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Cycloadditions 1,3-dienes, photooxygenation

Singlet molecular oxygen (lC>2) is a very small electrophilic reagent that can produced by photosensitization and react easily with dienes and alkenes in [4 + or [2 + 2] cycloadditions or ene-reactions. In order to develop synthetic applic tions of photooxygenations, numerous studies have recently been developed wi chiral substrates and especially in the presence of chiral auxiliaries. [Pg.220]

See other pages where Cycloadditions 1,3-dienes, photooxygenation is mentioned: [Pg.1456]    [Pg.126]    [Pg.211]    [Pg.253]    [Pg.255]    [Pg.256]    [Pg.259]    [Pg.260]    [Pg.262]    [Pg.262]    [Pg.263]    [Pg.858]    [Pg.1448]    [Pg.211]    [Pg.253]    [Pg.255]    [Pg.256]    [Pg.259]    [Pg.259]    [Pg.260]    [Pg.262]    [Pg.262]    [Pg.263]    [Pg.858]    [Pg.167]    [Pg.274]    [Pg.212]    [Pg.348]    [Pg.162]    [Pg.140]    [Pg.149]    [Pg.504]    [Pg.511]    [Pg.516]    [Pg.2224]   
See also in sourсe #XX -- [ Pg.13 ]



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1,3-Dienes, photooxygenation

Diene Cycloaddition

Dienes 3-1-4 cycloadditions

Dienes cycloaddition

Photooxygenation

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