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In stereochemistry, prochiral molecules are those that can be converted from achiral to chiral in a single step. [1] [2] An achiral species which can be converted to a chiral in two steps is called proprochiral. [2] If two identical substituents are attached to an sp 3-hybridized atom, the descriptors pro-R and pro-S are used to distinguish ...
Instead, both effects can also occur when the propagation direction of the electromagnetic wave together with the structure of an (achiral) material form a chiral experimental arrangement. [10] [11] This case, where the mutual arrangement of achiral components forms a chiral (experimental) arrangement, is known as extrinsic chirality. [12] [13]
Proline (symbol Pro or P) [4] is an organic acid classed as a proteinogenic amino acid (used in the biosynthesis of proteins), although it does not contain the amino group-NH 2 but is rather a secondary amine .
If the arrangement is clockwise, it is the D form. As usual, if the molecule itself is oriented differently, for example, with H towards the viewer, the pattern may be reversed. The L form is the usual one found in natural proteins. For most amino acids, the L form corresponds to an S absolute stereochemistry, but is R instead for certain side ...
Extrinsic means that the chirality is a consequence of the arrangement of different components, rather than an intrinsic property of the components themself. For example, the propagation direction of a beam of light through an achiral crystal (or metamaterial) can form an experimental arrangement that is different from its mirror image.
Racemic crystal structure of Rv1738 from Mycobacterium tuberculosis produced by racemic protein crystallography. Racemic crystallography is a technique used in structural biology where crystals of a protein molecule are developed from an equimolar mixture of an L-protein molecule of natural chirality and its D-protein mirror image.
The chiral stationary phase (CSP) is made of a support, usually silica based, on which a chiral reagent or a macromolecule with numerous chiral centers is bonded or immobilized. [3] The chiral stationary phase can be prepared by attaching a chiral compound to the surface of an achiral support such as silica gel.
The chirality of the allymetals usually comes from the asymmetric ligands used. The metals in the allylmetal reagents include boron, tin, titanium, silicon, etc. Fig. 1: Reagent control: addition of chiral allylmetals to achiral aldehydes. Various chiral ligands have been developed to prepare chiral allylmetals for the reaction with aldehydes ...