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Diels-Alder reactions cationic heterodienes

The use of a range of modified reaction conditions including the use of protic acids or conventional and nonconventional Lewis acid catalysts, pressure-promoted reaction conditions, - cation-radical catalysts, and dry-state adsorption reaction conditions has been employed to accelerate the 4it participation of sensitive heterodienes in thermally slow or problematic Diels-Alder reactions. The former two techniques have proven useful for promoting the typically poor reactions of simple, unactivated 1-oxa-1,3-butadienes or acyclic azadienes. [Pg.453]

See other pages where Diels-Alder reactions cationic heterodienes is mentioned: [Pg.156]    [Pg.156]    [Pg.156]   
See also in sourсe #XX -- [ Pg.492 , Pg.493 , Pg.494 , Pg.495 , Pg.496 , Pg.497 , Pg.498 , Pg.499 , Pg.500 , Pg.501 , Pg.502 , Pg.503 , Pg.504 , Pg.505 , Pg.506 ]

See also in sourсe #XX -- [ Pg.5 , Pg.492 , Pg.493 , Pg.494 , Pg.495 , Pg.496 , Pg.497 , Pg.498 , Pg.499 , Pg.500 , Pg.501 , Pg.502 , Pg.503 , Pg.504 , Pg.505 , Pg.506 ]

See also in sourсe #XX -- [ Pg.492 , Pg.493 , Pg.494 , Pg.495 , Pg.496 , Pg.497 , Pg.498 , Pg.499 , Pg.500 , Pg.501 , Pg.502 , Pg.503 , Pg.504 , Pg.505 , Pg.506 ]

See also in sourсe #XX -- [ Pg.5 , Pg.492 , Pg.493 , Pg.494 , Pg.495 , Pg.496 , Pg.497 , Pg.498 , Pg.499 , Pg.500 , Pg.501 , Pg.502 , Pg.503 , Pg.504 , Pg.505 , Pg.506 ]



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Cation Diels-Alder reaction

Cationic reactions

Diels-Alder reactions heterodienes

Heterodiene

Heterodienes

Heterodienes cationic

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