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- In stereochemistry, a chiral auxiliary is a stereogenic group or unit that is temporarily incorporated into an organic compound in order to control the...34 KB (3,692 words) - 07:36, 24 August 2023
- Enantioselective synthesis (redirect from Chiral ligand)synthesis. The chiral metal catalysts are almost invariably rendered chiral by using chiral ligands, but it is possible to generate chiral-at-metal complexes...41 KB (4,726 words) - 05:21, 27 May 2024
- Asymmetric hydrogenation (redirect from Bifunctional catalyst)from other reagents or catalysts present in the reaction. This allows spatial information (what chemists refer to as chirality) to transfer from one molecule...64 KB (6,355 words) - 11:56, 3 June 2024
- Enantiomer (redirect from Chiral amplification)In the absence of an effective enantiomeric environment (precursor, chiral catalyst, or kinetic resolution), separation of a racemic mixture into its enantiomeric...24 KB (2,625 words) - 20:09, 14 July 2024
- can be effected using thiourea-derived catalysts. In 2012, a BINOL-derived catalyst was employed to generate chiral cyanide anion (see figure). The German...10 KB (1,069 words) - 08:57, 10 June 2024
- reaction with a chiral catalyst or reagent, resulting in an enantioenriched sample of the less reactive enantiomer. As opposed to chiral resolution, kinetic...57 KB (6,914 words) - 02:14, 2 April 2024
- resolution, in which a pre-existing chiral center undergoes reaction with a chiral catalyst, an enzyme or a chiral reagent such that one enantiomer reacts...8 KB (1,006 words) - 18:00, 19 January 2024
- the active catalyst is not known, Corey’s model proposes the following: the aldehyde is activated by complexation with the chiral catalyst (R)-BINOL-TiX2...27 KB (3,345 words) - 17:19, 18 June 2024
- A variety of chiral thiourea catalysts are under investigation for asymmetric MBH reactions. Chiral thiourea and bis(thiourea) catalysts can be effective...24 KB (2,788 words) - 08:17, 15 June 2024
- reagents. Without a chiral influence (for example a chiral catalyst, solvent or starting material), a chemical reaction that makes a chiral product will always...15 KB (1,824 words) - 07:47, 18 April 2024
- 1021/ar960061v. PMID 10891060. Yoon, TP; Jacobsen, EN (2003). "Privileged Chiral Catalysts". Science. 299 (5613): 1691–1693. doi:10.1126/science.1083622. PMID 12637734...12 KB (1,217 words) - 09:24, 11 April 2024
- Organocatalysis (redirect from McMillan catalyst)acids have been used as catalyst for the modification of cellulose in water on multi-ton scale. When the organocatalyst is chiral an avenue is opened to...17 KB (1,720 words) - 11:46, 11 May 2024
- "interiors" containing the ion and a hydrophobic exterior. Chiral phase-transfer catalysts have also been demonstrated. PTC is widely exploited industrially...7 KB (771 words) - 00:35, 29 January 2024
- enantiopurity of the catalyst or chiral auxiliary does not correspond with the enantiopurity of the product produced. For example: a racemic catalyst would be expected...24 KB (3,183 words) - 07:01, 30 August 2022
- Such chiral diols are important in organic synthesis. The introduction of chirality into nonchiral reactants through usage of chiral catalysts is an...20 KB (2,189 words) - 00:23, 15 July 2024
- may be hydrogenated with low enantioselectivity in the presence of a chiral catalyst. Additionally, the substituent attached to nitrogen affects both the...8 KB (1,016 words) - 00:16, 14 November 2023
- Proline, a naturally occurring chiral compound, is readily and cheaply available. It transfers its stereocenter to the catalyst which in turn is able to drive...4 KB (434 words) - 03:48, 24 December 2023
- product might deactivate the catalyst. Acyclic imines have E/Z isomers. This makes it difficult to create enantiopure chiral compounds through stereoselective...21 KB (2,134 words) - 00:28, 26 May 2024
- mechanisms of each of these reactions differ somewhat, in each case the chiral catalyst or reagent must be involved in the enantio determining conjugate addition...14 KB (1,634 words) - 16:11, 7 March 2021
- or nucleic acids—they like to use asymmetric catalysis, in which a chiral catalyst selectively accelerates the reaction that leads to one mirror-image
- unmodified aldehyde was carried with (S)-proline as a naturally occurring chiral catalyst. The reaction taking place is between a simple aldehyde such as propionaldehyde