Publications
[60] An Investigation into the Allylic Imidate Rearrangement of Trichloroacetimidates Catalysed by Cobalt Oxazoline Palladacycles.
H. Nomura and C. J. Richards, Chem. Eur. J. 2007, 13, 10216.
 
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[59] An Investigation into the Diastereoselective Palladation of Oxazoline Appended Cobalt Metallocenes.
M. R. Yeamine and C. J. Richards, Tetrahedron: Asymmetry, 2007, 18, 2618.
 
 
[58] Synthesis and Crystal Structures of the First C2-Symmetric Bis-aldimine NCN-Pincer Complexes of Platinum and Palladium.
J. S. Fossey, M. L. Russell, K. M. A. Malik and C. J. Richards, J. Organomet. Chem., 2007, 692, 4843.
 
[57] Chiral Pincer Complexes and Their Application to Asymmetric Synthesis.
C. J. Richards and J. S. Fossey, in The Chemistry of Pincer Type Complexes, ed D. Morales-Morales and C. M. Jensen, Elsevier, Ameterdam, 2007.
 

[56] A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis,
H. V. Nguyen, M. Motevalli and C. J. Richards, Synlett, 2007, 725.

 
[55] Preparation of (h5-(S)-2-(4-Methylethyl)oxazolinylcyclopentadienyl)(h4-tetraphenylcyclobutadiene)cobalt.
C. E. Anderson, L. E. Overman, C. J. Richards, M. P. Watson and N. White, Organic Syntheses, 2007, 84, 139.
 
[54] Preparation of the COP Catalysts: [(S)-COP-OAc]2, [(S)-COP-Cl]2, and (S)-COP-hfacac.
C. E. Anderson, S. F. Kirsch, L. E. Overman, C. J. Richards and M. P. Watson, Organic Syntheses, 2007, 84, 148.
 
[53] Synthesis of planar chiral cobalt metallocenes by microwave-assisted diastereoselective complexation.
C. J. Taylor, M. Motevalli and C. J. Richards, Organometallics, 2006, 25, 2899.
 
[52] A metallocene-pyrrolidinopyridine nucleophilic catalyst for asymmetric synthesis.
H. V. Nguyen, D. C. D. Butler and C. J. Richards, Org. Lett. 2006, 8, 769.
 
[51] (R)-4-Hydroxymethyl-2-ferrocenyloxazoline.
S. El-Fayoummy, M. E. Motevalli, C. J. Richards and M. H. Todd, Acta Cryst E., 2006, E62, m719-m720.
 
[50] Exploiting Planar Chirality for the Generation of a-Ferrocenyl Stereogenic Centres.
C. J. Taylor, F. X. Roca and C. J. Richards, Synlett, 2005, 2159.
 
[49] Synthesis of planar chiral phosphapalladacycles by highly enantioselective transcyclopalladation.
F. X. Roca, M. Motevalli and C. J. Richards, J. Am. Chem. Soc. 2005, 127, 2388.
 
[48] Synthesis of tert-leucine derived cobalt oxazoline palladacycles. Reversal of palladation diastereoselectivity and application to the asymmetric rearrangement of N-aryl trifluoroacetimidates.
R. S. Prasad, C. E. Anderson, C. J. Richards and L. E. Overman, Organometallics, 2005, 24, 77.
 
[47] Synthesis and X-ray crystal structure analysis of the first nickel bisoxazoline pincer complex.
J. S. Fossey and C. J. Richards, J. Organomet. Chem. 2004, 689, 3056.
 
[46] Direct platination as a route to conformationally restricted enantiopure C2-symmetric pincer complexes.
J. S. Fossey, G. Jones, H. V. Nguyen, C. J. Richards, M. A. Stark and H. V. Taylor, Tetrahedron: Asymmetry, 2004, 15, 2067.
 
[45] (S)-Serine derived N-O and N-P oxazoline ligands for asymmetric catalysis.
G. Jones and C. J. Richards, Tetrahedron: Asymmetry, 2004, 15, 653.
 
[44] Synthesis of 2,6-bis(2-oxazolinyl)phenylplatinum(II) NCN pincer complexes by direct cyclometallation. Catalysts for carbon-carbon bond formation.
J. S. Fossey and C. J. Richards, Organometallics, 2004, 23, 367.
 
[43] A ferrocene based palladacyclic precatalyst for the Suzuki cross-coupling of aryl chlorides.
F. X. Roca and C. J. Richards, Chem. Commun., 2003, 3003.
 
[42] Catalysis of aldehyde and imine silylcyanation by platinum and palladium NCN-pincer complexes.
J. S. Fossey and C. J. Richards, Tetrahedron Lett., 2003, 44, 8773.
 
[41] Catalytic asymmetric rearrangement of allylic N-aryl trifluoroacetimidates. A useful method for transforming prochiral allylic alcohols to chiral allylic amines.
L. E. Overman, C. E. Owen, M. M. Pavan and C. J. Richards, Org. Lett., 2003, 5, 1809.
 
