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Development and optimization of simple one-step methods for the synthesis of 4-amino-substituted 1,8-naphthalimides
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Umeå universitet, Medicinska fakulteten, Institutionen för folkhälsa och klinisk medicin, Medicin.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
2014 (Engelska)Ingår i: European Journal of Organic Chemistry, ISSN 1434-193X, E-ISSN 1099-0690, nr 28, s. 6175-6182Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The 1,8-naphthalimide central fragment can be found in a vast number of bioactive compounds and drugs in clinical trials, and can be recognized from their use as fluorescent probes. Of key importance for the fluorescent properties of the scaffold is the 4-amino substituent, which has also proven to be critical in several other chemical and biological applications. Because of the great interest in 1,8-naphthalimides in general, and 4-amino-substituted 1,8-naphthalimides in particular, we have developed and optimized one-step procedures with which to access these derivatives by using an experimental design approach. The multivariate studies of temperature, reaction time, and equivalents of substrates identified conditions with close to quantitative yields that could be applied to generate a range of 4-amino-substituted 1,8-naphthalimides in high yields.

Ort, förlag, år, upplaga, sidor
2014. nr 28, s. 6175-6182
Nyckelord [en]
Oxygen heterocycles, Multicomponent reactions, Nitrogen heterocycles, Synthetic methods, crowave chemistry
Nationell ämneskategori
Organisk kemi
Identifikatorer
URN: urn:nbn:se:umu:diva-95868DOI: 10.1002/ejoc.201402684ISI: 000342842500008OAI: oai:DiVA.org:umu-95868DiVA, id: diva2:770939
Tillgänglig från: 2014-12-11 Skapad: 2014-11-06 Senast uppdaterad: 2018-06-07Bibliografiskt granskad

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Kindahl, TomasChorell, ElinChorell, Erik

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Kindahl, TomasChorell, ElinChorell, Erik
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Kemiska institutionenMedicin
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European Journal of Organic Chemistry
Organisk kemi

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