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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.  |
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[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.
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[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. |
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[56]
A C2-Symmetric Metallocene-Pyrrolidinopyridine
Nucleophilic Catalyst for Asymmetric Synthesis,
H. V. Nguyen, M. Motevalli and C. J. Richards, Synlett,
2007, 725.  |
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[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. |
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[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. |
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[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. |
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[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.  |
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[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.
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[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. |
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[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. |
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[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. |
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[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. |
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[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.
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[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.
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[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. |
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[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.
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[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.
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[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.
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[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.
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[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.
|
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[36]
Simple phosphinite-oxazoline ligands for asymmetric catalysis.
G. Jones and C. J. Richards, Tetrahedron Lett., 2001,
42, 5553.
|
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[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.
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[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.
|
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[33]
Metallocene appended imidazoles displaying virtual planar chirality.
G. Jones and C. J. Richards, Organometallics, 2001,
20, 1251.
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[32]
Diastereoselective synthesis of enantiopure C2-symmetric
dihaloferrocenes.
A. J. Locke, T. E. Pickett and C. J. Richards, Synlett, 2001,
141.  |
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[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.
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[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.
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[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.
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[28]
The first example of an enantiopure
planar chiral hydroxyferrocene ligand.
T. E. Pickett and C. J. Richards, Tetrahedron: Asymmetry,
1999, 10, 4095.
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[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.
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[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.
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[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.
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[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.
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[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.
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[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.
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[21]
A metallocene molecular gear.
A. M. Stevens and C. J. Richards, Tetrahedron Lett., 1997,
38, 7805.
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[20]
Catalysts for carbon-carbon bond formation.
M. A. Stark and C. J. Richards, Patent application 9709342.1, May
1997. |
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[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.
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[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. |
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[17]
Asymmetric synthesis of 1- and 1,1'-ferrocenepropanoic acids.
A. J. Locke and C. J. Richards, Tetrahedron Letters, 1996,
37, 7861.
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[16]
Synthesis of phosphinoferrocenyloxazolines. New ligands for asymmetric
catalysis.
C. J. Richards and A. W. Mulvaney, Tetrahedron: Asymmetry,
1996, 7, 1419.
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[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.
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[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.
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[13]
Synthesis of 2-[2-(diphenylphosphino)ferrocenyl]oxazoline ligands.
C. J. Richards, T. Damalidis, D. E. Hibbs and M. B. Hursthouse, Synlett,
1995, 74.  |
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[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.
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[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.  |
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[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. |
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[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.  |
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[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.  |
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[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. |
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[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. |
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[5]
Transition metal-stabilised vinylketenes.
L. Hill, C. J. Richards and S. E. Thomas, Pure Appl. Chem.,
1990, 62, 2057.  |
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[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.  |
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[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.  |
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[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.  |
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[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.  |
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