[40] Synthesis of monodentate ferrocenylphosphines and their application to the palladium catalysed Suzuki reaction of aryl chlorides.
T. E. Picket, F. X. Roca and C. J. Richards, J. Org. Chem., 2003, 68, 2592.
 
[39] A direct route to platinum NCN-pincer complexes derived from 1,3-bis(imino)benzenes and an investigation into their activity as catalysts for carbon-carbon bond formation.
J. S. Fossey and C. J. Richards, Organometallics, 2002, 21, 5259.
 
[38] The synthesis of 1'-substituted derivatives of 1,2,3,4,5-pentaphenylferrocene.
D. C. D. Butler and C. J. Richards, Organometallics, 2002, 21, 5433.
 
[37] Towards novel biolabels: Synthesis of a tagged highly fluoresent Schiff-base aluminium complex.
M. S. J. Briggs, J. S. Fossey, C. J. Richards, B. Scott and J Whately, Tetrahedron Lett, 2002, 43, 5169.
 
[36] Simple phosphinite-oxazoline ligands for asymmetric catalysis.
G. Jones and C. J. Richards, Tetrahedron Lett., 2001, 42, 5553.
 
[35] A rapid approach to ferrocenophanes via ring-closing metathesis.
A. J. Locke, C. Jones and C. J. Richards, J. Organomet. Chem., 2001, 637 - 639, 669.
 
[34] Synthesis of a C3-symmetric ferrocenylphosphine and its application to the Suzuki reaction of aryl chlorides.
T. E. Pickett and C. J. Richards, Tetrahedron Lett., 2001, 42, 3767.
 
[33] Metallocene appended imidazoles displaying virtual planar chirality.
G. Jones and C. J. Richards, Organometallics, 2001, 20, 1251.
 
[32] Diastereoselective synthesis of enantiopure C2-symmetric dihaloferrocenes.
A. J. Locke, T. E. Pickett and C. J. Richards, Synlett, 2001, 141.
 
[31] Planar chiral mimetics. A new approach to ligand design for asymmetric catalysis.
G. Jones, D. C. D. Butler and C. J. Richards, Tetrahedron Lett., 2000, 41, 9351.
 
[30] Cationic 2,6-bis(2-oxazolinyl)phenylpalladium(II) complexes: Catalysts for the asymmetric Michael reaction.
M. A. Stark, G. Jones and C. J. Richards, Organometallics, 2000, 19, 1282.
 
[29] Production of (R)-aminoglutethimide: A new route from 1-chloro-4-nitrobenzene.
M. J. Bunegar, U. C. Dyer, G. R. Evans, R. P. Hewitt, S. W. Jones, N. Henderson, C. J. Richards, S. Sivaprasad, B. M. Skead, M. A. Stark and E. Teale, Org. Pro. R. & D., 1999, 3, 442.
 
[28] The first example of an enantiopure planar chiral hydroxyferrocene ligand.
T. E. Pickett and C. J. Richards, Tetrahedron: Asymmetry, 1999, 10, 4095.
 
[27] Assignment of 1H NMR chemical shifts in 1,2- and 1,1'-disubstituted ferrocenes.
T. E. Pickett and C. J. Richards, Tetrahedron Lett., 1999, 40, 5251.
 
[26] The asymmetric synthesis of [3](1,1')- and [3](1,1')[3](3,3')-ferrocenophanes.
A. J. Locke and C. J. Richards, Organometallics, 1999, 18, 3750.
 
[25] Synthesis and highly diastereoselective palladation of (h5-(S)-2-(4-methylethyl)oxazolinylcyclopenta-dienyl)(h4-tetraphenylcyclobutadiene)cobalt.
A. M. Stevens and C. J. Richards, Organometallics, 1999, 18, 1346.
 
[24] 2-Nitroferrocenyloxazolines: Precursors to nitrofulvenes and derivatives of (pS)- and (pR)-2-aminoferrocenecarboxylic acids.
R. Salter, T. E. Pickett and C. J. Richards, Tetrahedron: Asymmetry, 1998, 9, 4239.
 
[23] Recent advances in the generation of non-racemic ferrocene derivatives and their application to asymmetric synthesis.
C. J. Richards and A. J. Locke, Tetrahedron: Asymmetry, 1998, 9, 2377.
 
[22] Synthesis and X-ray crystal structure analysis of a scalemic C2-symmetric ferrocenophane.
A. J. Locke, C. J. Richards, D. E. Hibbs and M. B. Hursthouse, Tetrahedron: Asymmetry, 1997, 8, 3383.
 
[21] A metallocene molecular gear.
A. M. Stevens and C. J. Richards, Tetrahedron Lett., 1997, 38, 7805.
 
