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Conjugated polyenes electrocyclic ring closure

In an electrocyclic reaction, a cyclic system (ring closure) is formed through the formation of a a-bond from an open-chain conjugated polyene system at the cost of a multiple bond and vice versa (ring opening). These reactions are unimolecular in nature as the rate of reactions depends upon the... [Pg.3]

The Diels-Alder reaction couples the ends of two separate tt systems. Can rings be formed by the linkage of the termini of a single conjugated di-, tri-, or polyene Yes, and this section will describe the conditions under which such ring closures (and their reverse), called electrocyclic reactions, take place. Cycloadditions and electrocyclic reactions belong to a class of transformations called pericyclic (peri, Greek, around), because they exhibit transition states with a cyclic array of nuclei and electrons. [Pg.608]

In electrocyclic reactions as already mentioned there is ring-opening or ring-closure of polyenes. In these reactions an open chain conjugated olefinic system with nn-electrons undergoes ring-closure to a system with (n -2) n-electrons + one o-bond and converse of this process is also feasible under changed reaction conditions. Some examples of electrocyclic reactions are cited below ... [Pg.36]


See other pages where Conjugated polyenes electrocyclic ring closure is mentioned: [Pg.56]    [Pg.32]    [Pg.139]    [Pg.198]    [Pg.262]   
See also in sourсe #XX -- [ Pg.231 , Pg.232 , Pg.233 , Pg.234 , Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.247 , Pg.248 ]

See also in sourсe #XX -- [ Pg.231 , Pg.232 , Pg.233 , Pg.234 , Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.247 , Pg.248 ]

See also in sourсe #XX -- [ Pg.231 , Pg.232 , Pg.233 , Pg.234 , Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.247 , Pg.248 ]




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Conjugated polyenes

Conjugated rings

Polyene conjugated

Polyenes conjugation

Ring closure, electrocyclic

Ring electrocyclic

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