Choline chloride/ urea as mild media for the synthesis of the chromonyl amidodiester fragments and succinimide derivatives

A simple, green protocol has been accomplished for the synthesis of amidoesters 5 a-k in choline chloride/urea (1:2) through multicomponent reaction of 3-formyl chromone, Meldrum's acid, isocyanides and primary alcohols via a domino reaction. Carrying out the reaction using trifluoroethanol led...

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Bibliographic Details
Main Authors: Jamaati, Hoda (Author) , Balalaie, Saeed (Author) , Rominger, Frank (Author)
Format: Article (Journal)
Language:English
Published: 16 August 2019
In: ChemistrySelect
Year: 2019, Volume: 4, Issue: 31, Pages: 9074-9078
ISSN:2365-6549
DOI:10.1002/slct.201901893
Online Access:Verlag, Volltext: https://doi.org/10.1002/slct.201901893
Verlag: https://onlinelibrary.wiley.com/doi/abs/10.1002/slct.201901893
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Author Notes:Hoda Jamaati, Saeed Balalaie, Maryam Kazemi Miraki, Frank Rominger, and Hamid Reza Bijanzadeh
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Summary:A simple, green protocol has been accomplished for the synthesis of amidoesters 5 a-k in choline chloride/urea (1:2) through multicomponent reaction of 3-formyl chromone, Meldrum's acid, isocyanides and primary alcohols via a domino reaction. Carrying out the reaction using trifluoroethanol led to succinimide derivatives 6 a-d. Easy work-up, selectivity, and good to excellent yields are the advantages of this protocol.
Item Description:Gesehen am 03.12.2019
Physical Description:Online Resource
ISSN:2365-6549
DOI:10.1002/slct.201901893