Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes
Condensation of 2-propanoyl-, 2-butanoyl-, and 2-pentanoylcyclohexane-1,3-diones with aromatic aldehydes in the presence of secondary amines (diethylamine, pyrrolidine, morpholine, piperidine, and hexamethyleneimine) leads to the formation of the corresponding 2-[1-(dialkylamino)-2-alkyl-3-aryl-2-pr...
Gespeichert in:
Veröffentlicht in: | Russian journal of general chemistry 2012, Vol.82 (1), p.122-130 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 130 |
---|---|
container_issue | 1 |
container_start_page | 122 |
container_title | Russian journal of general chemistry |
container_volume | 82 |
creator | Rubinov, D. B. Zheldakova, T. A. Zheldakova, R. A. Rubinova, I. L. Baranovski, A. V. Lakhvich, F. A. |
description | Condensation of 2-propanoyl-, 2-butanoyl-, and 2-pentanoylcyclohexane-1,3-diones with aromatic aldehydes in the presence of secondary amines (diethylamine, pyrrolidine, morpholine, piperidine, and hexamethyleneimine) leads to the formation of the corresponding 2-[1-(dialkylamino)-2-alkyl-3-aryl-2-propylidene]cyclohexane-1,3-diones and derivatives of 4
H
-chromen-4,5(6
H
)-dione. A primary screening of some of the resulting enamino derivatives for fungicidal activity has been performed. |
doi_str_mv | 10.1134/S1070363212010203 |
format | Article |
fullrecord | <record><control><sourceid>crossref_sprin</sourceid><recordid>TN_cdi_crossref_primary_10_1134_S1070363212010203</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1134_S1070363212010203</sourcerecordid><originalsourceid>FETCH-LOGICAL-c240t-e2c6cb61a2cc1c6fadb8ff88295181f08b0f2067321da16439e68f4a912a8ea03</originalsourceid><addsrcrecordid>eNp9kM1OwzAQhC0EEqXwANzyABh27dR1jqhAQarEAThHG_-QVGmM7CDI2-Oq3JA47UrzzWpnGLtEuEaU5c0LwhKkkgIFIAiQR2yGCjSXcgHHec8y3-un7CylLWQIlJixu1UYrBsSjV0YiuALwclMvZlMH1r3TYPjeCW5zapLxVc3tgXFsMu4Kai3rp2sS-fsxFOf3MXvnLO3h_vX1SPfPK-fVrcbbkQJI3fCKNMoJGEMGuXJNtp7rUW1QI0edANegFrmEJZQlbJySvuSKhSkHYGcMzzcNTGkFJ2vP2K3ozjVCPW-hvpPDdkjDp6U2eHdxXobPuOQ3_zH9AOJaV4s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes</title><source>Springer Nature - Complete Springer Journals</source><creator>Rubinov, D. B. ; Zheldakova, T. A. ; Zheldakova, R. A. ; Rubinova, I. L. ; Baranovski, A. V. ; Lakhvich, F. A.</creator><creatorcontrib>Rubinov, D. B. ; Zheldakova, T. A. ; Zheldakova, R. A. ; Rubinova, I. L. ; Baranovski, A. V. ; Lakhvich, F. A.</creatorcontrib><description>Condensation of 2-propanoyl-, 2-butanoyl-, and 2-pentanoylcyclohexane-1,3-diones with aromatic aldehydes in the presence of secondary amines (diethylamine, pyrrolidine, morpholine, piperidine, and hexamethyleneimine) leads to the formation of the corresponding 2-[1-(dialkylamino)-2-alkyl-3-aryl-2-propylidene]cyclohexane-1,3-diones and derivatives of 4
H
-chromen-4,5(6
H
)-dione. A primary screening of some of the resulting enamino derivatives for fungicidal activity has been performed.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363212010203</identifier><language>eng</language><publisher>Dordrecht: SP MAIK Nauka/Interperiodica</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science</subject><ispartof>Russian journal of general chemistry, 2012, Vol.82 (1), p.122-130</ispartof><rights>Pleiades Publishing, Ltd. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c240t-e2c6cb61a2cc1c6fadb8ff88295181f08b0f2067321da16439e68f4a912a8ea03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363212010203$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363212010203$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Rubinov, D. B.</creatorcontrib><creatorcontrib>Zheldakova, T. A.</creatorcontrib><creatorcontrib>Zheldakova, R. A.</creatorcontrib><creatorcontrib>Rubinova, I. L.</creatorcontrib><creatorcontrib>Baranovski, A. V.</creatorcontrib><creatorcontrib>Lakhvich, F. A.</creatorcontrib><title>Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>Condensation of 2-propanoyl-, 2-butanoyl-, and 2-pentanoylcyclohexane-1,3-diones with aromatic aldehydes in the presence of secondary amines (diethylamine, pyrrolidine, morpholine, piperidine, and hexamethyleneimine) leads to the formation of the corresponding 2-[1-(dialkylamino)-2-alkyl-3-aryl-2-propylidene]cyclohexane-1,3-diones and derivatives of 4
