Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides
Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity.
Autor*in: |
Bakbardina, O. V. [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
2006 |
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Schlagwörter: |
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Anmerkung: |
© Pleiades Publishing, Inc. 2006 |
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Übergeordnetes Werk: |
Enthalten in: Russian journal of applied chemistry - Nauka/Interperiodica, 1993, 79(2006), 3 vom: März, Seite 504-505 |
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Übergeordnetes Werk: |
volume:79 ; year:2006 ; number:3 ; month:03 ; pages:504-505 |
Links: |
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DOI / URN: |
10.1134/S1070427206030384 |
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Katalog-ID: |
OLC2063615748 |
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650 | 4 | |a Elemental Sulfur | |
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700 | 1 | |a Fazylov, S. D. |4 aut | |
700 | 1 | |a Baimagambetov, E. Zh. |4 aut | |
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10.1134/S1070427206030384 doi (DE-627)OLC2063615748 (DE-He213)S1070427206030384-p DE-627 ger DE-627 rakwb eng 540 VZ Bakbardina, O. V. verfasserin aut Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides 2006 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Pleiades Publishing, Inc. 2006 Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. Elemental Sulfur Biological Activity Triethylamine Cytisine Anabasine Rakhimzhanova, N. Zh. aut Gazalieva, M. A. aut Fazylov, S. D. aut Baimagambetov, E. Zh. aut Enthalten in Russian journal of applied chemistry Nauka/Interperiodica, 1993 79(2006), 3 vom: März, Seite 504-505 (DE-627)181999927 (DE-600)1181520-6 (DE-576)038881543 1070-4272 nnns volume:79 year:2006 number:3 month:03 pages:504-505 https://doi.org/10.1134/S1070427206030384 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 AR 79 2006 3 03 504-505 |
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10.1134/S1070427206030384 doi (DE-627)OLC2063615748 (DE-He213)S1070427206030384-p DE-627 ger DE-627 rakwb eng 540 VZ Bakbardina, O. V. verfasserin aut Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides 2006 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Pleiades Publishing, Inc. 2006 Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. Elemental Sulfur Biological Activity Triethylamine Cytisine Anabasine Rakhimzhanova, N. Zh. aut Gazalieva, M. A. aut Fazylov, S. D. aut Baimagambetov, E. Zh. aut Enthalten in Russian journal of applied chemistry Nauka/Interperiodica, 1993 79(2006), 3 vom: März, Seite 504-505 (DE-627)181999927 (DE-600)1181520-6 (DE-576)038881543 1070-4272 nnns volume:79 year:2006 number:3 month:03 pages:504-505 https://doi.org/10.1134/S1070427206030384 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 AR 79 2006 3 03 504-505 |
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10.1134/S1070427206030384 doi (DE-627)OLC2063615748 (DE-He213)S1070427206030384-p DE-627 ger DE-627 rakwb eng 540 VZ Bakbardina, O. V. verfasserin aut Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides 2006 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Pleiades Publishing, Inc. 2006 Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. Elemental Sulfur Biological Activity Triethylamine Cytisine Anabasine Rakhimzhanova, N. Zh. aut Gazalieva, M. A. aut Fazylov, S. D. aut Baimagambetov, E. Zh. aut Enthalten in Russian journal of applied chemistry Nauka/Interperiodica, 1993 79(2006), 3 vom: März, Seite 504-505 (DE-627)181999927 (DE-600)1181520-6 (DE-576)038881543 1070-4272 nnns volume:79 year:2006 number:3 month:03 pages:504-505 https://doi.org/10.1134/S1070427206030384 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 AR 79 2006 3 03 504-505 |
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10.1134/S1070427206030384 doi (DE-627)OLC2063615748 (DE-He213)S1070427206030384-p DE-627 ger DE-627 rakwb eng 540 VZ Bakbardina, O. V. verfasserin aut Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides 2006 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Pleiades Publishing, Inc. 2006 Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. Elemental Sulfur Biological Activity Triethylamine Cytisine Anabasine Rakhimzhanova, N. Zh. aut Gazalieva, M. A. aut Fazylov, S. D. aut Baimagambetov, E. Zh. aut Enthalten in Russian journal of applied chemistry Nauka/Interperiodica, 1993 79(2006), 3 vom: März, Seite 504-505 (DE-627)181999927 (DE-600)1181520-6 (DE-576)038881543 1070-4272 nnns volume:79 year:2006 number:3 month:03 pages:504-505 https://doi.org/10.1134/S1070427206030384 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 AR 79 2006 3 03 504-505 |
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10.1134/S1070427206030384 doi (DE-627)OLC2063615748 (DE-He213)S1070427206030384-p DE-627 ger DE-627 rakwb eng 540 VZ Bakbardina, O. V. verfasserin aut Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides 2006 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Pleiades Publishing, Inc. 2006 Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. Elemental Sulfur Biological Activity Triethylamine Cytisine Anabasine Rakhimzhanova, N. Zh. aut Gazalieva, M. A. aut Fazylov, S. D. aut Baimagambetov, E. Zh. aut Enthalten in Russian journal of applied chemistry Nauka/Interperiodica, 1993 79(2006), 3 vom: März, Seite 504-505 (DE-627)181999927 (DE-600)1181520-6 (DE-576)038881543 1070-4272 nnns volume:79 year:2006 number:3 month:03 pages:504-505 https://doi.org/10.1134/S1070427206030384 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 AR 79 2006 3 03 504-505 |
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synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides |
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Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides |
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Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. © Pleiades Publishing, Inc. 2006 |
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Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. © Pleiades Publishing, Inc. 2006 |
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Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity. © Pleiades Publishing, Inc. 2006 |
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Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides |
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V.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2006</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Pleiades Publishing, Inc. 2006</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. 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Zh.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Russian journal of applied chemistry</subfield><subfield code="d">Nauka/Interperiodica, 1993</subfield><subfield code="g">79(2006), 3 vom: März, Seite 504-505</subfield><subfield code="w">(DE-627)181999927</subfield><subfield code="w">(DE-600)1181520-6</subfield><subfield code="w">(DE-576)038881543</subfield><subfield code="x">1070-4272</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:79</subfield><subfield code="g">year:2006</subfield><subfield code="g">number:3</subfield><subfield code="g">month:03</subfield><subfield code="g">pages:504-505</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1134/S1070427206030384</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-DE-84</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">79</subfield><subfield code="j">2006</subfield><subfield code="e">3</subfield><subfield code="c">03</subfield><subfield code="h">504-505</subfield></datafield></record></collection>
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