Stereochemistry of electrophilic and nucleophilic substitutions at phosphorus

Author:

Kolodiazhnyi Oleg I.1

Affiliation:

1. Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences , Murmanska Street 1 , Kiev 02094 , Ukraine

Abstract

Abstract Nucleophilic and electrophilic substitutions are the most often applied reactions in organophosphorus chemistry. They are closely interrelated, because in a reacting pair always one reagent is an electrophile, and another nucleophile. The reactions of electrophilic and nucleophilic substitutions at the phosphorus center proceed via the formation of a pentacoordinated intermediate. The mechanism of nucleophilic substitution involves the exchange of ligands in the pentacoordinate phosphorane intermediate, leading to the more stable stereomer under the thermodynamic control. Electrophilic substitution proceeds with retention of absolute configuration, whereas nucleophilic substitution with inversion of configuration at the phosphorus center.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Reference53 articles.

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2. O. I. Kolodiazhnyi. Asymmetric Synthesis in Organophosphorus Chemistry. Synthetic Methods, Catalysis and Application, Wiley-VCH, Weinheim (2016).

3. O. I. Kolodiazhnyi, A. O. Kolodiazhna. Stereoselective Synthesis of Organophosphorus Compounds, Naukova Dumka Pbl., Kiev (2017).

4. A. O. Kolodiazhna, O. I. Kolodiazhnyi. Phosphorus Sulfur Silicon192, 621 (2017).

5. O. I. Kolodiazhnyi, A. O. Kolodiazhna. Tetrahedron: Asymmetry28, 1651 (2017).

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