Literature DB >> 23547948

Novel approaches for the synthesis of a library of fluorescent chromenopyrimidine derivatives.

Afsaneh Zonouzi1, Fatemeh Hosseinzadeh, Nastaran Karimi, Roghieh Mirzazadeh, Seik Weng Ng.   

Abstract

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.

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Year:  2013        PMID: 23547948     DOI: 10.1021/co300141j

Source DB:  PubMed          Journal:  ACS Comb Sci        ISSN: 2156-8944            Impact factor:   3.784


  3 in total

Review 1.  Transition metal-free one-pot synthesis of nitrogen-containing heterocycles.

Authors:  Simpal Kumari; Dharma Kishore; Sarvesh Paliwal; Rajani Chauhan; Jaya Dwivedi; Aakanksha Mishra
Journal:  Mol Divers       Date:  2015-06-09       Impact factor: 2.943

2.  Novel domino procedures for the synthesis of chromene derivatives and their isomerization.

Authors:  Afsaneh Zonouzi; Zakieh Izakian; Seik Weng Ng
Journal:  Mol Divers       Date:  2016-03-22       Impact factor: 2.943

3.  Steroidal[17,16-d]pyrimidines derived from dehydroepiandrosterone: A convenient synthesis, antiproliferation activity, structure-activity relationships, and role of heterocyclic moiety.

Authors:  Shaoyong Ke; Liqiao Shi; Zhigang Zhang; Ziwen Yang
Journal:  Sci Rep       Date:  2017-03-14       Impact factor: 4.379

  3 in total

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