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Ozonization of alcohol

Ozonization of polyethylene

Ozonolysis allows the cleavage of alkene double bonds. According to the Criegee mechanism the primary ozonide . Depending on the work-up, different products may be isolated. Oxidative work-up with hydrogen peroxide leads to carboxylic acids ketones, while reductive work-up with either dimethyl sulfide or sodium borohydride gives aldehydes ketones or alcohols, respectively

Ozonolysis of 3-methyl-2-pentene.

Ozonolysis of a styryl-substituted triarylaniine transport molecule.

Ozonolysis of alkene linkers to give aldehydes

Ozonolysis of an alkene.

Ozonolysis of castor oil, followed by reduction and hydrolysis

Ozonolysis of cyclopentadiene

Ozonolysis of stigmastadienone in methylene chloride

Ozonolysis of trifluoromethyluracils

Ozonolysis ofthioanisole .

Ozonolysis products from butadiene containing 11 vinyl structures

Ozonolysis products from PBD containing 11 vinyl structure 4-octene, 1,8 dial. Source

Ozonolysis products from PBD containing 37.2 vinyl structure 4-octene-l,8 dial. Source

Ozonolysis products from polybutadiene containing 11 vinyl structures

Ozonolysis products from polybutadiene containing 37.2 vinyl structure

Ozonolysis products from polybutadiene containing 37.2 vinyl structure. Source

Ozonolysis reaction mechanism, in nonparticipating soivents, the carbonyi oxide are formed in protic soivents, and R can be aikyi or acyi.

Ozonolysis Reactions

Ozonolysis reactions of .

Ozonolysis-SEC curves of copolymer samples at various conversions for styrene butadiene 19.6

Ozonotysis of a phenyl ring.

OZzgoarylenes by Suzuki coupling and synthesis of unsymmetrical biaryl ketones by Pd-catalyzed carbonylation

O— H potential energy curves for 0—H-0 hydrogen bonds



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