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Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives
Aldol addition of acyclic and cyclic ketones to 4,4,6-trimethyl-4 H -pyrrolo[3,2,1- ij ]quinoline-1,2-diones afforded the corresponding 1-substituted 1-hydroxy-4,4,6-trimethyl-4 H -pyrrolo[3,2,1- ij ]quinolin-2(1 H )-ones. The short-time reduction of 4,4,6-trimethyl-4 H -pyrrolo[3,2,1- ij ]quinoline...
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Published in: | Russian journal of organic chemistry 2021-10, Vol.57 (10), p.1592-1599 |
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container_end_page | 1599 |
container_issue | 10 |
container_start_page | 1592 |
container_title | Russian journal of organic chemistry |
container_volume | 57 |
creator | Novichikhina, N. P. Shestakov, A. S. Skoptsova, A. A. Ashrafova, Z. E. Stolpovskaya, N. V. Kosheleva, E. A. Shatalov, G. V. Ledenyova, I. V. Shikhaliev, Kh. S. |
description | Aldol addition of acyclic and cyclic ketones to 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones afforded the corresponding 1-substituted 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones. The short-time reduction of 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones with sodium tetrahydridoborate gave 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones. |
doi_str_mv | 10.1134/S1070428021100043 |
format | article |
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H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones afforded the corresponding 1-substituted 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones. The short-time reduction of 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones with sodium tetrahydridoborate gave 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S1070428021100043</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Aldehydes ; Chemistry ; Chemistry and Materials Science ; Diketones ; Ketones ; Organic Chemistry ; Quinoline</subject><ispartof>Russian journal of organic chemistry, 2021-10, Vol.57 (10), p.1592-1599</ispartof><rights>Pleiades Publishing, Ltd. 2021</rights><rights>Pleiades Publishing, Ltd. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-2d8f7a6364d15eb080bf9db3ce5953b30f5eaa8f30ef49ff1f6a0592615edf323</citedby><cites>FETCH-LOGICAL-c316t-2d8f7a6364d15eb080bf9db3ce5953b30f5eaa8f30ef49ff1f6a0592615edf323</cites><orcidid>0000-0001-7785-3595 ; 0000-0002-4277-5838 ; 0000-0002-0426-4789 ; 0000-0002-9859-6476 ; 0000-0002-6576-0305 ; 0000-0002-1819-6414 ; 0000-0001-8167-6093 ; 0000-0001-8161-3586 ; 0000-0002-1865-4032</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids></links><search><creatorcontrib>Novichikhina, N. P.</creatorcontrib><creatorcontrib>Shestakov, A. S.</creatorcontrib><creatorcontrib>Skoptsova, A. A.</creatorcontrib><creatorcontrib>Ashrafova, Z. E.</creatorcontrib><creatorcontrib>Stolpovskaya, N. V.</creatorcontrib><creatorcontrib>Kosheleva, E. A.</creatorcontrib><creatorcontrib>Shatalov, G. V.</creatorcontrib><creatorcontrib>Ledenyova, I. V.</creatorcontrib><creatorcontrib>Shikhaliev, Kh. S.</creatorcontrib><title>Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives</title><title>Russian journal of organic chemistry</title><addtitle>Russ J Org Chem</addtitle><description>Aldol addition of acyclic and cyclic ketones to 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones afforded the corresponding 1-substituted 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones. The short-time reduction of 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones with sodium tetrahydridoborate gave 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones.</description><subject>Aldehydes</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Diketones</subject><subject>Ketones</subject><subject>Organic Chemistry</subject><subject>Quinoline</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE9Lw0AQxRdRsFY_gLeAF4Wuzuxs0uQo9U-EqofqSSQkza5uqdl2N63m27ulggfxNA_e772Bx9gxwjkiyYsJwhCkSEEgAoCkHdbDBFJOlNFu0MHmG3-fHXg_2yAoqcfuJ13TvitvfGR19KA-I-R5Vzv71XGZ80XnnJ3bFxqIAXIze12uTGPnpuHiFPMzbhsVXSln1mVr1sofsj1dzr06-rl99nxz_TTK-fjx9m50OeZTwqTlok71sEwokTXGqoIUKp3VFU1VnMVUEehYlWWqCZSWmdaokxLiTCSBrjUJ6rOTbe_C2eVK-baY2ZVrwstCJDAkkcZZGijcUlNnvXdKFwtnPkrXFQjFZrXiz2ohI7YZH9jmTbnf5v9D3-aXbBA</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Novichikhina, N. P.