Synthesis and Structure of Geminally Activated Nitroethenes of the Indole Series
A series of 2-(indol-3-yl)-1-nitroethenes containing an ester, acetyl, benzoyl, or cyano group in the geminal position with respect to the nitro group have been synthesized, and their structure has been studied by 1 H, 13 C−{ 1 H} NMR, IR, and UV spectroscopy.
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| Veröffentlicht in: | Russian journal of general chemistry 2019-05, Vol.89 (5), p.870-880 |
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| container_end_page | 880 |
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| container_issue | 5 |
| container_start_page | 870 |
| container_title | Russian journal of general chemistry |
| container_volume | 89 |
| creator | Baichurin, R. I. Fedorushchenko, A. A. Aboskalova, N. I. Baichurina, L. V. Felgendler, A. V. Makarenko, S. V. |
| description | A series of 2-(indol-3-yl)-1-nitroethenes containing an ester, acetyl, benzoyl, or cyano group in the geminal position with respect to the nitro group have been synthesized, and their structure has been studied by
1
H,
13
C−{
1
H} NMR, IR, and UV spectroscopy. |
| doi_str_mv | 10.1134/S1070363219050037 |
| format | Article |
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H} NMR, IR, and UV spectroscopy.</description><subject>Amino acids</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Cyanides</subject><subject>Cyano groups</subject><subject>Infrared spectroscopy</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Thiophene</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kV1LwzAUhoMoOD9-gHcFrztPmrZpL8fQORgqVK9Dmp7MjK6ZSSbs35sxUUQlFznkPE_ykkPIFYUxpSy_aShwYCXLaA0FAONHZERLqFLGCjiOdWyn-_4pOfN-BUABymxEnprdEF7RG5_IoUua4LYqbB0mViczXJtB9v0umahg3mXALnkwwVmMxoB-z8QqmQ-d7TFp0Bn0F-REy97j5ed-Tl7ubp-n9-nicTafThapYhULac2p7IqiZiqvWi0ZqjKmLgrVAmcIra4kxxzaCqoqK1rGtUIsWdt1vMwkKHZOrg_3bpx926IPYmW3Lsb1IsvyOmo0PvRFLWWPwgzaBifV2nglJjzjOS9oziI1_oOKq4s_oOyA2sTzHwI9CMpZ7x1qsXFmLd1OUBD7eYhf84hOdnB8ZIcluu_A_0sfKCKKYQ</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Baichurin, R. I.</creator><creator>Fedorushchenko, A. A.</creator><creator>Aboskalova, N. I.</creator><creator>Baichurina, L. V.</creator><creator>Felgendler, A. V.</creator><creator>Makarenko, S. V.</creator><general>Pleiades Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20190501</creationdate><title>Synthesis and Structure of Geminally Activated Nitroethenes of the Indole Series</title><author>Baichurin, R. I. ; Fedorushchenko, A. A. ; Aboskalova, N. I. ; Baichurina, L. V. ; Felgendler, A. V. ; Makarenko, S. V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-971ad5593c48bfa3ec600355cb073e0bf8a7e40b808825b37fcee63bdd762a0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amino acids</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Cyanides</topic><topic>Cyano groups</topic><topic>Infrared spectroscopy</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Thiophene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baichurin, R. I.</creatorcontrib><creatorcontrib>Fedorushchenko, A. A.</creatorcontrib><creatorcontrib>Aboskalova, N. I.</creatorcontrib><creatorcontrib>Baichurina, L. V.</creatorcontrib><creatorcontrib>Felgendler, A. V.</creatorcontrib><creatorcontrib>Makarenko, S. V.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baichurin, R. I.</au><au>Fedorushchenko, A. A.</au><au>Aboskalova, N. I.</au><au>Baichurina, L. V.</au><au>Felgendler, A. V.</au><au>Makarenko, S. V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Structure of Geminally Activated Nitroethenes of the Indole Series</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2019-05-01</date><risdate>2019</risdate><volume>89</volume><issue>5</issue><spage>870</spage><epage>880</epage><pages>870-880</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>A series of 2-(indol-3-yl)-1-nitroethenes containing an ester, acetyl, benzoyl, or cyano group in the geminal position with respect to the nitro group have been synthesized, and their structure has been studied by
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| fulltext | fulltext |
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| ispartof | Russian journal of general chemistry, 2019-05, Vol.89 (5), p.870-880 |
| issn | 1070-3632 1608-3350 |
| language | eng |
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| source | SpringerNature Journals |
| subjects | Amino acids Chemistry Chemistry and Materials Science Chemistry/Food Science Cyanides Cyano groups Infrared spectroscopy NMR Nuclear magnetic resonance Thiophene |
| title | Synthesis and Structure of Geminally Activated Nitroethenes of the Indole Series |
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