stereoselectively

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  • Asymmetric synthesis — Asymmetric synthesis, also called chiral synthesis, enantioselective synthesis or stereoselective synthesis, is organic synthesis which introduces one or more new and desired elements of chirality. [GoldBookRef|title=asymmetric synthesis| file =… …   Wikipedia

  • Alkyne metathesis — is an organic reaction involving the redistribution of alkyne chemical bonds. [ Alkyne metathesis Alois Fürstner and Paul W. Davies, Chemical Communications, 2005, (18), 2307 2320. doi|10.1039/b419143a] This reaction is closely related to olefin… …   Wikipedia

  • Resorcinarene — A resorcinarene (also resorcarene or calix [4] resorcinarene) is a macrocycle, or a cyclic oligomer, based on the condensation of resorcinol (1,3 dihydroxybenzene) and an aldehyde. Resorcinarenes are a type of calixarene. ynthesisThe… …   Wikipedia

  • Enantioselective synthesis — Enantioselective synthesis: Sharpless epoxidation Enantioselective synthesis, also called chiral synthesis, asymmetric synthesis or stereoselective synthesis, is organic synthesis that introduces one or more new and desired elements of… …   Wikipedia

  • Cholesterol total synthesis — Cholesterol Cholesterol space filling model …   Wikipedia

  • Corey-Itsuno reduction — The Corey Itsuno Reduction, also known as the Corey Bakshi Shibata (CBS) reduction, is a chemical reaction in which an achiral ketone is enantioselectively reduced to produce the corresponding chiral, non racemic alcohol. The oxazaborolidine… …   Wikipedia

  • Pancratistatin — Not to be confused with Pancreastatin. Pancratistatin Systematic (IUPAC) name (1R,2S,3S,4S,4aR,11bR) 1,2,3,4,7 pentahydroxy 2,3,4,4a,5,11b hexahydro 1H [1,3]dioxolo[4,5 j]phenanthridin 6 one …   Wikipedia

  • Carbohydrate synthesis — is a sub field of organic chemistry concerned specifically with the generation of natural and unnatural carbohydrate structures. This can include the synthesis of monosaccharide residues or structures containing more than one monosaccharide,… …   Wikipedia

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