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  2. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Absolute configuration uses a set of rules to describe the relative positions of each bond around the chiral center atom. The most common labeling method uses the descriptors R or S and is based on the Cahn–IngoldPrelog priority rules. R and S refer to rectus and sinister, Latin for right and left, respectively.

  3. Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/CahnIngoldPrelog...

    For double bonded molecules, Cahn–IngoldPrelog priority rules (CIP rules) are followed to determine the priority of substituents of the double bond. If both of the high priority groups are on the same side of the double bond (cis configuration), then the stereoisomer is assigned the configuration Z (zusammen, German word meaning "together").

  4. E–Z notation - Wikipedia

    en.wikipedia.org/wiki/E–Z_notation

    Alitretinoin. For organic molecules with multiple double bonds, it is sometimes necessary to indicate the alkene location for each E or Z symbol. For example, the chemical name of alitretinoin is (2E,4E,6Z,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenoic acid, indicating that the alkenes starting at positions 2, 4, and 8 are E while the one starting at position 6 is Z.

  5. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    The designations are based on the same Cahn–IngoldPrelog priority rules used for tetrahedral stereocenters. [3] The chiral axis is viewed end-on and the two "near" and two "far" substituents on the axial unit are ranked, but with the additional rule that the two near substituents have higher priority than the far ones. [4]

  6. Atropisomer - Wikipedia

    en.wikipedia.org/wiki/Atropisomer

    Alternately, all four groups can be ranked by Cahn–IngoldPrelog priority rules, with overall priority given to the two groups on the "front" atom of the Newman projection. The two configurations determined in this way are termed R a and S a, in analogy to the traditional R/S for a traditional tetrahedral stereocenter. [12]

  7. Robert Sidney Cahn - Wikipedia

    en.wikipedia.org/wiki/Robert_Sidney_Cahn

    Robert Sidney Cahn (9 June 1899 – 15 June 1981) was a British chemist, best known for his contributions to chemical nomenclature and stereochemistry, particularly by the Cahn–IngoldPrelog priority rules, which he proposed in 1956 with Christopher Kelk Ingold and Vladimir Prelog. [1] Cahn was the first to report the structure of ...

  8. Vladimir Prelog - Wikipedia

    en.wikipedia.org/wiki/Vladimir_Prelog

    Vladimir Prelog ForMemRS [1] (23 July 1906 – 7 January 1998) was a Croatian-Swiss organic chemist who received the 1975 Nobel Prize in chemistry for his research into the stereochemistry of organic molecules and reactions. Prelog was born, and spent his infancy, in Sarajevo, and youth in Zagreb, Osijek and Prague. [3]

  9. Prochirality - Wikipedia

    en.wikipedia.org/wiki/Prochirality

    A face is labeled re if, when looking at that face, the substituents at the trigonal atom are arranged in increasing Cahn-Ingold-Prelog priority order (1 to 2 to 3) in a clockwise order, and si if the priorities increase in anti-clockwise order; note that the designation of the resulting chiral center as S or R depends on the priority of the ...

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