[20] Catalysts for carbon-carbon bond formation.
M. A. Stark and C. J. Richards, Patent application 9709342.1, May 1997.
 
[19] Synthesis and application of cationic 2,6-bis(2-oxazolinyl)phenylpalladium(II) complexes.
M. A. Stark and C. J. Richards, Tetrahedron Letters, 1997, 38, 5881.
 
[18] Organoiron chemistry 1: Ferrocene and dienyl iron tricarbonyl cation chemistry.
C. J. Richards in Transition Metals in Organic Synthesis, A Practical Approach, Ed.: S. E. Gibson, Oxford University Press, 1997, pp 65-97.
 
[17] Asymmetric synthesis of 1- and 1,1'-ferrocenepropanoic acids.
A. J. Locke and C. J. Richards, Tetrahedron Letters, 1996, 37, 7861.
 
[16] Synthesis of phosphinoferrocenyloxazolines. New ligands for asymmetric catalysis.
C. J. Richards and A. W. Mulvaney, Tetrahedron: Asymmetry, 1996, 7, 1419.
 
[15] Addition of silyl enol ethers and silyl ketene acetals to ferrocenylmethyl ethers. Synthesis of precursors to chiral bridged ferrocenophanes.
A. J. Locke, N. Gouti, C. J. Richards, D. E. Hibbs and M. B. Hursthouse, Tetrahedron, 1996, 52, 1461.
 
[14] PdCl2-complexes containing phosphinoferrocenyloxazoline ligands. X-ray crystal structure analysis and application to Grignard cross-coupling.
C. J. Richards, D. E. Hibbs and M. B. Hursthouse, Tetrahedron Lett., 1995, 36, 3745.
 
[13] Synthesis of 2-[2-(diphenylphosphino)ferrocenyl]oxazoline ligands.
C. J. Richards, T. Damalidis, D. E. Hibbs and M. B. Hursthouse, Synlett, 1995, 74.
 
[12] Stereoselective addition of silyl enol ethers to a-ferrocenylcarbenium Ions.
C. J. Richards, D. E. Hibbs and M. B. Hursthouse, Tetrahedron Lett., 1994, 35, 4215.
 
[11] Enantioselective Diels-Alder reactions of enals: Fighting species multiplicity of the catalyst with donor solvents.
D. Sartor, J. Saffrich, G. Helmchen, C. J. Richards and H. Lambert, Tetrahedron: Asymmetry, 1991, 2, 639.
 
[10] The Transition Elements.
C. J. Richards and S. E. Thomas in General and Synthetic Methods Volume 13, Ed.: G. Pattenden, 1992, pp 250-284.
 
[9] Synthesis and reactivity of iron tricarbonyl complexes of vinylketenes, vinylketenimines and vinylallenes.
L. Hill, C. J. Richards, S. P. Saberi and S. E. Thomas, Pure Appl. Chem., 1992, 64, 371.
 
[8] Nucleophilic addition to vinylketenimine complexes. The asymmetric synthesis of carbon quaternary centres.
C. J. Richards and S. E. Thomas, Tetrahedron: Asymmetry, 1992, 3, 143.
 
[7] Structure of a chiral amide derived from a (vinylketenimine)tricarbonyliron(0) complex.
N. W. Alcock, C. J. Richards and S. E. Thomas, Acta Cryst., 1991, C47, 1261.
 
[6] Preparation of tricarbonyl(h4-vinylketene)iron(0) complexes from tricarbonyl(h4-vinyl ketone)iron(0) complexes and their subsequent conversion to tricarbonyl(h4-vinylketenimine)iron(0) Complexes.
N. A. Alcock, C. J. Richards and S. E. Thomas, Organometallics, 1991, 10, 231.
 
[5] Transition metal-stabilised vinylketenes.
L. Hill, C. J. Richards and S. E. Thomas, Pure Appl. Chem., 1990, 62, 2057.
 
[4] Generation of homochiral quaternary carbon centres from (vinylketenimine)-tricarbonyliron(0) complexes.
N. W. Alcock, G. A. Pike, C. J. Richards and S. E. Thomas, Tetrahedron: Asymmetry, 1990, 1, 531.
 
[3] Nucleophilic addition to vinylketene- and vinylketenimine (allenylideneamine)-tricarbonyliron(0) complexes.
L. Hill, C. J. Richards and S. E. Thomas, J. Chem. Soc., Chem. Commun., 1990, 1085.
 
[2] Conversion of (vinylketene)tricarbonyliron(0) complexes to (vinylketenimine)tricarbonyliron(0) complexes.
C. J. Richards and S. E. Thomas, J. Chem. Soc., Chem. Commun., 1990, 307.
 
[1] Conversion of a,b-unsaturated ketone complexes into a,b-unsaturated ketene complexes. N. W. Alcock, T. N. Danks, C. J. Richards and S. E. Thomas, J. Chem. Soc., Chem. Commun., 1989, 21.