A green synthesis of pyrimido[4,5-]quinolines and pyrido[2,3-]pyrimidines a mechanochemical approach
A cost-effective and competent approach has been established for the synthesis of pyrimido[4,5- b ]quinolines and pyrido[2,3- d ]pyrimidines via a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemic...
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Veröffentlicht in: | Organic & biomolecular chemistry 2023-06, Vol.21 (23), p.4854-4862 |
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creator | Singh, Himanshu Kumar Kamal, Arsala Maury, Suresh Kumar Kushwaha, Ambuj Kumar Srivastava, Vandana Singh, Sundaram |
description | A cost-effective and competent approach has been established for the synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill. This transformation involves a one pot, catalyst-free, and solvent-free pathway to develop the desired products under mild reaction conditions.
A green synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill. |
doi_str_mv | 10.1039/d3ob00626c |
format | Article |
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b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill. This transformation involves a one pot, catalyst-free, and solvent-free pathway to develop the desired products under mild reaction conditions.
A green synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
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b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill. This transformation involves a one pot, catalyst-free, and solvent-free pathway to develop the desired products under mild reaction conditions.
A green synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFzrsKwjAYBeAgCtbL4i7kARpNml7oKKL4AG5SSkxSG2mTmOjQt7eo6Oj0H_gOhx-ABcErgmm-FtScMU6jlA9AQOIsQzih-fCbIzwGE--vGJM8S-MAiA28OCk19J2-19IrD00FbedUq4Q5xWGCittDadMoLT1kWrywpyikqPgU3wZbyWumDa9lqzhrILPWGcbrGRhVrPFy_rlTsNzvjtsDcp6Xtl9grit_r9N__gS2eUgg</recordid><startdate>20230614</startdate><enddate>20230614</enddate><creator>Singh, Himanshu Kumar</creator><creator>Kamal, Arsala</creator><creator>Maury, Suresh Kumar</creator><creator>Kushwaha, Ambuj Kumar</creator><creator>Srivastava, Vandana</creator><creator>Singh, Sundaram</creator><scope/></search><sort><creationdate>20230614</creationdate><title>A green synthesis of pyrimido[4,5-]quinolines and pyrido[2,3-]pyrimidines a mechanochemical approach</title><author>Singh, Himanshu Kumar ; Kamal, Arsala ; Maury, Suresh Kumar ; Kushwaha, Ambuj Kumar ; Srivastava, Vandana ; Singh, Sundaram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d3ob00626c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Himanshu Kumar</creatorcontrib><creatorcontrib>Kamal, Arsala</creatorcontrib><creatorcontrib>Maury, Suresh Kumar</creatorcontrib><creatorcontrib>Kushwaha, Ambuj Kumar</creatorcontrib><creatorcontrib>Srivastava, Vandana</creatorcontrib><creatorcontrib>Singh, Sundaram</creatorcontrib><jtitle>Organic & biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Himanshu Kumar</au><au>Kamal, Arsala</au><au>Maury, Suresh Kumar</au><au>Kushwaha, Ambuj Kumar</au><au>Srivastava, Vandana</au><au>Singh, Sundaram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A green synthesis of pyrimido[4,5-]quinolines and pyrido[2,3-]pyrimidines a mechanochemical approach</atitle><jtitle>Organic & biomolecular chemistry</jtitle><date>2023-06-14</date><risdate>2023</risdate><volume>21</volume><issue>23</issue><spage>4854</spage><epage>4862</epage><pages>4854-4862</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>A cost-effective and competent approach has been established for the synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill. This transformation involves a one pot, catalyst-free, and solvent-free pathway to develop the desired products under mild reaction conditions.
A green synthesis of pyrimido[4,5-
b
]quinolines and pyrido[2,3-
d
]pyrimidines
via
a multicomponent reaction of 1,3 diketones (dimedone, barbituric acid, and Meldrum's acid), 6-aminouracil and aromatic aldehyde, through mechanochemical synthesis using a ball-mill.</abstract><doi>10.1039/d3ob00626c</doi><tpages>9</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | A green synthesis of pyrimido[4,5-]quinolines and pyrido[2,3-]pyrimidines a mechanochemical approach |
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