Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives
Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Lagoja, Irene M. [verfasserIn] Schantl, Joachim G. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1996 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Molecules - Springer-Verlag, 1996, 1(1996), 9 vom: Sept., Seite 116-118 |
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| Übergeordnetes Werk: |
volume:1 ; year:1996 ; number:9 ; month:09 ; pages:116-118 |
| Links: |
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| DOI / URN: |
10.1007/s007830050020 |
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| 520 | |a Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. | ||
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10.1007/s007830050020 doi (DE-627)SPR007794002 (SPR)s007830050020-e DE-627 ger DE-627 rakwb eng Lagoja, Irene M. verfasserin aut Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives 1996 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. One-pot-synthesis (dpeaa)DE-He213 N-aminoimidazole-2-thiones (dpeaa)DE-He213 N-aminoimidazoles (dpeaa)DE-He213 Wanzlick-type carbenes (dpeaa)DE-He213 nucleophilic carbenes (dpeaa)DE-He213 Schantl, Joachim G. verfasserin aut Enthalten in Molecules Springer-Verlag, 1996 1(1996), 9 vom: Sept., Seite 116-118 (DE-627)SPR007793685 nnns volume:1 year:1996 number:9 month:09 pages:116-118 https://dx.doi.org/10.1007/s007830050020 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER AR 1 1996 9 09 116-118 |
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10.1007/s007830050020 doi (DE-627)SPR007794002 (SPR)s007830050020-e DE-627 ger DE-627 rakwb eng Lagoja, Irene M. verfasserin aut Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives 1996 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. One-pot-synthesis (dpeaa)DE-He213 N-aminoimidazole-2-thiones (dpeaa)DE-He213 N-aminoimidazoles (dpeaa)DE-He213 Wanzlick-type carbenes (dpeaa)DE-He213 nucleophilic carbenes (dpeaa)DE-He213 Schantl, Joachim G. verfasserin aut Enthalten in Molecules Springer-Verlag, 1996 1(1996), 9 vom: Sept., Seite 116-118 (DE-627)SPR007793685 nnns volume:1 year:1996 number:9 month:09 pages:116-118 https://dx.doi.org/10.1007/s007830050020 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER AR 1 1996 9 09 116-118 |
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10.1007/s007830050020 doi (DE-627)SPR007794002 (SPR)s007830050020-e DE-627 ger DE-627 rakwb eng Lagoja, Irene M. verfasserin aut Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives 1996 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. One-pot-synthesis (dpeaa)DE-He213 N-aminoimidazole-2-thiones (dpeaa)DE-He213 N-aminoimidazoles (dpeaa)DE-He213 Wanzlick-type carbenes (dpeaa)DE-He213 nucleophilic carbenes (dpeaa)DE-He213 Schantl, Joachim G. verfasserin aut Enthalten in Molecules Springer-Verlag, 1996 1(1996), 9 vom: Sept., Seite 116-118 (DE-627)SPR007793685 nnns volume:1 year:1996 number:9 month:09 pages:116-118 https://dx.doi.org/10.1007/s007830050020 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER AR 1 1996 9 09 116-118 |
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10.1007/s007830050020 doi (DE-627)SPR007794002 (SPR)s007830050020-e DE-627 ger DE-627 rakwb eng Lagoja, Irene M. verfasserin aut Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives 1996 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. One-pot-synthesis (dpeaa)DE-He213 N-aminoimidazole-2-thiones (dpeaa)DE-He213 N-aminoimidazoles (dpeaa)DE-He213 Wanzlick-type carbenes (dpeaa)DE-He213 nucleophilic carbenes (dpeaa)DE-He213 Schantl, Joachim G. verfasserin aut Enthalten in Molecules Springer-Verlag, 1996 1(1996), 9 vom: Sept., Seite 116-118 (DE-627)SPR007793685 nnns volume:1 year:1996 number:9 month:09 pages:116-118 https://dx.doi.org/10.1007/s007830050020 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER AR 1 1996 9 09 116-118 |
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10.1007/s007830050020 doi (DE-627)SPR007794002 (SPR)s007830050020-e DE-627 ger DE-627 rakwb eng Lagoja, Irene M. verfasserin aut Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives 1996 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. One-pot-synthesis (dpeaa)DE-He213 N-aminoimidazole-2-thiones (dpeaa)DE-He213 N-aminoimidazoles (dpeaa)DE-He213 Wanzlick-type carbenes (dpeaa)DE-He213 nucleophilic carbenes (dpeaa)DE-He213 Schantl, Joachim G. verfasserin aut Enthalten in Molecules Springer-Verlag, 1996 1(1996), 9 vom: Sept., Seite 116-118 (DE-627)SPR007793685 nnns volume:1 year:1996 number:9 month:09 pages:116-118 https://dx.doi.org/10.1007/s007830050020 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER AR 1 1996 9 09 116-118 |
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Lagoja, Irene M. misc One-pot-synthesis misc N-aminoimidazole-2-thiones misc N-aminoimidazoles misc Wanzlick-type carbenes misc nucleophilic carbenes Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives |
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Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. |
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Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. |
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Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material. |
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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">SPR007794002</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20201124022250.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201005s1996 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s007830050020</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR007794002</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s007830050020-e</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">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Lagoja, Irene M.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Direct Synthetic Approach to N-Aminoimidazole-2 thiones and Imidazole Derivatives</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1996</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">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract In an efficient one-pot/multi-step procedure 1-anilino-2,3-dihydro-1H-imidazole-2-thiones were prepared starting from ±-haloketones. The structure of the imidazole-2-thiones were studied with NMR techniques. Further reactions were performed using the imidazole-2-thiones as starting material.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">One-pot-synthesis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">N-aminoimidazole-2-thiones</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">N-aminoimidazoles</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Wanzlick-type carbenes</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">nucleophilic carbenes</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Schantl, Joachim G.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Molecules</subfield><subfield code="d">Springer-Verlag, 1996</subfield><subfield code="g">1(1996), 9 vom: Sept., Seite 116-118</subfield><subfield code="w">(DE-627)SPR007793685</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:1</subfield><subfield code="g">year:1996</subfield><subfield code="g">number:9</subfield><subfield code="g">month:09</subfield><subfield code="g">pages:116-118</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://dx.doi.org/10.1007/s007830050020</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_SPRINGER</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">1</subfield><subfield code="j">1996</subfield><subfield code="e">9</subfield><subfield code="c">09</subfield><subfield code="h">116-118</subfield></datafield></record></collection>
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