Nitro and aminobenzimidazoles
A summary of the preparation methods of 2 tautomeric and 4 N -methylated benzimidazoles with a nitro group on the benzene ring ( 1–6 ) and with an amino group in the same positions ( 7–12 ) were summarized. Annular tautomerism of the title compounds 1–12 has been studied using 1 H, 13 C and 15 N NMR...
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| Veröffentlicht in: | Acta Chimica Slovaca 2018-10, Vol.11 (2), p.182-188 |
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| container_title | Acta Chimica Slovaca |
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| creator | Milata, Viktor |
| description | A summary of the preparation methods of 2 tautomeric and 4
N
-methylated benzimidazoles with a nitro group on the benzene ring (
1–6
) and with an amino group in the same positions (
7–12
) were summarized. Annular tautomerism of the title compounds
1–12
has been studied using
1
H,
13
C and
15
N NMR spectra in liquid and solid state (CPMAS), UV spectra and quantum chemical calculations. |
| doi_str_mv | 10.2478/acs-2018-0026 |
| format | Article |
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N
-methylated benzimidazoles with a nitro group on the benzene ring (
1–6
) and with an amino group in the same positions (
7–12
) were summarized. Annular tautomerism of the title compounds
1–12
has been studied using
1
H,
13
C and
15
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N
-methylated benzimidazoles with a nitro group on the benzene ring (
1–6
) and with an amino group in the same positions (
7–12
) were summarized. Annular tautomerism of the title compounds
1–12
has been studied using
1
H,
13
C and
15
N NMR spectra in liquid and solid state (CPMAS), UV spectra and quantum chemical calculations.</description><issn>1337-978X</issn><issn>1337-978X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpNz81KAzEUBeAgCpbapUuhLxC9SW5m0qUU_6DoRsFduLlJINCZkaQb-_R20IWrc1aH8wlxreBWY-_uiJvUoJwE0N2ZWChjernp3ef5v34pVq2VAGiNchZxIW5ey6FOaxrjmoYyTiGNxzKUSMdpn9qVuMi0b2n1l0vx8fjwvn2Wu7enl-39TrK27iCTQlYMyW46YMOYSCPEYIIGxwYwnB5yUlpnjGhBhdxTZMqBuj6mnM1SyN9drlNrNWX_VctA9dsr8DPPn3h-5vmZZ34AakhDWg</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Milata, Viktor</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20181001</creationdate><title>Nitro and aminobenzimidazoles</title><author>Milata, Viktor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c258t-e14c1c0e5960c3c4ea240db3b208c304b247ce122f4d4501bf7adcafba67deff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milata, Viktor</creatorcontrib><collection>CrossRef</collection><jtitle>Acta Chimica Slovaca</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milata, Viktor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitro and aminobenzimidazoles</atitle><jtitle>Acta Chimica Slovaca</jtitle><date>2018-10-01</date><risdate>2018</risdate><volume>11</volume><issue>2</issue><spage>182</spage><epage>188</epage><pages>182-188</pages><issn>1337-978X</issn><eissn>1337-978X</eissn><abstract>A summary of the preparation methods of 2 tautomeric and 4
N
-methylated benzimidazoles with a nitro group on the benzene ring (
1–6
) and with an amino group in the same positions (
7–12
) were summarized. Annular tautomerism of the title compounds
1–12
has been studied using
1
H,
13
C and
15
N NMR spectra in liquid and solid state (CPMAS), UV spectra and quantum chemical calculations.</abstract><doi>10.2478/acs-2018-0026</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1337-978X |
| ispartof | Acta Chimica Slovaca, 2018-10, Vol.11 (2), p.182-188 |
| issn | 1337-978X 1337-978X |
| language | eng |
| recordid | cdi_crossref_primary_10_2478_acs_2018_0026 |
| source | Alma/SFX Local Collection |
| title | Nitro and aminobenzimidazoles |
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