chiral

This is due to the extra chiral center at C-2.

This is one of the several techniques used in chiral synthesis.

This was the first time anyone had demonstrated chiral molecules.

This happens when we have a chiral anomaly, for example.

It can also be used for the separation of chiral compounds.

This is a very good way to create new chiral centres.

For chiral objects it is the same as the full symmetry group.

It also means that the sulfur can be a chiral centre.

For that reason, it is sometimes referred to as a "chiral probe."

There is no bare mass term because of the chiral symmetry.

The chiral environment needs not be optically pure for this effect.

The starting material is often derived from chiral pool synthesis.

Direct estimates of the chiral condensate also come from such analysis.

This evidently will have consequences to the chiral dynamics of the theory.

A drug based on just one chiral form or the other is described as optically pure.

With two chiral centres, you can form 4 different isomers.

The re face will simply hit the chiral fence.

These would have been strictly massless in the chiral limit.

All of those sites are chiral themselves - empty gloves waiting for the hand that fits.

The transformations of both parts under a chiral symmetry do not cancel in general.

Still other enzymes produce new chiral centers, always with a high specificity.

For instance, the Standard Model is a chiral gauge theory.

Until 1951 it was not possible to obtain the absolute configuration of chiral compounds.

Since this depends on a choice of orientation, curl is a chiral operation.

Of the remaining 17, five have mirror symmetry, and the other 12 form six chiral pairs.