vicinal diol
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Diol — Ethylene glycol, a simple diol Resorcinol … Wikipedia
Diol — L éthylène glycol, un diol simple. La résorcine … Wikipédia en Français
Pinacol coupling reaction — A pinacol coupling reaction is an organic reaction in which a carbon carbon covalent bond is formed between the carbonyl groups of an aldehyde or a ketone in presence of an electron donor in a free radical process Ref|1. The reaction product is a … Wikipedia
Osmium tetroxide — Osmium tetroxide … Wikipedia
Nicolaou Taxol total synthesis — overview from raw material perspective. The Nicolaou Taxol total synthesis, published by K. C. Nicolaou and his group in 1994 concerns the total synthesis of Taxol. This organic synthesis was included in Nicolaou s book, Classics in Total… … Wikipedia
Upjohn dihydroxylation — is an organic reaction converting an alkene to a cis vicinal diol, and was developed by V. VanRheenen, R. C. Kelly and D. Y. Cha of the Upjohn Company, USA in 1976. [V. VanRheenen, R. C. Kelly and D. Y. Cha Tetrahedron Lett. 1976, 1973 1976.… … Wikipedia
2-Iodoxybenzoic acid — Chembox new ImageFile = IBXAcid.png ImageSize = ImageFileL1 = 2 iodoxybenzoic acid 3D balls.png ImageFileR1 = 2 iodoxybenzoic acid 3D vdW.png IUPACName = OtherNames = IBX Section1 = Chembox Identifiers CASNo = 61717 82 6 PubChem = SMILES =… … Wikipedia
Sharpless asymmetric dihydroxylation — (also called the Sharpless bishydroxylation) is the chemical reaction of an alkene with osmium tetroxide in the presence of a chiral quinine ligand to form a vicinal diol.[1][2][3] … Wikipedia
Glycol cleavage — is a specific type of organic chemistry oxidation. The carbon–carbon bond in a (vicinal diol (glycol) is cleaved and replaced with two carbon–oxygen double bonds. Depending on the substitution pattern in the diol, either ketones or aldehydes may… … Wikipedia
Ruthenium tetroxide — IUPAC name Ruthenium(VIII) oxide … Wikipedia
