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Lactone Annulation and Substitutive Spiroannulation

The facile conversion of carbonyl groups into lactones via cyclobutanones offers many opportunities for synthetic applications considering the importance of butanol-ides in natural products synthesis. The iridoids vividly illustrate this potential. Allamandin (163) 135 c) and its dehydrated relative plumericin (164) 135 d), compounds possessing antifungal, antibacterial, and antitumor activity, pack a great deal of [Pg.68]

At this time, we can focus on the creation of the butenolide. Sulfur based methodoly allows simplification to the simple butanolide as in 170. While cyclobutanone spiroannulation of 171 followed by a Baeyer-Villiger reaction would create 170, [Pg.70]


See other pages where Lactone Annulation and Substitutive Spiroannulation is mentioned: [Pg.9]    [Pg.72]    [Pg.5]    [Pg.68]   


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And lactonization

Lactones annulation

Lactones substituted

Lactones substitution

Spiroannulation

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