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  • An organic [[acid]] with [[antioxidant]] properties whose L-[[enantiomer]] is called vitamin C.
    131 bytes (16 words) - 00:42, 14 July 2008
  • ...{#ifexist:Template:Trans-2,3-dimethyloxirane DEVolk.jpg/credit|<br/>|}}One enantiomer of ''trans''-2,3-dimethyloxirane.]] ...rans-2,3-dimethyl oxirane. The acid-catalyzed ring-opening of the oxirane enantiomer shown here produces (2''S'',3''R'')-3-bromo-2-butanol. Oxirane rings can a
    4 KB (546 words) - 17:14, 31 October 2010
  • {{r|Enantiomer}}
    2 KB (265 words) - 10:53, 11 January 2010
  • The simplest example of an enantiomer is an atom bound to four different substituents. Consider the isomeric str
    2 KB (355 words) - 07:57, 8 June 2009
  • {{r|Enantiomer}}
    4 KB (486 words) - 19:46, 11 January 2010
  • Escitalopram is the S-enantiomer of racemic [[citalopram]].<ref name="pmid19370639">{{cite journal| author=C
    4 KB (501 words) - 13:18, 2 February 2023
  • ...der (from light yellow to brown if oxidized). It is water soluble. The L-[[enantiomer]] of ascorbic acid is commonly known as [[vitamin C]], CASNo = 50-81-7. The [[Optical isomerism|L-enantiomer]] of ascorbic acid is also known as [[vitamin C]]. The name "ascorbic" com
    13 KB (1,893 words) - 10:07, 28 February 2024
  • Additionally, the ribose must all be the same [[enantiomer]], because any nucleotides of the wrong [[chirality (chemistry)|chirality]]
    11 KB (1,710 words) - 11:11, 14 November 2007
  • ...nd experimental investigations have helped to delineate models for how one enantiomer might have come to dominate over the other from what presumably was a racem
    17 KB (2,563 words) - 15:36, 28 June 2012
  • * [[Enantiomer]]
    25 KB (3,396 words) - 13:29, 2 April 2024