To use all functions of this page, please activate cookies in your browser.
my.chemeurope.com
With an accout for my.chemeurope.com you can always see everything at a glance – and you can configure your own website and individual newsletter.
- My watch list
- My saved searches
- My saved topics
- My newsletter
ProchiralIn chemistry, prochiral molecules can be converted from achiral to chiral in a single step.[1] Additional recommended knowledgeIf two identical substituents are attached to an sp3-hybridized atom, the descriptors pro-R and pro-S are used to distinguish between the two. Replacing the pro-R substituent results in an R chirality center at the original sp3-hybridized atom, and vice versa. A trigonal planar sp2-hybridized atom can be converted to a chirality center when a substituent is added to the re or si face of the molecule.
See alsoReferences
|
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Prochiral". A list of authors is available in Wikipedia. |