A general strategy for construction of a difluoromethyl compound library and its application in synthesis of pseudopeptides bearing a terminal difluoromethyl groupElectronic supplementary information (ESI) available: NMR and high resolution mass spectra. See DOI: 10.1039/c000835d
We describe the development of a novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group. The core of this approach is the conscious design and synthesis of new difluorinated buil...
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creator | Wu, Jingjing Cao, Song Liu, Nianjin Shen, Li Yu, Jinlong Zhang, Jian Li, Hui Qian, Xuhong |
description | We describe the development of a novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group. The core of this approach is the conscious design and synthesis of new difluorinated building blocks which contain inactive and reactive groups on each side of the CF
2
group. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.
A novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group was described. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction. |
doi_str_mv | 10.1039/c000835d |
format | Article |
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2
group. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.
A novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group was described. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c000835d</identifier><language>eng</language><creationdate>2010-05</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Wu, Jingjing</creatorcontrib><creatorcontrib>Cao, Song</creatorcontrib><creatorcontrib>Liu, Nianjin</creatorcontrib><creatorcontrib>Shen, Li</creatorcontrib><creatorcontrib>Yu, Jinlong</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Qian, Xuhong</creatorcontrib><title>A general strategy for construction of a difluoromethyl compound library and its application in synthesis of pseudopeptides bearing a terminal difluoromethyl groupElectronic supplementary information (ESI) available: NMR and high resolution mass spectra. See DOI: 10.1039/c000835d</title><description>We describe the development of a novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group. The core of this approach is the conscious design and synthesis of new difluorinated building blocks which contain inactive and reactive groups on each side of the CF
2
group. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.
A novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group was described. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUE1Lw0AQjaJg_QCPggfnqIfWjWmt7U20Yg8qWO9lm0ySkf1iZyPk37upH4eCeJo3vDfvPSZJjlMxSEU2ucyFEDfZqNhOeulwPO6LUTbZ-cVXYi_ZZ34XIp2Mr4e9rZNbqNCglwo4eBmwaqG0HnJr4t7kgawBW4KEgkrVWG81hrpVUaCdbUwBilZe-hZkxBQYpHOKcrk-JAPcmlAjE3cujrEprEMXqECGFUpPpormAb0mE0tspFTeNm6mMA_eGsqBm-iOGk3oIsnEqvor6ny2mF-A_JCk5ErhFJ6fXtedaqpq8MhWNWuhlszArrOUA1ggwv3LfAqb_ztMdkupGI--50Fy-jB7u3vse86XzpOOBZY_4uw_9uxvdumKMvsEn-6Q6w</recordid><startdate>20100506</startdate><enddate>20100506</enddate><creator>Wu, Jingjing</creator><creator>Cao, Song</creator><creator>Liu, Nianjin</creator><creator>Shen, Li</creator><creator>Yu, Jinlong</creator><creator>Zhang, Jian</creator><creator>Li, Hui</creator><creator>Qian, Xuhong</creator><scope/></search><sort><creationdate>20100506</creationdate><title>A general strategy for construction of a difluoromethyl compound library and its application in synthesis of pseudopeptides bearing a terminal difluoromethyl groupElectronic supplementary information (ESI) available: NMR and high resolution mass spectra. See DOI: 10.1039/c000835d</title><author>Wu, Jingjing ; Cao, Song ; Liu, Nianjin ; Shen, Li ; Yu, Jinlong ; Zhang, Jian ; Li, Hui ; Qian, Xuhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c000835d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Jingjing</creatorcontrib><creatorcontrib>Cao, Song</creatorcontrib><creatorcontrib>Liu, Nianjin</creatorcontrib><creatorcontrib>Shen, Li</creatorcontrib><creatorcontrib>Yu, Jinlong</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Qian, Xuhong</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Jingjing</au><au>Cao, Song</au><au>Liu, Nianjin</au><au>Shen, Li</au><au>Yu, Jinlong</au><au>Zhang, Jian</au><au>Li, Hui</au><au>Qian, Xuhong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A general strategy for construction of a difluoromethyl compound library and its application in synthesis of pseudopeptides bearing a terminal difluoromethyl groupElectronic supplementary information (ESI) available: NMR and high resolution mass spectra. See DOI: 10.1039/c000835d</atitle><date>2010-05-06</date><risdate>2010</risdate><volume>8</volume><issue>1</issue><spage>2386</spage><epage>2391</epage><pages>2386-2391</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>We describe the development of a novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group. The core of this approach is the conscious design and synthesis of new difluorinated building blocks which contain inactive and reactive groups on each side of the CF
2
group. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.
A novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group was described. The strategy is illustrated by application to the synthesis of CF
2
H-bearing pseudopeptides
via
Ugi reaction.</abstract><doi>10.1039/c000835d</doi><tpages>6</tpages></addata></record> |
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title | A general strategy for construction of a difluoromethyl compound library and its application in synthesis of pseudopeptides bearing a terminal difluoromethyl groupElectronic supplementary information (ESI) available: NMR and high resolution mass spectra. See DOI: 10.1039/c000835d |
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