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Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals
The single coordination-site transition metal Lewis acids [CpM(BIPHOP-F)][SbF6] (M = Fe, Ru) catalyze the [3+2] dipolar cycloaddition reaction between reactive nitrones and α,β-unsaturated aldehydes to give chiral isoxazolidines with ee values of 75 to >96%. The stereochemistry of the major enant...
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Published in: | Journal of the American Chemical Society 2002-05, Vol.124 (18), p.4968-4969 |
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container_end_page | 4969 |
container_issue | 18 |
container_start_page | 4968 |
container_title | Journal of the American Chemical Society |
container_volume | 124 |
creator | Viton, Florian Bernardinelli, Gérald Kündig, E. Peter |
description | The single coordination-site transition metal Lewis acids [CpM(BIPHOP-F)][SbF6] (M = Fe, Ru) catalyze the [3+2] dipolar cycloaddition reaction between reactive nitrones and α,β-unsaturated aldehydes to give chiral isoxazolidines with ee values of 75 to >96%. The stereochemistry of the major enantiomer is consistent with an endo approach of the nitrone to the Cα-Si-face of the enal in the s-trans conformation in the (R,R)-catalyst site. The absolute configuration is based on an X-ray structure determination. |
doi_str_mv | 10.1021/ja017814f |
format | article |
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The absolute configuration is based on an X-ray structure determination.</description><subject>Acrolein - analogs & derivatives</subject><subject>Acrolein - chemistry</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Iron - chemistry</subject><subject>Isoxazoles - chemical synthesis</subject><subject>Models, Molecular</subject><subject>Nitrogen Oxides - chemistry</subject><subject>Organic chemistry</subject><subject>Organometallic Compounds - chemistry</subject><subject>Ruthenium - chemistry</subject><subject>Stereoisomerism</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpt0M1uEzEUBWALgWgoLHgB5A2VkBjwHY_HzjJKW6gUAUqLxM6647kjHOYntWdUwtPjkKjZsLItfzrXPoy9BvEBRA4fNyhAGyiaJ2wGKheZgrx8ymZCiDzTppRn7EWMm3QscgPP2RnA3ORSqRm7vwlDz7Gv-Xoaf1Lvp46v6MFHvnC-5kscsd39oZov4q7raAzecXgvs0u_HVoMfLlz7YB17UefctaEbr-JvKLxgajnX_yYBlD8N-Kqxza-ZM-atNCr43rOvl9f3S0_Z6uvn26Wi1WGRaHGrKqBClFXJAvjcqMkSHK6nBeuQYHOKEWmIgQwc6d0k9cACVeVkVqV0jTynF0ccrdhuJ8ojrbz0VHbYk_DFK2GxLQSCb47QBeGGAM1dht8h2FnQdh9v_ax32TfHEOnqqP6JI-FJvD2CDA6bJuAvfPx5GSpCplDctnB-TjS78d7DL9sqdMX7N23W3urr3_osri061Muumg3wxT2Vf7ngX8BxJWd_A</recordid><startdate>20020508</startdate><enddate>20020508</enddate><creator>Viton, Florian</creator><creator>Bernardinelli, Gérald</creator><creator>Kündig, E. 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Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a445t-bd1e40dbe348c285313ec7694cfa0ac855e8bea1189c57f2d11dbebb8375638f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acrolein - analogs & derivatives</topic><topic>Acrolein - chemistry</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Iron - chemistry</topic><topic>Isoxazoles - chemical synthesis</topic><topic>Models, Molecular</topic><topic>Nitrogen Oxides - chemistry</topic><topic>Organic chemistry</topic><topic>Organometallic Compounds - chemistry</topic><topic>Ruthenium - chemistry</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Viton, Florian</creatorcontrib><creatorcontrib>Bernardinelli, Gérald</creatorcontrib><creatorcontrib>Kündig, E. Peter</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Viton, Florian</au><au>Bernardinelli, Gérald</au><au>Kündig, E. Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2002-05-08</date><risdate>2002</risdate><volume>124</volume><issue>18</issue><spage>4968</spage><epage>4969</epage><pages>4968-4969</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><coden>JACSAT</coden><abstract>The single coordination-site transition metal Lewis acids [CpM(BIPHOP-F)][SbF6] (M = Fe, Ru) catalyze the [3+2] dipolar cycloaddition reaction between reactive nitrones and α,β-unsaturated aldehydes to give chiral isoxazolidines with ee values of 75 to >96%. The stereochemistry of the major enantiomer is consistent with an endo approach of the nitrone to the Cα-Si-face of the enal in the s-trans conformation in the (R,R)-catalyst site. The absolute configuration is based on an X-ray structure determination.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>11982355</pmid><doi>10.1021/ja017814f</doi><tpages>2</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Acrolein - analogs & derivatives Acrolein - chemistry Catalysis Chemistry Exact sciences and technology Iron - chemistry Isoxazoles - chemical synthesis Models, Molecular Nitrogen Oxides - chemistry Organic chemistry Organometallic Compounds - chemistry Ruthenium - chemistry Stereoisomerism |
title | Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals |
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