Dichlorophosphoryl Isocyanate: Synthesis, Chemical Reactions, and Biological Activity of its derivatives

Author:

Mekni Nejib Ben Hussein12ORCID,Medini Faten3,Aroua Lotfi Mohamed45

Affiliation:

1. Laboratory of (Bio)Organic Chemistry: Synthesis, Structural and Physico-Chemical Studies (LR99ES14), Department of Chemistry, Faculty of Science of Tunis, El Manar University, 2092, Tunisia

2. Department of Chemistry, College of Science, Qassim University, campus university, King Abdulaziz Road, Al-Malida, 51452-P.O. Box: 6644, Buraydah, Qassim, Kingdom of Saudi Arabia

3. Laboratory of Aromatic and Medicinal Plants, Biotechnology Center of Borj-Cedria, 2050, Carthage University, Tunisia.

4. Laboratory of (Bio)Organic Chemistry: Synthesis, Structural and Physico-Chemical Studies (LR99ES14), Department of Chemistry, Faculty of Science of Tunis, El Manar University, 2092, Tunisia.

5. Department of Chemistry, College of Science, Qassim University, campus university, King Abdulaziz Road, Al-Malida, 51452-P.O. Box: 6644, Buraydah, Qassim, Kingdom of Saudi Arabia.

Abstract

Abstract: Dichlorophosphoryl isocyanate (DCPI) is the most basic and easy phosphoric isocyanate substrate that introduces organic moieties. Synthesized since 1954, the DCPI has a high reactivity toward primary and secondary alkyl, alcohols, phenols, thiols, and amines via the nucleophilic addition reaction on the carbon atom of the isocyanate group. In addition to their synthesis, the resulting products undergo nucleophilic substitutions of the chlorine atoms. Their reactions with nucleophilic and bi-nucleophile reagents yield acyclic and P-heterocyclic compounds, respectively. The resulting compounds have different potential antibacterial, antifungal, and antitumor activities.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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