Search results
Results from the WOW.Com Content Network
used as a pigment and as a precursor to other manganese compounds; used as a reagent in organic synthesis for the oxidation of allylic alcohols Meta-Chloroperoxybenzoic acid: used as an oxidant in organic synthesis Methyl tert-butyl ether: a gasoline additive; also used in organic chemistry as a relatively inexpensive solvent Millon's reagent
Collins reagent; Combes quinoline synthesis; Conia reaction; Conrad–Limpach synthesis; Cook–Heilbron thiazole synthesis; Cope elimination; Cope rearrangement [24] Corey reagent; Corey–Bakshi–Shibata reduction; Corey–Fuchs reaction; Corey–Gilman–Ganem oxidation; Corey–Kim oxidation; Corey-Nicolaou macrolactonization
This category was created to provide a "home" for inorganic compounds (such as NaBH 4) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as oxalyl chloride) may belong here also. This category is not for catalysts such as Pd.
The online video game platform and game creation system Roblox has numerous games (officially referred to as "experiences") [1] [2] created by users of its creation tool, Roblox Studio. Due to Roblox ' s popularity, various games created on the site have grown in popularity, with some games having millions of monthly active players and 5,000 ...
2,4,6-Trichlorobenzoyl chloride or Yamaguchi's reagent is an chlorinated aromatic compound that is commonly used in a variety of organic syntheses. [ 2 ] [ 3 ] Yamaguchi esterification
TCFH itself is a common reagent used in the preparation of uronium and guanidinium salts used for amide bond formation and peptide synthesis, such as HATU. [3] [4] [5]Amide bond formation with TCFH can be performed in a wide range of organic solvents, most commonly acetonitrile, but also water [6] and in the solid state. [7]
Other reagents used for alpha-hydroxylation via enol or enolate structures include Davis oxaziridine, oxygen, and various peroxyacids (see Rubottom oxidation). This reagent was first utilized by Edwin Vedejs as an efficient alpha-hydroxylating agent in 1974 and an effective preparative procedure was later published in 1978.
Trimethyloxonium tetrafluoroborate is the organic compound with the formula [(CH 3) 3 O] + [BF 4] −. (It is sometimes called "Meerwein's salt" after Hans Meerwein. [1] [a]) This salt is a strong methylating agent, being a synthetic equivalent of CH + 3. It is a white solid that rapidly decomposes upon exposure to atmospheric moisture ...