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Search results for: ozonolysis

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... Synthesis of Tetrasubstituted Ozonides by the Griesbaum Coozonolysis Reaction: Diastereoselectivity and Functional Group Transformations ... Post-Ozonolysis Reactions Yuanqing Tang, Yuxiang Dong, Jean M. Karle, Charles A ...
URL: http://www.organic-chemistry.org/abstracts/lit1/016.shtm
... Organic Chemistry Portal Unsymmetrical Ozonolysis of a Diels-Alder Adduct: Practical Preparation of a Key Intermediate for Heme Total Synthesis Douglass F. Taber* and Katsumasa Nakajima * ...
URL: http://www.organic-chemistry.org/abstracts/literature/963.shtm
... Organic Chemistry Portal Osmium Tetroxide-Promoted Catalytic Oxidative Cleavage of Olefins: An Organometallic Ozonolysis Benjamin R. Travis, Radha S. Narayan and Babak Borhan* *Department ...
URL: http://www.organic-chemistry.org/abstracts/literature/040.shtm
... :5 regioselectivity, and in up to 96% ee. In conjunction with ozonolysis, this process allows the enantioselective synthesis of ?-hydroxy ketones. see article for ...
URL: http://www.organic-chemistry.org/abstracts/literature/112.shtm
... oxidation with O 3. see article for more examples Key Words Ullmann Coupling, Ozonolysis, Ozone, Azetidines, ?-Lactams ID: J54-Y2006-3680 ...
URL: http://www.organic-chemistry.org/abstracts/lit1/490.shtm
... 2. The aldehyde 2 was prepared from the inexpensive geraniol ether 5. Selective ozonolysis followed by Wittig homologation gave the bromodiene, which was converted via dehydrobromination and ...
URL: http://www.organic-chemistry.org/Highlights/2004/03May.shtm
... the congested tetrasubstituted alkene, so the more reactive alkene was temporarily epoxidized. After ozonolysis, the epoxide was reduced off using the Sharpless protocol. It is a ...
URL: http://www.organic-chemistry.org/Highlights/2004/04October.shtm
... was cyclized with> 10:1 regio- and diasterocontrol to give 12. Ozonolysis and methylenation of the less hindered ketone then delivered 3. In both of ...
URL: http://www.organic-chemistry.org/Highlights/2004/06December.shtm
... commercially-available 2-methylcyclopentenone, by conjugate addition followed by alkylation of the regenerated ketone enolate. Ozonolysis followed by selective reduction then led to 11. Resolution was accomplished by enantioselective ...
URL: http://www.organic-chemistry.org/Highlights/2004/07June.shtm
... 1487-1493. Link). The key step was the preparation of 16 by a coozonolysis of O-methyl 2-adamantanone oxime with a 4-substituted cyclohexanone. Neurotoxicity in animal models has ...
URL: http://www.organic-chemistry.org/Highlights/2004/25OctoberA.shtm
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