Synthesis and structure of new phosphines containing P–N bonds

[1]  A. Slawin,et al.  Synthesis and coordination chemistry of aminophosphine derivatives of adenineElectronic supplementary information (ESI) available: Preparation of all compounds apart from L1 and complex 11; Tables S1?S8: NMR spectral data of all the compounds. See http://www.rsc.org/suppdata/dt/b3/b303715k , 2003 .

[2]  A. Slawin,et al.  Syntheses and Coordination Chemistry of Aminomethylphosphine Derivatives of Adenine , 2003 .

[3]  A. Slawin,et al.  An alternative strategy to an electron rich phosphine based carbonylation catalystThis paper is dedicated to the memory of Prof. Noel McAuliffe in recognition of his contribution to phosphine chemistry and friendship. , 2003 .

[4]  A. Slawin,et al.  The preparation and coordination chemistry of phosphorus(III) derivatives of piperazine and homopiperazine , 2002 .

[5]  A. Slawin,et al.  Synthesis and Coordination Chemistry of the New Unsymmetrical Ligand Ph2PCH2NHC6H4PPh2 , 2002 .

[6]  Gemma L. Holliday,et al.  Highly electron rich alkyl- and dialkyl-N-pyrrolidinyl phosphines: an evaluation of their electronic and structural properties , 2002 .

[7]  A. Slawin,et al.  Synthesis and structure of novel rhodium complexes of multi-functionalised amine-phosphine ligands , 2001 .

[8]  D. Cole-Hamilton,et al.  Synthesis of bulky, electron rich hemilabile phosphines and their application in the Suzuki coupling reaction of aryl chlorides , 2001 .

[9]  M. Beller,et al.  Synthesis of Pyrrolyl-, Indolyl-, and Carbazolylphosphanes and Their Catalytic Application as Ligands in the Hydroformylation of 2-Pentene , 2001 .

[10]  B. Breit,et al.  Phosphabenzenes as monodentate pi-acceptor ligands for rhodium-catalyzed hydroformylation. , 2001, Chemistry.

[11]  A. Spek,et al.  Rhodium complexes based on phosphorus diamide ligands: Catalyst structure versus activity and selectivity in the hydroformylation of alkenes. , 2000 .

[12]  W. Leitner,et al.  Asymmetric Catalysis with Chiral Phosphane/Phosphoramidite Ligands Derived from Quinoline (QUINAPHOS) , 2000 .

[13]  P. V. van Leeuwen,et al.  New phosphacyclic diphosphines for rhodium catalyzed hydroformylation , 1999 .

[14]  K. Goubitz,et al.  Electronic Effect on Rhodium Diphosphine Catalyzed Hydroformylation: The Bite Angle Effect Reconsidered , 1998 .

[15]  Matthias Beller,et al.  Progress in Hydroformylation and Carbonylation , 1995 .

[16]  J. L. Petersen,et al.  N-Pyrrolyl Phosphines: An Unexploited Class of Phosphine Ligands with Exceptional .pi.-Acceptor Character , 1995 .

[17]  D. Powell,et al.  Diphosphines with natural bite angles near 120.degree. increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation , 1992 .

[18]  G. Challa,et al.  A mechanistic study of rhodium tri(o-t-butylphenyl)phosphite complexes as hydroformylation catalysts , 1991 .

[19]  D. Wink,et al.  Practical syntheses of chelating bis(dioxaphospholane) ligands through chlorodioxaphospholane intermediates and demonstration of catalytic competence of bis(phosphite)rhodium cation , 1990 .

[20]  W. R. Moser,et al.  The mechanism of phosphine-modified rhodium-catalyzed hydroformylation studied by CIR-FTIR , 1987 .

[21]  P. V. Leeuwen,et al.  Hydroformylation of less reactive olefins with modified rhodium catalysts , 1983 .

[22]  C. A. Tolman,et al.  Electron donor-acceptor properties of phosphorus ligands. Substituent additivity , 1970 .

[23]  K. Jellinger.  Rhodium Catalysed Hydroformylation , 2003 .

[24]  A. Slawin,et al.  Platinum complexes of tertiary amine functionalised phosphines , 2003 .

[25]  M. Magee,et al.  Electron-Withdrawing Phosphine Compounds in Hydroformylation Reactions. 1. Syntheses and Reactions Using Mono- and Bis(p-toluenesulfonylamino) Phosphines , 2002 .

[26]  A. Slawin,et al.  Synthesis of chelate complexes and the dichalcogen derivatives of the unsymmetrical diphosphine ligand Ph2PNHC6H4PPh2. Molecular structure of [PtCl2(Ph2PNHC6H4PPh2)]·0.75dmso·0.75CHCl3 , 2001 .

[27]  A. Slawin,et al.  P–N bond formation as a route to a highly electron rich bidentate phosphine ligand and its application in homogenous catalysis , 2001 .

[28]  A. Slawin,et al.  P–N bond formation as a route to highly electron rich phosphine ligands , 2000 .

[29]  D. Powell,et al.  Electronically Dissymmetric DIPHOS Derivatives Give Higher n:i Regioselectivity in Rhodium-Catalyzed Hydroformylation Than Either of Their Symmetric Counterparts , 1999 .

[30]  P. V. Leeuwen,et al.  Hydroformylation with a rhodium/bulky phosphite modified catalyst. A comparison of the catlyst behaviour for oct-1-ene, cyclohexene and styrene , 1995 .

[31]  P. V. Leeuwen,et al.  Hydroformylation of oct-1-ene with extremely high rates using rhodium catalysts containing bulky phosphites , 1991 .

[32]  J. D. Unruh,et al.  A study of the mechanism of rhodium/phosphine-catalyzed hydroformylation: use of 1,1′-bis(diarylphosphino)ferrocene ligands , 1982 .

[33]  P. V. Leeuwen,et al.  On the mechanism of the nickel-catalysed regioselective cyclodimerization of isoprene , 1981 .