxygen bonds (Si-O) and have important chemical and physical properties. Silane carboxylates and silane sulfonates play important roles in surface modification, polymer synthesis, catalytic reactions, etc. They combine silane groups with functional acid groups (carboxylic acid or sulfonic acid) to form compounds with special properties, which are widely used in materials science, chemical engineering, electronics, coatings and other industries.
Technical Resources
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiralChiral chloro-indeno pybox has served as a new ligand for the Yb(OTf)3-catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with nitroalkenes. The tunable nature of pybox ligands
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2Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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3Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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4Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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5Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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In-stockPurity: 98%(stabilized with BHT)
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In-stockPurity: ≥95%
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In-stockPurity: ≥98%
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In-stockPurity: ≥95%
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In-stockPurity: ≥98%
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In-stockPurity: ≥98%
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