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Pericyclic reactions stereochemical changes

As pericyclic reactions are largely unaffected by polar reagents, solvent changes, radical initiators, etc., the only means of influencing them is thermally or photochemically. It is a significant feature of pericyclic reactions that these two influences often effect markedly different results, either in terms of whether a reaction can be induced to proceed readily (or at all), or in terms of the stereochemical course that it then follows. Thus the Diels-Alder reaction (cf. above), an example of a cycloaddition process, can normally be induced thermally but not photochemically, while the cycloaddition of two molecules of alkene, e.g. (4) to form a cyclobutane (5),... [Pg.341]

SCHEME 1.1 Stereochemical changes in pericyclic reactions under thermal and photochemical conditions. [Pg.3]


See other pages where Pericyclic reactions stereochemical changes is mentioned: [Pg.42]    [Pg.40]    [Pg.72]   
See also in sourсe #XX -- [ Pg.2 ]




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Changes Reaction

Pericyclic

Pericyclic reactions

Stereochemical change

Stereochemical reactions

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