The lercanidipine molecule has got one asymmetric carbon atom.
2.
He developed the Fischer projection, a symbolic way of drawing asymmetric carbon atoms.
3.
Because they have at least one asymmetric carbon center, aldoses with three or more carbon atoms exhibit stereoisomerism.
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The " R " conformation of the asymmetric carbon atom seems to be essential for GR affinity.
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The aldotetroses have two chiral centers ( " asymmetric carbon atoms " ) and so 4 different stereoisomers are possible.
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The feature that is most often the cause of chirality in molecules is the presence of an asymmetric carbon atom.
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The asymmetric carbon atom is the one attached to two carbon atoms, an oxygen atom, and a hydrogen atom.
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The 2, 3-dimercaptosuccinic acid molecule has two stereocentres ( two asymmetric carbons ), and can exist as three different stereoisomers.
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An asymmetric carbon is a Stereocenter, an atom that if one group is switched in its arrangement in space a new stereoisomer form.
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Chiral behavior is introduced by inserting asymmetric carbon atom into the mesogenic molecule, termed now smectic C * ( the asterix denotes the chirality ).
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