</creator><creator>Shestakov, A. S.</creator><creator>Skoptsova, A. A.</creator><creator>Ashrafova, Z. E.</creator><creator>Stolpovskaya, N. V.</creator><creator>Kosheleva, E. A.</creator><creator>Shatalov, G. V.</creator><creator>Ledenyova, I. V.</creator><creator>Shikhaliev, Kh. S.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-7785-3595</orcidid><orcidid>https://orcid.org/0000-0002-4277-5838</orcidid><orcidid>https://orcid.org/0000-0002-0426-4789</orcidid><orcidid>https://orcid.org/0000-0002-9859-6476</orcidid><orcidid>https://orcid.org/0000-0002-6576-0305</orcidid><orcidid>https://orcid.org/0000-0002-1819-6414</orcidid><orcidid>https://orcid.org/0000-0001-8167-6093</orcidid><orcidid>https://orcid.org/0000-0001-8161-3586</orcidid><orcidid>https://orcid.org/0000-0002-1865-4032</orcidid></search><sort><creationdate>20211001</creationdate><title>Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives</title><author>Novichikhina, N. P. ; Shestakov, A. S. ; Skoptsova, A. A. ; Ashrafova, Z. E. ; Stolpovskaya, N. V. ; Kosheleva, E. A. ; Shatalov, G. V. ; Ledenyova, I. V. ; Shikhaliev, Kh. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-2d8f7a6364d15eb080bf9db3ce5953b30f5eaa8f30ef49ff1f6a0592615edf323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aldehydes</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Diketones</topic><topic>Ketones</topic><topic>Organic Chemistry</topic><topic>Quinoline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Novichikhina, N. P.</creatorcontrib><creatorcontrib>Shestakov, A. S.</creatorcontrib><creatorcontrib>Skoptsova, A. A.</creatorcontrib><creatorcontrib>Ashrafova, Z. E.</creatorcontrib><creatorcontrib>Stolpovskaya, N. V.</creatorcontrib><creatorcontrib>Kosheleva, E. A.</creatorcontrib><creatorcontrib>Shatalov, G. V.</creatorcontrib><creatorcontrib>Ledenyova, I. V.</creatorcontrib><creatorcontrib>Shikhaliev, Kh. S.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Novichikhina, N. P.</au><au>Shestakov, A. S.</au><au>Skoptsova, A. A.</au><au>Ashrafova, Z. E.</au><au>Stolpovskaya, N. V.</au><au>Kosheleva, E. A.</au><au>Shatalov, G. V.</au><au>Ledenyova, I. V.</au><au>Shikhaliev, Kh. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives</atitle><jtitle>Russian journal of organic chemistry</jtitle><stitle>Russ J Org Chem</stitle><date>2021-10-01</date><risdate>2021</risdate><volume>57</volume><issue>10</issue><spage>1592</spage><epage>1599</epage><pages>1592-1599</pages><issn>1070-4280</issn><eissn>1608-3393</eissn><abstract>Aldol addition of acyclic and cyclic ketones to 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones afforded the corresponding 1-substituted 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones. The short-time reduction of 4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinoline-1,2-diones with sodium tetrahydridoborate gave 1-hydroxy-4,4,6-trimethyl-4
H
-pyrrolo[3,2,1-
ij
]quinolin-2(1
H
)-ones.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070428021100043</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7785-3595</orcidid><orcidid>https://orcid.org/0000-0002-4277-5838</orcidid><orcidid>https://orcid.org/0000-0002-0426-4789</orcidid><orcidid>https://orcid.org/0000-0002-9859-6476</orcidid><orcidid>https://orcid.org/0000-0002-6576-0305</orcidid><orcidid>https://orcid.org/0000-0002-1819-6414</orcidid><orcidid>https://orcid.org/0000-0001-8167-6093</orcidid><orcidid>https://orcid.org/0000-0001-8161-3586</orcidid><orcidid>https://orcid.org/0000-0002-1865-4032</orcidid></addata></record> |
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source | Springer Link |
subjects | Aldehydes Chemistry Chemistry and Materials Science Diketones Ketones Organic Chemistry Quinoline |
title | Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives |
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