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- Asymmetric_hydrogenation abstract "Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three-dimensional spatial selectivity. Critically, this selectivity does not come from the target molecule itself, but from other reagents or catalysts present in the reaction. This allows spatial information (what chemists refer to as chirality) to transfer from one molecule to the target, forming the product as a single enantiomer. The chiral information is most commonly contained in a catalyst and, in this case, the information in a single molecule of catalyst may be transferred to many substrate molecules, amplifying the amount of chiral information present. Similar processes occur in nature, where a chiral molecule like an enzyme can catalyse the introduction of a chiral centre to give a product as a single enantiomer, such as amino acids, that a cell needs to function. By imitating this process, chemists can generate many novel synthetic molecules that interact with biological systems in specific ways, leading to new pharmaceutical agents and agrochemicals. The importance of asymmetric hydrogenation in both academia and industry contributed to two of its pioneers — William Standish Knowles and Ryōji Noyori — being awarded one half of the 2001 Nobel Prize in Chemistry.".
- Asymmetric_hydrogenation thumbnail Generic_Asymmetric_Hydrogenation.png?width=300.
- Asymmetric_hydrogenation wikiPageID "19425312".
- Asymmetric_hydrogenation wikiPageRevisionID "599787865".
- Asymmetric_hydrogenation align "right".
- Asymmetric_hydrogenation caption "Effective ligand for various asymmetric-hydrogenation processes".
- Asymmetric_hydrogenation caption "Generic PHOX ligand architecture".
- Asymmetric_hydrogenation hasPhotoCollection Asymmetric_hydrogenation.
- Asymmetric_hydrogenation image "Generic PHOX Ligand.tif".
- Asymmetric_hydrogenation image "PO Ligand Asymmetric Hydrogenation.tif".
- Asymmetric_hydrogenation width "(31.5*3) round 0".
- Asymmetric_hydrogenation width "(48.2*3) round 0".
- Asymmetric_hydrogenation subject Category:Chemical_processes.
- Asymmetric_hydrogenation subject Category:Chemistry.
- Asymmetric_hydrogenation subject Category:Green_chemistry.
- Asymmetric_hydrogenation subject Category:Inorganic_chemistry.
- Asymmetric_hydrogenation subject Category:Matter.
- Asymmetric_hydrogenation subject Category:Organic_chemistry.
- Asymmetric_hydrogenation comment "Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three-dimensional spatial selectivity. Critically, this selectivity does not come from the target molecule itself, but from other reagents or catalysts present in the reaction. This allows spatial information (what chemists refer to as chirality) to transfer from one molecule to the target, forming the product as a single enantiomer.".
- Asymmetric_hydrogenation label "Asymmetric hydrogenation".
- Asymmetric_hydrogenation sameAs m.0n40_yt.
- Asymmetric_hydrogenation sameAs Q4812077.
- Asymmetric_hydrogenation sameAs Q4812077.
- Asymmetric_hydrogenation wasDerivedFrom Asymmetric_hydrogenation?oldid=599787865.
- Asymmetric_hydrogenation depiction Generic_Asymmetric_Hydrogenation.png.
- Asymmetric_hydrogenation isPrimaryTopicOf Asymmetric_hydrogenation.