Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives
[Display omitted] Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives to produce the corresponding optically active amine has been performed in the presence of rhodium and iridium catalysts. The optimization of neutral rhodium based catalytic systems by varying the operating...
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Veröffentlicht in: | Tetrahedron: asymmetry 2016-04, Vol.27 (6), p.268-273 |
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container_title | Tetrahedron: asymmetry |
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creator | Maj, Anna M. Suisse, Isabelle Agbossou-Niedercorn, Francine |
description | [Display omitted]
Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives to produce the corresponding optically active amine has been performed in the presence of rhodium and iridium catalysts. The optimization of neutral rhodium based catalytic systems by varying the operating conditions and the ligand around the metallic centre led to high conversions with moderate enantiomeric excesses. |
doi_str_mv | 10.1016/j.tetasy.2016.02.005 |
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Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives to produce the corresponding optically active amine has been performed in the presence of rhodium and iridium catalysts. The optimization of neutral rhodium based catalytic systems by varying the operating conditions and the ligand around the metallic centre led to high conversions with moderate enantiomeric excesses.</description><identifier>ISSN: 0957-4166</identifier><identifier>EISSN: 1362-511X</identifier><identifier>EISSN: 0957-4166</identifier><identifier>DOI: 10.1016/j.tetasy.2016.02.005</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Chemical Sciences</subject><ispartof>Tetrahedron: asymmetry, 2016-04, Vol.27 (6), p.268-273</ispartof><rights>2016 Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-1c8c528a6def4baab0c1041c5dc36ada35d88855014eac977524d52ceaa652eb3</citedby><cites>FETCH-LOGICAL-c340t-1c8c528a6def4baab0c1041c5dc36ada35d88855014eac977524d52ceaa652eb3</cites><orcidid>0000-0002-8453-0492</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tetasy.2016.02.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://hal.science/hal-01715067$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Maj, Anna M.</creatorcontrib><creatorcontrib>Suisse, Isabelle</creatorcontrib><creatorcontrib>Agbossou-Niedercorn, Francine</creatorcontrib><title>Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives</title><title>Tetrahedron: asymmetry</title><description>[Display omitted]
Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives to produce the corresponding optically active amine has been performed in the presence of rhodium and iridium catalysts. The optimization of neutral rhodium based catalytic systems by varying the operating conditions and the ligand around the metallic centre led to high conversions with moderate enantiomeric excesses.</description><subject>Chemical Sciences</subject><issn>0957-4166</issn><issn>1362-511X</issn><issn>0957-4166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kMFKxDAQhoMouK6-gYdeBVMzaZN2L8KyqCsUvCh4C2kydbNsG0lKsW9v14pHT8MM__fDfIRcA0uBgbzbpz32Oo4pn7aU8ZQxcUIWkElOBcD7KVmwlShoDlKek4sY92wKChALUq3j2LbYB2eS3WiD_8BO9853iW8SfptR637OFLbUdRY7CtR3mPgv12KiO5tYDG6YkAHjJTlr9CHi1e9ckrfHh9fNllYvT8-bdUVNlrOegimN4KWWFpu81rpmBlgORliTSW11JmxZlkIwyFGbVVEInlvBDWotBcc6W5KbuXenD-ozuFaHUXnt1HZdqeONQQGCyWKAKZvPWRN8jAGbPwCYOtpTezXbU0d7inE12Zuw-xnD6Y_BYVDROOwMWhfQ9Mp693_BN3DWehw</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Maj, Anna M.</creator><creator>Suisse, Isabelle</creator><creator>Agbossou-Niedercorn, Francine</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-8453-0492</orcidid></search><sort><creationdate>20160401</creationdate><title>Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives</title><author>Maj, Anna M. ; Suisse, Isabelle ; Agbossou-Niedercorn, Francine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-1c8c528a6def4baab0c1041c5dc36ada35d88855014eac977524d52ceaa652eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chemical Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maj, Anna M.</creatorcontrib><creatorcontrib>Suisse, Isabelle</creatorcontrib><creatorcontrib>Agbossou-Niedercorn, Francine</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Tetrahedron: asymmetry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maj, Anna M.</au><au>Suisse, Isabelle</au><au>Agbossou-Niedercorn, Francine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives</atitle><jtitle>Tetrahedron: asymmetry</jtitle><date>2016-04-01</date><risdate>2016</risdate><volume>27</volume><issue>6</issue><spage>268</spage><epage>273</epage><pages>268-273</pages><issn>0957-4166</issn><eissn>1362-511X</eissn><eissn>0957-4166</eissn><abstract>[Display omitted]
Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives to produce the corresponding optically active amine has been performed in the presence of rhodium and iridium catalysts. The optimization of neutral rhodium based catalytic systems by varying the operating conditions and the ligand around the metallic centre led to high conversions with moderate enantiomeric excesses.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tetasy.2016.02.005</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8453-0492</orcidid></addata></record> |
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title | Asymmetric hydrogenation of 2,3-dihydro-1H-inden-1-one oxime and derivatives |
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