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Conjugated dienes sigmatropic shifts

The outcome of all this for photochemical sigmatropic shifts is that those most commonly observed are of order (1.3) or (1.7) these involve 4 or 8 electrons, respectively, and occur in a suprafacial manner. Examples of photochemical 1.3-shifts of hydrogen are found for monoalkenes (2.25) and for conjugated dienes 2.26). In the case of dienes a 1,3-shift is favoured over a 1,5-shift, because for the latter to occur photochemically it would have to take place in an antarafacial manner. Note that in both examples the direction of... [Pg.52]

There are five classes of pericyclic reactions, only two of which are covered in this book, cycloadditions and sigmatropic shifts. The most common, cycloaddition involves the reaction of a conjugated diene with an alkene, although we also examine the reaction of an alkene with an alkene. Hence, we are examining what are commonly called 4 + 2 and 2 + 2 cycloadditions, respectively, to keep track of the number of 77 electrons involved in the reaction. [Pg.878]


See other pages where Conjugated dienes sigmatropic shifts is mentioned: [Pg.732]    [Pg.732]    [Pg.599]    [Pg.905]    [Pg.292]    [Pg.1126]    [Pg.1147]    [Pg.1010]    [Pg.12]    [Pg.789]    [Pg.98]    [Pg.470]    [Pg.789]   
See also in sourсe #XX -- [ Pg.856 , Pg.857 , Pg.858 , Pg.859 , Pg.860 ]




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1,3-Diene, conjugated

Conjugate 1,3 dienes

Conjugation Dienes, conjugated)

Conjugation shifts

Dienes conjugated

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