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Singlet oxygen carbonyl 1,1 dipole

Wasserman s group showcased the synthetic utility of singlet oxygen cleavage of oxazoles, whereby the oxazole effectively functions as a carbonyl 1,1-dipole. The researchers prepared small and medium rings and applied this methodology to natural product syntheses, including antimycin A3 722 and ( )-pyrenolide C... [Pg.156]


See other pages where Singlet oxygen carbonyl 1,1 dipole is mentioned: [Pg.400]    [Pg.201]    [Pg.366]    [Pg.753]    [Pg.112]    [Pg.90]    [Pg.72]    [Pg.1116]    [Pg.313]    [Pg.241]    [Pg.753]    [Pg.85]   
See also in sourсe #XX -- [ Pg.156 ]




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Carbonyl oxygen

Oxygenation singlet oxygen

Singlet oxygen

Singlet oxygenation

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