Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin
Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an i...
Ausführliche Beschreibung
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| Autor*in: |
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| Format: |
E-Artikel |
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| Sprache: |
Deutsch |
| Erschienen: |
1984 |
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| Umfang: |
4 Ill. ; 1 Tab. 9 |
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| Reproduktion: |
Wiley InterScience Backfile Collection 1832-2000 |
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| Übergeordnetes Werk: |
in: Helvetica Chimica Acta - New York, NY : Wiley-VCH, 67(1984) vom: Juli, Seite 1897-1905 |
| Übergeordnetes Werk: |
volume:67 ; year:1984 ; month:07 ; pages:1897-1905 ; extent:9 |
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NLEJ162651856 |
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| 520 | |a Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. | ||
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| 700 | 1 | |a Winkler, Tammo |4 oth | |
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(DE-627)NLEJ162651856 DE-627 ger DE-627 rakwb ger Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin 1984 4 Ill. 1 Tab. 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. Wiley InterScience Backfile Collection 1832-2000 Baumann, Marcus E. oth Bosshard, Hans oth Breitenstein, Werner oth Rihs, Grety oth Winkler, Tammo oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 67(1984) vom: Juli, Seite 1897-1905 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:67 year:1984 month:07 pages:1897-1905 extent:9 http://dx.doi.org/10.1002/hlca.19840670728 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 67 1984 7 1897-1905 9 |
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(DE-627)NLEJ162651856 DE-627 ger DE-627 rakwb ger Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin 1984 4 Ill. 1 Tab. 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. Wiley InterScience Backfile Collection 1832-2000 Baumann, Marcus E. oth Bosshard, Hans oth Breitenstein, Werner oth Rihs, Grety oth Winkler, Tammo oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 67(1984) vom: Juli, Seite 1897-1905 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:67 year:1984 month:07 pages:1897-1905 extent:9 http://dx.doi.org/10.1002/hlca.19840670728 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 67 1984 7 1897-1905 9 |
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(DE-627)NLEJ162651856 DE-627 ger DE-627 rakwb ger Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin 1984 4 Ill. 1 Tab. 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. Wiley InterScience Backfile Collection 1832-2000 Baumann, Marcus E. oth Bosshard, Hans oth Breitenstein, Werner oth Rihs, Grety oth Winkler, Tammo oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 67(1984) vom: Juli, Seite 1897-1905 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:67 year:1984 month:07 pages:1897-1905 extent:9 http://dx.doi.org/10.1002/hlca.19840670728 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 67 1984 7 1897-1905 9 |
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(DE-627)NLEJ162651856 DE-627 ger DE-627 rakwb ger Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin 1984 4 Ill. 1 Tab. 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. Wiley InterScience Backfile Collection 1832-2000 Baumann, Marcus E. oth Bosshard, Hans oth Breitenstein, Werner oth Rihs, Grety oth Winkler, Tammo oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 67(1984) vom: Juli, Seite 1897-1905 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:67 year:1984 month:07 pages:1897-1905 extent:9 http://dx.doi.org/10.1002/hlca.19840670728 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 67 1984 7 1897-1905 9 |
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(DE-627)NLEJ162651856 DE-627 ger DE-627 rakwb ger Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin 1984 4 Ill. 1 Tab. 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. Wiley InterScience Backfile Collection 1832-2000 Baumann, Marcus E. oth Bosshard, Hans oth Breitenstein, Werner oth Rihs, Grety oth Winkler, Tammo oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 67(1984) vom: Juli, Seite 1897-1905 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:67 year:1984 month:07 pages:1897-1905 extent:9 http://dx.doi.org/10.1002/hlca.19840670728 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 67 1984 7 1897-1905 9 |
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Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin |
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Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin |
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mechanismus der decarboxylativen dimerisierung von maleinsäureanhydrid zu dimethylmaleinsäureanhydrid unter einfluss von 2-aminopyridin |
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Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin |
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Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. |
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Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. |
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Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride. |
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Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ162651856</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707094545.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070201s1984 xx |||||o 00| ||ger c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ162651856</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">ger</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Mechanismus der decarboxylativen Dimerisierung von Maleinsäureanhydrid zu Dimethylmaleinsäureanhydrid unter Einfluss von 2-Aminopyridin</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1984</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="b">4 Ill.</subfield><subfield code="b">1 Tab.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">9</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Mechanism of the Decarboxylative Dimerization of Maleic Anhydride to Dimethylmaleic Anhydride under the Influence of 2-AminopyridineThe mechanism of the decarboxylative dimerization of maleic anhydride to dimethylmaleic anhydride was investigated. It was shwon that imidazo[1,2-a] pyridines play an important role as intermediates in this rather unusual transformation, the key step being a Michael addition of 5 to maleic anhydride.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Wiley InterScience Backfile Collection 1832-2000</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Baumann, Marcus E.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bosshard, Hans</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Breitenstein, Werner</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Rihs, Grety</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Winkler, Tammo</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Helvetica Chimica Acta</subfield><subfield code="d">New York, NY : Wiley-VCH</subfield><subfield code="g">67(1984) vom: Juli, Seite 1897-1905</subfield><subfield code="w">(DE-627)NLEJ159071178</subfield><subfield code="w">(DE-600)1475013-2</subfield><subfield code="x">0018-019X</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:67</subfield><subfield code="g">year:1984</subfield><subfield code="g">month:07</subfield><subfield code="g">pages:1897-1905</subfield><subfield code="g">extent:9</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1002/hlca.19840670728</subfield><subfield code="q">text/html</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-WIS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">67</subfield><subfield code="j">1984</subfield><subfield code="c">7</subfield><subfield code="h">1897-1905</subfield><subfield code="g">9</subfield></datafield></record></collection>
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