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A One-Pot Fusion of Nitrogen-Containing Heterocycles
ABSTRACT Aromatic and heteroaromatic dialkylaminoaldehydes react with various active methylene compounds in the presence of Me 3 SiCl to give functionally and structurally diverse pyrrolo[1,2-A]quinolines, pyrido[1,2-A]quinolines, pyrazolo[3,4-E]indolizines, pyrazolo[4,3-C]quinolizines, benzo[G]pyrr...
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Published in: | Synthesis (Stuttgart) 2007-09, Vol.2007 (18), p.2872-2886 |
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Language: | English |
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container_end_page | 2886 |
container_issue | 18 |
container_start_page | 2872 |
container_title | Synthesis (Stuttgart) |
container_volume | 2007 |
creator | Ryabukhin, Sergey V. Plaskon, Andrey S. Volochnyuk, Dmitriy M. Shivanyuk, Alexander N. Tolmachev, Andrey A. |
description | ABSTRACT
Aromatic and heteroaromatic dialkylaminoaldehydes react with various active methylene compounds in the presence of Me
3
SiCl to give functionally and structurally diverse pyrrolo[1,2-A]quinolines, pyrido[1,2-A]quinolines, pyrazolo[3,4-E]indolizines, pyrazolo[4,3-C]quinolizines, benzo[G]pyrrolo[1,2-A]-1,8-naphthyridines, and benzo[G]pyrido[1,2-A]-1,8-naphthyridines in high yield and excellent purity. |
doi_str_mv | 10.1055/s-2007-983842 |
format | article |
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Aromatic and heteroaromatic dialkylaminoaldehydes react with various active methylene compounds in the presence of Me
3
SiCl to give functionally and structurally diverse pyrrolo[1,2-A]quinolines, pyrido[1,2-A]quinolines, pyrazolo[3,4-E]indolizines, pyrazolo[4,3-C]quinolizines, benzo[G]pyrrolo[1,2-A]-1,8-naphthyridines, and benzo[G]pyrido[1,2-A]-1,8-naphthyridines in high yield and excellent purity.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-2007-983842</identifier><language>eng</language><ispartof>Synthesis (Stuttgart), 2007-09, Vol.2007 (18), p.2872-2886</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c274t-b602a2e729f39bc5230c36fb00b49a9272bc74ce5ca126128d240ab74eab7d723</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-983842.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2007-983842$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27903,27904,54537,54538</link.rule.ids></links><search><creatorcontrib>Ryabukhin, Sergey V.</creatorcontrib><creatorcontrib>Plaskon, Andrey S.</creatorcontrib><creatorcontrib>Volochnyuk, Dmitriy M.</creatorcontrib><creatorcontrib>Shivanyuk, Alexander N.</creatorcontrib><creatorcontrib>Tolmachev, Andrey A.</creatorcontrib><title>A One-Pot Fusion of Nitrogen-Containing Heterocycles</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>ABSTRACT
Aromatic and heteroaromatic dialkylaminoaldehydes react with various active methylene compounds in the presence of Me
3
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Aromatic and heteroaromatic dialkylaminoaldehydes react with various active methylene compounds in the presence of Me
3
SiCl to give functionally and structurally diverse pyrrolo[1,2-A]quinolines, pyrido[1,2-A]quinolines, pyrazolo[3,4-E]indolizines, pyrazolo[4,3-C]quinolizines, benzo[G]pyrrolo[1,2-A]-1,8-naphthyridines, and benzo[G]pyrido[1,2-A]-1,8-naphthyridines in high yield and excellent purity.</abstract><doi>10.1055/s-2007-983842</doi><tpages>15</tpages></addata></record> |
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title | A One-Pot Fusion of Nitrogen-Containing Heterocycles |
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