The lercanidipine molecule has got one asymmetric carbon atom.
2.
He developed the Fischer projection, a symbolic way of drawing asymmetric carbon atoms.
3.
The " R " conformation of the asymmetric carbon atom seems to be essential for GR affinity.
4.
The aldotetroses have two chiral centers ( " asymmetric carbon atoms " ) and so 4 different stereoisomers are possible.
5.
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.
7.
Chiral behavior is introduced by inserting asymmetric carbon atom into the mesogenic molecule, termed now smectic C * ( the asterix denotes the chirality ).
8.
Three of these alcohols, active amyl alcohol ( 2-methylbutan-1-ol ), methyl ( n ) propyl carbinol ( pentan-2-ol ), and methyl isopropyl carbinol ( 3-methylbutan-2-ol ), contain an asymmetric carbon atom and are therefore optically active.
9.
One may initially be inclined to think this atom is not asymmetric because it is attached to two carbon atoms, but because those two carbon atoms are not attached to exactly the same things, there are two different " groups " of atoms that the carbon atom in question is attached to, therefore making it an asymmetric carbon atom:
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