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Chiral symmetry breaking occurs when a physical or chemical process that does not have preference for the production of one or other enantiomer spontaneously generates a large excess of one of the two enantiomers: left-handed (L) or right-handed (D). From the energetic point of view, these two enantiomers can exist with an equal probability and inorganic processes involving chiral products commonly yield a racemic mixture of both (L) and (D) enantiomers [1]. However, life on earth utilizes only one type of amino acids and only one type of natural sugars: (L)-amino acids and (D)-sugars. The fact that biologically relevant molecules exist only as one of the two enantiomers is a fascinating example of complete symmetry breaking in chirality and has long intrigued many scientists.