Asymmetric Epoxidation by Chiral Ketones Derived from Carbocyclic Analogues of Fructose

A number of carbocyclic analogues of the fructose-derived ketone 1 have been prepared and investigated for asymmetric epoxidation. The studies show that the oxygen atom of the pyranose ring of 1 has an impact on the catalyst's activity and selectivity. Conformational, electronic, and steric effects are discussed.

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PID https://www.doi.org/10.1021/jo001343i
PID https://www.doi.org/10.1021/jo001343i.s001
URL https://pubs.acs.org/doi/10.1021/jo001343i
URL http://dx.doi.org/10.1021/jo001343i
URL https://figshare.com/articles/journal_contribution/Asymmetric_Epoxidation_by_Chiral_Ketones_Derived_from_Carbocyclic_Analogues_of_Fructose/3687309
URL https://www.ncbi.nlm.nih.gov/pubmed/11429824
URL https://academic.microsoft.com/#/detail/2009952861
URL https://pubs.acs.org/doi/pdf/10.1021/jo001343i
URL https://pubs.acs.org/doi/abs/10.1021/jo001343i
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Access Right Open Access
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Author Wang, Zhi-Xian
Author Miller, Susie M.
Author Anderson, Oren P.
Author Shi, Yian
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Collected From figshare; Crossref; Microsoft Academic Graph
Hosted By figshare; The Journal of Organic Chemistry
Journal The Journal of Organic Chemistry, 66, null
Publication Date 2016-08-19
Publisher American Chemical Society (ACS)
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Resource Type Other literature type; Article
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::d1a03758866ab2ab76a8f162bce11243
Author jsonws_user
Last Updated 25 December 2020, 02:35 (CET)
Created 25 December 2020, 02:35 (CET)