Literature DB >> 29299856

Malononitrile dimer as a privileged reactant in design and skeletal diverse synthesis of heterocyclic motifs.

Ahmad Shaabani1, Seyyed Emad Hooshmand2.   

Abstract

Malononitrile dimer as a precursor reactant has been extensively applied in the diversity-oriented synthesis of various heterocyclic motifs, bis-heterocyclic compounds, fused heterocycle derivatives, bicyclic bridged heterocyclic scaffolds, and highly substituted carbocyclic compounds. These remarkable products were synthesized via various types of reactions, such as cycloaddition, cyclocondensation, cascade/domino/tandem reactions along with multi-component reactions. In addition, the flexibility and high reactivity of malononitrile dimer as a multi-functional reagent and its potential to the preparation of novel beneficial scaffolds as well as biologically active molecules signify it as a suitable building block in total synthesis, medicinal chemistry, and dyes. In the present review, the advances in the chemistry of malononitrile dimer as a potent reagent in organic synthesis have been reported in the past to now.

Entities:  

Keywords:  Bioactive molecules; Diversity-oriented synthesis; Heterocyclic compounds; MCRs; Malononitrile dimer; Molecular diversity; Multi-component reactions

Mesh:

Substances:

Year:  2018        PMID: 29299856     DOI: 10.1007/s11030-017-9807-y

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


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