%0 Journal Article %A Zonouzi, Afsaneh %A Hosseinzadeh, Fatemeh %A Karimi, Nastaran %A Mirzazadeh, Roghieh %A Ng, Seik Weng %D 2016 %T Novel Approaches for the Synthesis of a Library of Fluorescent Chromenopyrimidine Derivatives %U https://acs.figshare.com/articles/journal_contribution/Novel_Approaches_for_the_Synthesis_of_a_Library_of_Fluorescent_Chromenopyrimidine_Derivatives/2415847 %R 10.1021/co300141j.s001 %2 https://acs.figshare.com/ndownloader/files/4056994 %K compound %K domino reaction %K Fluorescent Chromenopyrimidine DerivativesA library %K Novel Approaches %K 290 nm %K chromenopyrimidine derivatives %K fluorescence emission intensity %K intramolecular H %X A library of some new fluorescent chromenopyrimidine derivatives has been synthesized by new approaches. Water-promoted and one-pot reaction can produce new dialkylylamino)-5H-chromeno­[2,3-d]­pyrimidin-2-yl) phenols. These compounds can also be produced using domino reaction. Two parallel methods are compared. Novel N-alkyl-N-phenyl-5H-chromeno­[2,3-d]-pyrimidin-4-amines and 4-alkoxy-5H-chromeno­[2, 3-d]­pyrimidines are synthesized by Lewis-acid catalyzed reactions. The fluorescence emission intensity of the four compounds from each of libraries after excitation in 290 nm is measured. Compound 2-(4,5-bis­(N-methyl-N-phenylamino)-5H-chromeno­[2,3-d]­pyrimidin-2-yl)­phenol was isolated as a byproduct. The details of an interesting exchangeable intramolecular H- bonding of two of the new compounds are reported by X-ray analysis data. %I ACS Publications