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Fischer-Rosanoff convention

With more complex molecules than straight-chain aldoses, particularly those containing tertiary or quaternary chiral centres, the Fischer-Rosanoff convention founders on the impossibility of deciding reliably what is the main chain. [Pg.7]

Fischer-Rosanoff convention A method for the specification of absolute configuration, still in common use for amino acids and sugars. When drawn in a Fischer projection with Ci at the top, if the functional group of the specified stereocenter is on the right, the absolute configuration is D, if on the left, it is L. For amino acids, the reference stereocenter is C2 for sugars it is the highest numbered stereocenter [98],... [Pg.27]


See other pages where Fischer-Rosanoff convention is mentioned: [Pg.208]    [Pg.213]    [Pg.1104]    [Pg.1107]    [Pg.587]    [Pg.2]    [Pg.7]    [Pg.587]    [Pg.208]    [Pg.1100]    [Pg.1103]    [Pg.1142]    [Pg.587]    [Pg.643]    [Pg.643]    [Pg.645]    [Pg.587]    [Pg.208]    [Pg.213]    [Pg.1104]    [Pg.1107]    [Pg.587]    [Pg.2]    [Pg.7]    [Pg.587]    [Pg.208]    [Pg.1100]    [Pg.1103]    [Pg.1142]    [Pg.587]    [Pg.643]    [Pg.643]    [Pg.645]    [Pg.587]    [Pg.97]    [Pg.13]    [Pg.22]    [Pg.26]    [Pg.1092]    [Pg.6]    [Pg.1092]    [Pg.6540]    [Pg.3]    [Pg.25]   
See also in sourсe #XX -- [ Pg.208 , Pg.1104 ]

See also in sourсe #XX -- [ Pg.27 ]

See also in sourсe #XX -- [ Pg.202 , Pg.1100 ]




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Fischer-Rosanoff convention projection

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