Cyclization by Intramolecular Addition Reactions

If a radical is joined to a double bond by a chain of three or more carbons intramolecular addition generates a ring. The regioselectivity of such additions is governed more by stereoelectronic factors than by substituents on the double bond. In the first two examples shown below, double bond substitution would favor formation of a six-membered ring, but five-membered ring formation by way of a 1º-cyclized radical dominates the products. Likewise, in reaction 3 a six-membered ring is formed preferentially over an alternative seven-membered ring. In each of the examples the ring forming bond is colored red. . Note that these reactions tolerate a wide variety of functional groups.

The stereoelectronic factor in this reaction is defined by the preferred mode of approach of a radical as it bonds to the pi-electron system of an alkene function. As shown in the following diagram, this is at an angle nearly 20º off the perpendicular to the plane of the double bond. Because of this requirement, many cyclizations to moderately sized rings proceed by radical attack at the nearest carbon of the double bond, regardless of substitution. Bonding to the distal carbon is constrained by the structure of the connecting chain. Of course, if the carbon chain tethering the radical site to the double bond is long enough, bonding to either of the double bond carbons accommodates the stereoelectronic factor, and the product is again determined by substitution.

مواضيع ذات صلة

Oxidation-Reduction of Organic Compounds

Hydrogenation with Heterogeneous Catalysts

Mechanism of Hydrogenation

Catalyst Activity and Selectivity

Hydrogenation with Homogeneous Catalysts

Nucleophilic Addition Reactions

Radical-Chain Addition Reactions to Alkenes

Orientation of Addition

Cationic Polymerization

Radical Polymerization

Coordination Polymerization

Addition of HX