Ozonolysis: Difference between revisions

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[[Ozonolysis]] is a type of [[cycloaddition]] which destroys bonds. It starts with a 1,3-dipolar cycloaddition but eventually becomes a method of cleaving π bonds in an oxidative fashion, so that they end up as two carbonyl groups. The reagent for this reaction is ozone, O<sub>3</sub>.
[[Ozonolysis]] is a type of [[cycloaddition]] which destroys bonds. It starts with a 1,3-dipolar cycloaddition but eventually becomes a method of cleaving π bonds in an oxidative fashion, so that they end up as two carbonyl groups. The reagent for this reaction is ozone, O<sub>3</sub>.
==Reaction==


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This is <scene name='Ozonolysis/Ozonolysis_step_1/1'>step one</scene> of ozonolysis.

Revision as of 12:52, 27 April 2008

Ozonolysis is a type of cycloaddition which destroys bonds. It starts with a 1,3-dipolar cycloaddition but eventually becomes a method of cleaving π bonds in an oxidative fashion, so that they end up as two carbonyl groups. The reagent for this reaction is ozone, O3.

Reaction

Insert caption here

Drag the structure with the mouse to rotate

This is step one of ozonolysis.

Proteopedia Page Contributors and Editors (what is this?)

Eran Hodis, Eric Martz, Michal Harel