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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
Baeyer–Drewson indigo synthesis; Baeyer–Villiger oxidation, Baeyer–Villiger rearrangement [12]; Bakeland process (Bakelite) Baker–Venkataraman rearrangement, Baker–Venkataraman transformation [13] [14] [15] [16]
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.
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
Organic reactions machine-readable reaction schemes "ORD" [8] 2,000,000 OrgSyn Organic Syntheses: Organic Syntheses, Inc. Reliable chemical reactions Searchable experimental procedures Peer reviewed "OrgSyn search". PDB PDBe Protein Data Bank in Europe EMBL-EBI: has some chemicals as well as proteins "PDBe". PATENTSCOPE: WIPO "PATENTSCOPE ...
The leaving group X in the organic partner is usually a halide, although triflate, tosylate, pivalate esters, and other pseudohalides have been used. [15] Chloride is an ideal group due to the low cost of organochlorine compounds. Frequently, however, C–Cl bonds are too inert, and bromide or iodide leaving groups are required for acceptable ...
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]
Triethyloxonium tetrafluoroborate is the organic oxonium compound with the formula [(CH 3 CH 2) 3 O] + [BF 4] −. It is often called Meerwein's reagent or Meerwein's salt after its discoverer Hans Meerwein. [2] [3] Also well known and commercially available is the related trimethyloxonium tetrafluoroborate. The compounds are white solids that ...