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Intramolecular radical-induced ring-opening

The cyclopropane ring is cleaved via the induced ring-opening of a cyclopropylcarbinyl radical to form a diradical which in turn cyclizes intramolecularly to afford the reaction product. [Pg.820]

Closing this section on intramolecular epoxide opening, we are also including one case of radical-induced ring fission that may serve very well for the construction of highly substituted cyclopentanes [44]. [Pg.242]

See other pages where Intramolecular radical-induced ring-opening is mentioned: [Pg.515] [Pg.83] [Pg.83] [Pg.140] [Pg.98] [Pg.133] [Pg.265] [Pg.156] [Pg.82] [Pg.192] [Pg.1143] [Pg.98] [Pg.2013] [Pg.41] [Pg.418] [Pg.89]

See also in sourсe #XX -- [ Pg.12 , Pg.83 ]

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Intramolecular opening

Intramolecular radical-induced

Radical ring-opening

Radicals intramolecular

Ring radical