H
-chromen-4,5(6
H
)-dione. A primary screening of some of the resulting enamino derivatives for fungicidal activity has been performed.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OwzAQhC0EEqXwANzyABh27dR1jqhAQarEAThHG_-QVGmM7CDI2-Oq3JA47UrzzWpnGLtEuEaU5c0LwhKkkgIFIAiQR2yGCjSXcgHHec8y3-un7CylLWQIlJixu1UYrBsSjV0YiuALwclMvZlMH1r3TYPjeCW5zapLxVc3tgXFsMu4Kai3rp2sS-fsxFOf3MXvnLO3h_vX1SPfPK-fVrcbbkQJI3fCKNMoJGEMGuXJNtp7rUW1QI0edANegFrmEJZQlbJySvuSKhSkHYGcMzzcNTGkFJ2vP2K3ozjVCPW-hvpPDdkjDp6U2eHdxXobPuOQ3_zH9AOJaV4s</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Rubinov, D. B.</creator><creator>Zheldakova, T. A.</creator><creator>Zheldakova, R. A.</creator><creator>Rubinova, I. L.</creator><creator>Baranovski, A. V.</creator><creator>Lakhvich, F. A.</creator><general>SP MAIK Nauka/Interperiodica</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2012</creationdate><title>Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes</title><author>Rubinov, D. B. ; Zheldakova, T. A. ; Zheldakova, R. A. ; Rubinova, I. L. ; Baranovski, A. V. ; Lakhvich, F. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c240t-e2c6cb61a2cc1c6fadb8ff88295181f08b0f2067321da16439e68f4a912a8ea03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rubinov, D. B.</creatorcontrib><creatorcontrib>Zheldakova, T. A.</creatorcontrib><creatorcontrib>Zheldakova, R. A.</creatorcontrib><creatorcontrib>Rubinova, I. L.</creatorcontrib><creatorcontrib>Baranovski, A. V.</creatorcontrib><creatorcontrib>Lakhvich, F. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rubinov, D. B.</au><au>Zheldakova, T. A.</au><au>Zheldakova, R. A.</au><au>Rubinova, I. L.</au><au>Baranovski, A. V.</au><au>Lakhvich, F. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2012</date><risdate>2012</risdate><volume>82</volume><issue>1</issue><spage>122</spage><epage>130</epage><pages>122-130</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>Condensation of 2-propanoyl-, 2-butanoyl-, and 2-pentanoylcyclohexane-1,3-diones with aromatic aldehydes in the presence of secondary amines (diethylamine, pyrrolidine, morpholine, piperidine, and hexamethyleneimine) leads to the formation of the corresponding 2-[1-(dialkylamino)-2-alkyl-3-aryl-2-propylidene]cyclohexane-1,3-diones and derivatives of 4
H
-chromen-4,5(6
H
)-dione. A primary screening of some of the resulting enamino derivatives for fungicidal activity has been performed.</abstract><cop>Dordrecht</cop><pub>SP MAIK Nauka/Interperiodica</pub><doi>10.1134/S1070363212010203</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1070-3632 |
ispartof | Russian journal of general chemistry, 2012, Vol.82 (1), p.122-130 |
issn | 1070-3632 1608-3350 |
language | eng |
recordid | cdi_crossref_primary_10_1134_S1070363212010203 |
source | Springer Nature - Complete Springer Journals |
subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science |
title | Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T02%3A33%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_sprin&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Condensation%20of%202-acylcyclohexane-1,3-diones%20with%20aromatic%20aldehydes&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Rubinov,%20D.%20B.&rft.date=2012&rft.volume=82&rft.issue=1&rft.spage=122&rft.epage=130&rft.pages=122-130&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363212010203&rft_dat=%3Ccrossref_sprin%3E10_1134_S1070363212010203%3C/crossref_sprin%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |