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dc.contributor.authorRiedl, Rainer-
dc.contributor.authorTappe, Robert-
dc.contributor.authorBerkessel, Albrecht-
dc.date.accessioned2018-02-14T07:48:10Z-
dc.date.available2018-02-14T07:48:10Z-
dc.date.issued1998-
dc.identifier.issn0002-7863de_CH
dc.identifier.issn1520-5126de_CH
dc.identifier.urihttps://digitalcollection.zhaw.ch/handle/11475/2757-
dc.description.abstractThe aim of this study was (I) to define the scope and limitations of the Sharpless asymmetric dihydroxylation (AD) for polymer-bound olefins of different structural types and (II) to elaborate HRMAS NMR methods for the direct on-bead monitoring of the asymmetric dihydroxylation, including the on-bead determination of enantiomeric excess (ee). (I) 2-Methoxy-4-(2-propenyl)phenol (eugenol, E), 10-undecenoic acid (U), and (E)-4-hydroxystilbene (S) were bound to Wang-resin or TentaGel S-OH. These olefins gave low (E, 32%), intermediate (U, 88%), and very high enantiomeric excesses (S, >99%) when treated with AD mix β in solution. When bound to the polymers, the trend of the enantioselectivities remained the same [S (97%) > U (20−45%) > E (0−3%)]. However, the absolute ee values demonstrate that only the most selective types of substrates in homogeneous solution have practical potential for enantioselective AD on solid phase. (II) HRMAS NMR was successfully used for on-bead monitoring and for the first time for the ee measurement of the polymer-bound dihydroxylation product. As an example, the full assignment of all resonances of polymer-bound 10-undecenoic acid (U) and its dihydroxylation product is presented. For the ee measurement, the polymer-bound dihydroxylation product was derivatized with Mosher's acid. The integration of seven different pairs of resonances in the 13C HRMAS NMR of the diastereomeric Mosher esters gave (in each case) an ee value that agreed within <1% with that determined by chiral HPLC after cleavage of the AD product.de_CH
dc.language.isoende_CH
dc.publisherAmerican Chemical Societyde_CH
dc.relation.ispartofJournal of the American Chemical Societyde_CH
dc.rightsLicence according to publishing contractde_CH
dc.subjectNMRde_CH
dc.subjectSolid phase synthesisde_CH
dc.subjectOrganic chemistryde_CH
dc.subject.ddc540: Chemiede_CH
dc.titleProbing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excessde_CH
dc.typeBeitrag in wissenschaftlicher Zeitschriftde_CH
dcterms.typeTextde_CH
zhaw.departementLife Sciences und Facility Managementde_CH
zhaw.organisationalunitInstitut für Chemie und Biotechnologie (ICBT)de_CH
dc.identifier.doi10.1021/ja980183dde_CH
zhaw.funding.euNode_CH
zhaw.issue35de_CH
zhaw.originated.zhawYesde_CH
zhaw.pages.end9000de_CH
zhaw.pages.start8994de_CH
zhaw.publication.statuspublishedVersionde_CH
zhaw.volume120de_CH
zhaw.publication.reviewPeer review (Publikation)de_CH
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Riedl, R., Tappe, R., & Berkessel, A. (1998). Probing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excess. Journal of the American Chemical Society, 120(35), 8994–9000. https://doi.org/10.1021/ja980183d
Riedl, R., Tappe, R. and Berkessel, A. (1998) ‘Probing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excess’, Journal of the American Chemical Society, 120(35), pp. 8994–9000. Available at: https://doi.org/10.1021/ja980183d.
R. Riedl, R. Tappe, and A. Berkessel, “Probing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excess,” Journal of the American Chemical Society, vol. 120, no. 35, pp. 8994–9000, 1998, doi: 10.1021/ja980183d.
RIEDL, Rainer, Robert TAPPE und Albrecht BERKESSEL, 1998. Probing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excess. Journal of the American Chemical Society. 1998. Bd. 120, Nr. 35, S. 8994–9000. DOI 10.1021/ja980183d
Riedl, Rainer, Robert Tappe, and Albrecht Berkessel. 1998. “Probing the Scope of the Asymmetric Dihydroxylation of Polymer-Bound Olefins : Monitoring by HRMAS NMR Allows for Reaction Control and On-Bead Measurement of Enantiomeric Excess.” Journal of the American Chemical Society 120 (35): 8994–9000. https://doi.org/10.1021/ja980183d.
Riedl, Rainer, et al. “Probing the Scope of the Asymmetric Dihydroxylation of Polymer-Bound Olefins : Monitoring by HRMAS NMR Allows for Reaction Control and On-Bead Measurement of Enantiomeric Excess.” Journal of the American Chemical Society, vol. 120, no. 35, 1998, pp. 8994–9000, https://doi.org/10.1021/ja980183d.


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