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Further points on correct terminology

In this section we draw attention to several common errors in terminology relating to asymmetric synthesis. [Pg.30]

The first point, which should be obvious to most readers, is that a tetrahedral centre is properly represented by (22) in which the [Pg.30]

A second area concerns the use of the word chiral. This has a specific definition and can only be properly applied to three-dimensional objects. Thus it is incorrect to refer to a chiral centre/axis or a chiral synthesis . The former can be a chirality centre/axis or a centre/axis of chirality although for most purposes we prefer to replace these terms by stereogenic centre/axis (which is, however, not equivalent). [51 As a collective term for enantio- and diastereoselective [Pg.30]

It is important to realise that chirality is a symmetry property of a whole molecule and cannot be localised in a particular centre or group (although it may be associated with the presence of a particular stereogenic unit). For this reason the intramolecular transfer of chirality is an impossibility. Transfer of chirality can only occur between two molecules and is quite uncommon. [An example is the enantioselective Meerwein-Ponndorf-Verley reduction of a ketone with a chiral alcohol.] What some authors refer to incorrectly as transfer of chirality is, in fact, retention of chirality in the course of modification of the stereogenic units present. [Pg.31]


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