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Unfunctionalized alkenes, stereoselective cyclopropanation

Allylic alcohols also cyclopropanate over 100 times faster than their unfunctionalized alkene equivalents. Coordination between the zinc atom and the hydroxyl group in the transition state explains both the stereoselectivity and the rate increase. Unfortunately, while the Simmons-Smith... [Pg.1067]


See other pages where Unfunctionalized alkenes, stereoselective cyclopropanation is mentioned: [Pg.146]    [Pg.16]   
See also in sourсe #XX -- [ Pg.276 ]




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Alkenes cyclopropanation

Alkenes stereoselective

Alkenes stereoselectivity

Alkenes unfunctionalized

Cyclopropanation stereoselectivity

Cyclopropanations alkenes

Cyclopropane 3-alken

Cyclopropane alkene

Cyclopropanes stereoselective cyclopropanation

Stereoselective cyclopropanation

Stereoselectivity alkene cyclopropanation

Unfunctionalized alkenes, stereoselective

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