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Search results for: sharpless epoxidation

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... , K. B. Sharpless, Angew. Chem ... FUNCTIONALIZED SECONDARY ALCOHOLS/ASYMMETRIC EPOXIDATION CATALYSTS/DIELS-ALDER REACTION ... /CATALYSIS/DIHYDROXYLATIONS/EPOXIDATIONS/TITANIUM COMPOUNDS/ ...
URL: http://www.organic-chemistry.org/abstracts/authors/berrisford-d-j.shtm
... alcohols such as 12 are prepared by Sharpless asymmetric epoxidation. Kohji Suda of Meiji ... chloro alcohol with high diastereoselectivity. The epoxidation procedure developed by Yian Shi of Colorado ...
URL: http://www.organic-chemistry.org/Highlights/2005/18July.shtm
... one of the most valuable, is Sharpless asymmetric epoxidation. Karl Anker Jørgensen of ... University, Denmark, devised (J. Am. Chem. Soc. 2005 ...
URL: http://www.organic-chemistry.org/Highlights/2007/26February.shtm
... . For more than two decades, Sharpless asymmetric epoxidation of allylic alcohols has been ... workhorse for enantioselective synthesis. Karl Anker Jørgensen of Aarhus University, Denmark, has ...
URL: http://www.organic-chemistry.org/Highlights/2006/13February.shtm
... can be prepared in high ee by Sharpless epoxidation. Norbert Krause of Dortmund University ... shown (Angew. Chem. Int. Ed. 2007, 46, 1650 ...
URL: http://www.organic-chemistry.org/Highlights/2007/19November.shtm
... /SYNTHESIS/TM CATALYSTS/REDUCTION SHARPLESS EPOXIDATION CYCLOPROPANATION DIELS-ALDER ALDOL HYDROGENATION CROSS COUPLING ... /HETRING/3(O)/TM Enantioselective Synthesis of Organic Compounds with ...
URL: http://www.organic-chemistry.org/abstracts/authors/brunner-h.shtm
... to terminal olefins from prim-alcohols (the Grieco-Sharpless olefination reaction) and to the regioselective ... /SELENIUM/SeO2/OXIDATION/EPOXIDATION/Se Transformations of ß-hydroxyalkyl selenides to ...
URL: http://www.organic-chemistry.org/abstracts/authors/krief-a.shtm
... active ?-siloxy aldehydes are easily available through Sharpless epoxidation of allylic alcohols, followed by ... and rearrangement. see article for more examples Key Words Rearrangements, Aldehydes ID: ...
URL: http://www.organic-chemistry.org/abstracts/literature/257.shtm
... using the usual reagents failed, but Sharpless asymmetric dihydroxylation was successful, providing the ... both 1 and 2. Selective direct epoxidation of 11 using the usual reagents failed ...
URL: http://www.organic-chemistry.org/Highlights/2004/01November.shtm
... centers of 2 were then established by Sharpless asymmetric epoxidation. The preparation of the ... 1 began with pulegone 8, available commercially in high enantiomeric purity. Methylation followed ...
URL: http://www.organic-chemistry.org/Highlights/2004/03May.shtm
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