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Search results for: "shi epoxidation"

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... , 1997, 119, 11224-11235. Key Words Epoxides , Organocatalysis , Oxone , Shi Epoxidation ID: J42-Y2008-3660 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/365.shtm
... , 2008, 73, 9539-9543. Key Words Epoxides , Organocatalysis , Oxone , Shi Epoxidation ID: J48-Y2000-680 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/370.shtm
... , 2008, 73, 9539-9543. Key Words Epoxides , Organocatalysis , Oxone , Shi Epoxidation ID: J48-Y1997-750 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/368.shtm
... , 2008, 73, 9539-9543. Key Words Epoxides , Organocatalysis , Oxone , Shi Epoxidation ID: J42-Y2007-1590 ...
URL: https://www.organic-chemistry.org/abstracts/lit1/699.shtm
... Lanzhou University used (Org. Lett. 2014, 16, 1996. ) Shi epoxidation and Itsuno-Corey reduction to prepare 18 in enantiomerically-pure form. Cationic cyclization converted ...
URL: https://www.organic-chemistry.org/Highlights/2014/29December.shtm
... nice prepration of this catalyst from natural L-sorbose . The lower d.r. in the Shi epoxidation is maybe a result of a conflict between substrate and reagent control . ...
URL: https://www.organic-chemistry.org/totalsynthesis/totsyn05/omaezakianol-morimoto.shtm
... selectivities. see article for more examples Key Words Epoxides , Organocatalysis , Oxone , Shi Epoxidation ID: J60-Y2008-3500 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/349.shtm
... J . Org. Chem. 2011, 76, 5506. ) 31 by Shi epoxidation. Although several competing reduction products were observed under alternative conditions, they ...
URL: https://www.organic-chemistry.org/Highlights/2012/16July.shtm
... construction of cyclic quaternary centers. Addition of phenylacetylene to cyclopentanone followed by dehydration and Shi epoxidation gave the epoxide 10. Opening of the epoxide with allylmagnesium chloride proceeded ...
URL: https://www.organic-chemistry.org/Highlights/2005/08August.shtm
... synthesis was carried out in the racemic series, enantiomerically-enriched 9 could be prepared by Shi epoxidation of the ?,?-unsaturated ketone from Birch reduction followed by hydrolysis. ...
URL: https://www.organic-chemistry.org/Highlights/2011/07November.shtm
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