Catalyst‐ and Solvent‐Free Hydrophosphorylation of Aldimines with Secondary Phosphine Chalcogenides: Synthesis of Tertiary <i>α</i> ‐Aminophosphine Oxides, Sulfides and Selenides-Reference-Cited by-同舟云学术

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

Published:2022-12 Issue:45 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
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Author:

Arbuzova Svetlana N.¹,Verkhoturova Svetlana I.¹,Zinchenko Sergey V.¹,Kolyvanov Nikita A.¹,Chernysheva Nataliya A.¹,Bishimbaeva Gaukhar K.²,Trofimov Boris A.¹^ORCID

Affiliation:

1. A. E. Favorsky Irkutsk Institute of Chemistry Siberian Branch Russian Academy of Sciences 1 Favorsky Str. 664033 Irkutsk Russian Federation

2. D. V. Sokolskiy Institute of Fuel, Catalysis and Electrochemistry 142 ul. Kunaeva 050010 Almaty, Republic of Kazakhstan

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202202757

Reference144 articles.

2. A mild and efficient copper-catalyzed coupling of aryl iodides and thiols using an oxime–phosphine oxide ligand

3. Air-Stable, Recyclable, and Regenerative Phosphine Sulfide Palladium(0) Catalysts for C−C Coupling Reaction

4. Triphenylphosphine chalcogenides as efficient ligands for room temperature palladium(II)-catalyzed Suzuki–Miyaura reaction

5. Gadolinium chelate with DO3A conjugated 2-(diphenylphosphoryl)-ethyldiphenylphosphonium cation as potential tumor-selective MRI contrast agent

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