Literature DB >> 18043811

Phosphinines as ligands in homogeneous catalysis: recent developments, concepts and perspectives.

Christian Müller1, Dieter Vogt.   

Abstract

Phosphinines belong to an intriguing class of phosphorus-containing heterocycles with interesting steric, electronic and coordinating properties. This article focuses on recent developments, concepts and perspectives in the field of phosphinines and phosphinine-based ligands and their application as ligands in homogeneous catalytic reactions.

Entities:  

Year:  2007        PMID： 18043811     DOI： 10.1039/b712456m

Source DB:  PubMed          Journal:  Dalton Trans        ISSN： 1477-9226            Impact factor:   4.390


  6 in total

1.  N-(2-Hydroxy-ethyl)-2-[3-(p-tol-yl)triazen-1-yl]benzamide.

Authors:  Fernando Rocha-Alonzo; Gerardo Aguirre; Miguel Parra-Hake
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-04-08

2.  Highly active and efficient catalysts for alkoxycarbonylation of alkenes.

Authors:  Kaiwu Dong; Xianjie Fang; Samet Gülak; Robert Franke; Anke Spannenberg; Helfried Neumann; Ralf Jackstell; Matthias Beller
Journal:  Nat Commun       Date:  2017-01-25       Impact factor: 14.919

3.  Making the unconventional μ2-P bridging binding mode more conventional in phosphinine complexes.

Authors:  Yuanfeng Hou; Zhongshu Li; Yaqi Li; Peng Liu; Cheng-Yong Su; Florian Puschmann; Hansjörg Grützmacher
Journal:  Chem Sci       Date:  2019-01-21       Impact factor: 9.825

4.  Luminescent Pyrrole-Based Phosphaphenalene Gold Complexes: Versatile Anticancer Tools with Wide Applicability.

Authors:  Valentina Fermi; Elzbieta Regulska; Anna Wolfram; Patrick Wessling; Frank Rominger; Christel Herold-Mende; Carlos Romero-Nieto
Journal:  Chemistry       Date:  2022-04-19       Impact factor: 5.020

5.  An Iron-Catalyzed Route to Dewar 1,3,5-Triphosphabenzene and Subsequent Reactivity.

Authors:  Adam N Barrett; Martin Diefenbach; Mary F Mahon; Vera Krewald; Ruth L Webster
Journal:  Angew Chem Int Ed Engl       Date:  2022-08-09       Impact factor: 16.823

6.  Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines.

Authors:  Thirusangumurugan Senthamarai; Kathiravan Murugesan; Jacob Schneidewind; Narayana V Kalevaru; Wolfgang Baumann; Helfried Neumann; Paul C J Kamer; Matthias Beller; Rajenahally V Jagadeesh
Journal:  Nat Commun       Date:  2018-10-08       Impact factor: 14.919
  6 in total

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