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... active ?-siloxy aldehydes are easily available through Sharpless epoxidation of allylic alcohols, followed by ... Highly Regio- and Stereoselective Rearrangement of Epoxides to Aldehydes Catalyzed by High-Valent Metalloporphyrin Complex ...
URL: https://www.organic-chemistry.org/abstracts/literature/257.shtm
... are of course easily prepared using a Sharpless asymmetric epoxidation . Treatment of the chloro ... synthesis of the starting materials, ?-chloro epoxides, which are of course easily prepared ...
URL: https://www.organic-chemistry.org/totalsynthesis/totsyn04/pestalotiopsin-a-tadano.shtm
... 3, the authors took advantage of Sharpless asymmetric epoxidation . To this end, ... acetate 7 was oxidized with SeO2 to the allylic alcohol 8. Epoxidation gave 9 ...
URL: https://www.organic-chemistry.org/Highlights/2017/03April.shtm
... . DOI: 10.1016/j.tetlet.2011.11.145) Sharpless epoxidation , to prepare 5, with ... /ol202190b) 4 by opening the epoxide 1 to the carbene, which cyclized ...
URL: https://www.organic-chemistry.org/Highlights/2012/31December.shtm
... with TBAF gave the alkyne 5. Sharpless asymmetric dihydroxylation followed by selective monomesylation delivered ... epoxide 6, that was cyclized, then protected, leading to the bromoalkene 7 ...
URL: https://www.organic-chemistry.org/Highlights/2021/06September.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: https://www.organic-chemistry.org/Highlights/2004/01November.shtm
... from the simple precursor 30 by sequential Sharpless asymmetric epoxidation and Sharpless asymmetric dihydroxylation ( ... conditions to redirect the cyclization of the epoxide 19 from the expected exo product to ...
URL: https://www.organic-chemistry.org/Highlights/2022/10January.shtm
... to terminal olefins from prim-alcohols (the Grieco-Sharpless olefination reaction) and to the regioselective ... : CATALYTIC ASYMMETRIC DIHYDROXYLATION Original Syntheses of Epoxides Involving Organoselenium Intermediates. A. Krief ...
URL: https://www.organic-chemistry.org/abstracts/authors/krief-a.shtm
... one of the most valuable, is Sharpless asymmetric epoxidation . Karl Anker Jørgensen of ... University, Denmark, devised (J . Am. Chem. Soc. 2005 ...
URL: https://www.organic-chemistry.org/Highlights/2007/26February.shtm
... The diol stereochemistry was unsurprisingly installed using Sharpless' chemistry - in this case a ... asymmetric epoxidation, followed by opening of the allylic epoxide to install the amine. ...
URL: https://www.organic-chemistry.org/totalsynthesis/totsyn06/loline-trauner.shtm
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