- stereogenic
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b) consisting of a central atom and four distinguishable ligands such that the interchange of any two leads to a stereoisomer
Wikipedia foundation.
Wikipedia foundation.
Chirality (chemistry) — L form redirects here. For the bacterial strains, see L form bacteria. Two enantiomers of a generic amino acid … Wikipedia
isomerism — /uy som euh riz euhm/, n. 1. Chem. the relation of two or more compounds, radicals, or ions that are composed of the same kinds and numbers of atoms but differ from each other in structural arrangement (structural isomerism), as CH3OCH3 and… … Universalium
Monosaccharide — Monosaccharides (from Greek monos: single, sacchar: sugar) are the most basic units of biologically important carbohydrates. They are the simplest form of sugar and are usually colorless, water soluble, crystalline solids. Some monosaccharides… … Wikipedia
Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by … Wikipedia
Epoxide — A generic epoxide. An epoxide is a cyclic ether with three ring atoms. This ring approximately defines an equilateral triangle, which makes it highly strained. The strained ring makes epoxides more reactive than other ethers. Simple epoxides are… … Wikipedia
Stereocenter — A stereocenter or stereogenic center is an atom, bearing groups such that an interchanging of any two groups leads to a stereoisomer.[1] A chirality center is a stereocenter consisting of an atom holding a set of ligands (atoms or groups of… … Wikipedia
Quinine total synthesis — In total synthesis, the Quinine total synthesis describes the efforts in synthesis of quinine over a 150 year period. The development of synthetic quinine is considered a milestone in organic chemistry although it has never been produced… … Wikipedia
stereogenicity — noun The condition of being stereogenic, or of having a stereogenic grouping of atoms … Wiktionary
Chemical glycosylation — A chemical glycosylation reaction involves the coupling of a sugar to a glycosyl acceptor forming a glycoside.[1][2][3] If the acceptor is another sugar, the product is an oligosaccharide. The reaction involves coupling a glycosyl donor to a… … Wikipedia
Ziegler–Natta catalyst — A Ziegler–Natta catalyst is a catalyst used in the synthesis of polymers of 1 alkenes (α olefins). Three types of Ziegler–Natta catalysts are currently employed: Solid and supported catalysts based on titanium compounds. They are used in… … Wikipedia