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Synthetic Applications of β-Fluoroalkylated α,β-Unsaturated Carbonyl Compounds
β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient building blocks for the synthesis of complex fluorinated compounds. As the fluorinated moiety generally increases their reactivity, it also brings important modifications which can change the chemical behavior and selectivity....
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Published in: | Chemistry : a European journal 2006-01, Vol.12 (4), p.974-979 |
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container_title | Chemistry : a European journal |
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creator | Billard, Thierry |
description | β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient building blocks for the synthesis of complex fluorinated compounds. As the fluorinated moiety generally increases their reactivity, it also brings important modifications which can change the chemical behavior and selectivity. Their use has been already largely demonstrated. Nevertheless, the synthetic potential has not yet been fully explored and, consequently should play an important role in the design of new sophisticated fluorinated molecules. Nevertheless, it shall be important to develop new synthetic methods to enlarge their availability and their diversity.
Efficient fluorinated building blocks are required for the synthesis of complex fluorinated compounds. β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient units for this purpose. A large diversity of reactions can be envisaged with such molecules. |
doi_str_mv | 10.1002/chem.200500466 |
format | article |
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Efficient fluorinated building blocks are required for the synthesis of complex fluorinated compounds. β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient units for this purpose. A large diversity of reactions can be envisaged with such molecules.</description><subject>carbonyl compounds</subject><subject>cycloaddition</subject><subject>fluorine</subject><subject>Michael addition</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkM1O3DAUhS3UCgbaLUuUVVdkev0_XqKIn0q0VUUrpG4sj-2IgBMHO1Gbx6IPwjM1dEbArqsrHX3n09VB6BDDEgOQj_bGt0sCwAGYEDtogTnBJZWCv0ELUEyWglO1h_ZzvgUAJSjdRXtYgOSMkQX6djV1w40fGluc9H1orBma2OUi1sXjn_IsjDFFE-6mYAbviseH4zn90WUzjOlfUpm0jt0Uiiq2fRw7l9-ht7UJ2b_f3gN0dXb6vbooL7-ef6pOLktLlBCl5EQx7NaYkXp-ETtZr5RSngC1jkJNrQLvOF85jw2xUjpWC6OcwUw5SQ_Qh421T_F-9HnQbZOtD8F0Po5ZSxArLijM4HID2hRzTr7WfWpakyaNQT9NqJ8m1M8TzoWjrXlct9694NvNZkBtgF9N8NN_dLq6OP38Wl5uuk0e_O_nrkl3Wkgqub7-cq45q67pT4k1oX8B4Y-PBA</recordid><startdate>20060123</startdate><enddate>20060123</enddate><creator>Billard, Thierry</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060123</creationdate><title>Synthetic Applications of β-Fluoroalkylated α,β-Unsaturated Carbonyl Compounds</title><author>Billard, Thierry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2966-752941db142f6531d7f8999e203cd30f3c90ed558de1a2c77d4f6a9da149d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>carbonyl compounds</topic><topic>cycloaddition</topic><topic>fluorine</topic><topic>Michael addition</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Billard, Thierry</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Billard, Thierry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic Applications of β-Fluoroalkylated α,β-Unsaturated Carbonyl Compounds</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry - A European Journal</addtitle><date>2006-01-23</date><risdate>2006</risdate><volume>12</volume><issue>4</issue><spage>974</spage><epage>979</epage><pages>974-979</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient building blocks for the synthesis of complex fluorinated compounds. As the fluorinated moiety generally increases their reactivity, it also brings important modifications which can change the chemical behavior and selectivity. Their use has been already largely demonstrated. Nevertheless, the synthetic potential has not yet been fully explored and, consequently should play an important role in the design of new sophisticated fluorinated molecules. Nevertheless, it shall be important to develop new synthetic methods to enlarge their availability and their diversity.
Efficient fluorinated building blocks are required for the synthesis of complex fluorinated compounds. β‐Fluoroalkylated α,β‐unsaturated carbonyl compounds constitute efficient units for this purpose. A large diversity of reactions can be envisaged with such molecules.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>16075442</pmid><doi>10.1002/chem.200500466</doi><tpages>6</tpages></addata></record> |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | carbonyl compounds cycloaddition fluorine Michael addition |
title | Synthetic Applications of β-Fluoroalkylated α,β-Unsaturated Carbonyl Compounds |
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