• In the industrially important Wacker process, ethylene is converted to acetaldehyde via nucleophilic attack of hydroxide on a Pd(II)-ethylene intermediate followed by formation of a vinyl alcohol complex. (wikipedia.org)
  • The nucleophilic addition between indoles with vinylene carbonate proceeded smoothly in the presence of K2CO3 as the catalyst to produce novel indolyl-containing skeletons and 4-indolyl-1,3-dioxolanones in satisfactory to excellent yields (up to >97% yield). (bvsalud.org)
  • Allyl compounds with suitable leaving groups react with palladium(II) salts to pi-allyl complexes having hapticity 3. (wikipedia.org)
  • Various organic groups can bound to palladium and form stable sigma-bonded complexes. (wikipedia.org)
  • Uses of 2-Deoxy-D-ribose: it can be used to produce lithium 2-deoxy-D-erythro-pentonate at temperature of 40 °C. This reaction will need reagent 3 M KOH, 30 percent H 2 O 2 , MgO, 0.1 M LiOH with reaction time of 18 hours. (lookchem.com)
  • A cooperative catalytic process through Palladium and Brønsted acid activation has been developed for the conjugate addition of cyclic ß -keto esters 2 to azoalkenes 1 directly followed by hemiaminal formation upon cyclization. (uni-leipzig.de)
  • This process involves the formation of a palladium-carbon covalent bond. (wikipedia.org)
  • 1956 - In the Wacker process ethylene and oxygen react to acetaldehyde with catalyst PdCl2/CuCl2 1957 - Tetrakis(triphenylphosphine)palladium(0) is reported by Malatesta and Angoletta. (wikipedia.org)
  • Palladium(II) acetate and related compounds are common reagents because the carboxylates are good leaving groups with basic properties. (wikipedia.org)
  • This chemistry forms the basis of a large class of organic reactions called coupling reactions (see palladium-catalyzed coupling reactions). (wikipedia.org)
  • 1,3-Oxathiolan-5-ones are a hitherto very poorly studied class of sulfur heterocycles some of which have been shown to be important precursors for HIV drugs or bioactive, anticarcinogenic compounds. (uni-leipzig.de)
  • Organopalladium chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions. (wikipedia.org)
  • Palladium(II) acetate and related compounds are common reagents because the carboxylates are good leaving groups with basic properties. (wikipedia.org)
  • Allyl compounds with suitable leaving groups react with palladium(II) salts to pi-allyl complexes having hapticity 3. (wikipedia.org)
  • Zerovalent Pd(0) compounds include tris(dibenzylideneacetone)dipalladium(0) and tetrakis(triphenylphosphine)palladium(0). (wikipedia.org)
  • Palladium compounds owe their reactivity to the ease of interconversion between Pd(0) and palladium(II) intermediates. (wikipedia.org)
  • The compounds associated with a positive aroma were trimethyl orthoacetate, styrene, tridecan-7-amine and acetaldehyde, while compounds related to B. cinerea were hepten-2-one and butanoic acid. (bvsalud.org)
  • Various organic groups can bound to palladium and form stable sigma-bonded complexes. (wikipedia.org)
  • In the reaction of 1,3-dienylboronic esters with nitrosoarenes, a one-pot hetero-Diels-Alder/ring contraction cascade affords N -arylpyrroles with low to good yields depending on the electronic properties of the substituents on the borodiene, whereas an sp 3 boron substituent led to the formation of stable boro-oxazines with high regioselectivity. (organic-chemistry.org)
  • This process involves the formation of a palladium-carbon covalent bond. (wikipedia.org)
  • In the industrially important Wacker process, ethylene is converted to acetaldehyde via nucleophilic attack of hydroxide on a Pd(II)-ethylene intermediate followed by formation of a vinyl alcohol complex. (wikipedia.org)