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Stereodivergent Synthesis of Enantioenriched 4-Hydroxy-2- cyclopentenones
| dc.contributor.author | Singh, Gurpreet | |
| dc.contributor.author | Meyer, Angelica Michelle | |
| dc.contributor.author | Aubé, Jeffrey | |
| dc.date.accessioned | 2017-04-13T15:20:16Z | |
| dc.date.available | 2017-04-13T15:20:16Z | |
| dc.date.issued | 2014-01-03 | |
| dc.identifier.citation | Singh, G., Meyer, A., & Aubé, J. (2014). Stereodivergent Synthesis of Enantioenriched 4-Hydroxy-2-cyclopentenones. The Journal of Organic Chemistry, 79(1), 452–458. http://doi.org/10.1021/jo402539p | en_US |
| dc.identifier.uri | http://hdl.handle.net/1808/23677 | |
| dc.description.abstract | Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the product), ring-closing metathesis, and simple functional group conversions to provide a set of substituted 4-HCPs in either enantiomeric form. | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo402539p. | en_US |
| dc.title | Stereodivergent Synthesis of Enantioenriched 4-Hydroxy-2- cyclopentenones | en_US |
| dc.type | Article | en_US |
| kusw.kuauthor | Singh, Gurpreet | |
| kusw.kuauthor | Meyer, Angelica | |
| kusw.kuauthor | Aubé, Jeffrey | |
| kusw.kudepartment | Medicinal Chemistry | en_US |
| dc.identifier.doi | 10.1021/jo402539p | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0003-1049-5767 | |
| kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
| kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
| dc.rights.accessrights | openAccess |
