Unusual acid- and base-catalyzed C-N bond formation approach through reaction of chromonyl Meldrum’s acid and nitrogen binucleophiles

<p>Reaction of chromonyl Meldrum’s acid and N-substituted 2-aminobenzamides was studied in the presence of acidic and basic catalysts. The use of methanesulfonic acid as a catalyst in this reaction led to the synthesis of chromonyl quinazolinones through employing Meldrum’s acid as a carbon le...

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Bibliographic Details
Main Authors: Balalaie, Saeed (Author) , Bijanzadeh, Hamid Reza (Author) , Mehrparvar, Saber (Author) , Rominger, Frank (Author)
Format: Article (Journal)
Language:English
Published: 2016
In: Synlett
Year: 2015, Volume: 27, Issue: 05, Pages: 782-788
ISSN:1437-2096
DOI:10.1055/s-0035-1560383
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1055/s-0035-1560383
Verlag, lizenzpflichtig, Volltext: http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1560383
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Author Notes:Saeed Balalaie, Hamid Reza Bijanzadeh, Saber Mehrparvar, Frank Rominger
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Summary:<p>Reaction of chromonyl Meldrum’s acid and N-substituted 2-aminobenzamides was studied in the presence of acidic and basic catalysts. The use of methanesulfonic acid as a catalyst in this reaction led to the synthesis of chromonyl quinazolinones through employing Meldrum’s acid as a carbon leaving group. However, in the presence of basic catalyst, this reaction gave functionalized 2-pyridones.</p>
Item Description:Published online: 30.11.2015
Gesehen am 19.08.2020
Physical Description:Online Resource
ISSN:1437-2096
DOI:10.1055/s-0035-1560383