4.4 Article

Catalyst- and Solvent-Free Hydrophosphorylation of Aldimines with Secondary Phosphine Chalcogenides: Synthesis of Tertiary α-Aminophosphine Oxides, Sulfides and Selenides

Journal

CHEMISTRYSELECT
Volume 7, Issue 45, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202202757

Keywords

alpha-aminophosphine chalcogenides; green chemistry; hydrophosphorylation; Schiff bases; secondary phosphine chalcogenides

Funding

  1. Ministry of Education and Science of Russian Federation
  2. Science Committee of the Ministry of Education and Science of the Republic of Kazakhstan
  3. [121021000199-6]
  4. [AP08856550]

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In this study, secondary phosphine chalcogenides reacted mildly with aldimines (without catalysts and solvents, at temperatures of 20-65 degrees Celsius for 0.25-65.5 hours) to yield previously unknown alpha-aminophosphine oxides, sulfides, and selenides in good to excellent yields.
Secondary phosphine chalcogenides mildly (no catalysts and solvents, 20-65 degrees C, 0.25-65.5 h) react with aldimines to deliver the hitherto unknown alpha-aminophosphine oxides, sulfides and selenides in good to excellent yields.

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