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A New Protocol for the In Situ Generation of Aromatic, Heteroaromatic, and Unsaturated Diazo Compounds and Its Application in Catalytic and Asymmetric Epoxidation of Carbonyl Compounds. Extensive Studies To Map Out Scope and Limitations, and Rationalization of Diastereo- and Enantioselectivities

Journal of the American Chemical Society, 2003-09, Vol.125 (36), p.10926-10940

2003

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The small‐molecule formyl peptide receptor biased agonist, compound 17b, is a vasodilator and anti‐inflammatory in mouse precision‐cut lung slices

British journal of pharmacology, 2024-07, Vol.181 (14), p.2287-2301

2024

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Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds

Angewandte Chemie International Edition, 2001-04, Vol.40 (8), p.1430-1433

2001

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New catalysts containing an N-PO structural unit for the asymmetric reduction of ketones

Tetrahedron letters, 1993-10, Vol.34 (44), p.7105-7106

1993

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Design, synthesis and applications of a ketone reduction catalyst containing a phosphinamide combined with a dioxaborolidine unit

Tetrahedron: asymmetry, 1996-11, Vol.7 (11), p.3071-3074

1996

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Stereoelectronic requirements for a new class of asymmetric ketone reduction catalysts containing an NPO structural unit

Tetrahedron: asymmetry, 1994-05, Vol.5 (5), p.801-804

1994

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Studies of the zinc(II) catalysed addition of silyl enol ethers to cyclic enol ethers

Journal of organometallic chemistry, 1993-08, Vol.455 (1), p.C3-C5

1993

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New chiral phosphinamide catalysts for highly enantioselective reduction of ketones

Tetrahedron letters, 1996-04, Vol.37 (16), p.2853-2856

1996

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Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds We thank the EPSRC (K.M.L., M.J.P., J.R.S.), Avecia for the support of a studentship (M.P.), the EU for a Marie Curie Fellowship (E.A.; HPMF-CT-1999-00076), and Sheffield University for financial support. We thank Dr. J. Blacker (Avecia), Dr. R. V. H. Jones (Zeneca Agrochemicals), and Dr. R. Fieldhouse (Zeneca Agrochemicals) for their interest in this work

Angewandte Chemie International Edition, 2001-04, Vol.40 (8), p.1430-1433

2001

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The use of phosphinamide N-protecting groups in the diastereoselective reduction of ketones

Tetrahedron, 1998-07, Vol.54 (30), p.8827-8840

1998

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Phosphinamides catalysts containing a stereogenic phosphorus atom for the asymmetric reduction of ketones by borane

Tetrahedron: asymmetry, 1997-01, Vol.8 (1), p.73-78

1997

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Chiral phosphinamides: new catalysts for the asymmetric reduction of ketones by borane

Journal of the Chemical Society, Perkin Transactions 1, 1998-03 (6), p.1027-1038

1998

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Katalytische asymmetrische Epoxidierung von Aldehyden mit Schwefel-Yliden und in situ hergestellten Diazoverbindungen

Angewandte Chemie, 2001-04, Vol.113 (8), p.1479-1482

2001

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The use of phosphinamide N-protecting groups in the diastereoselective reduction of ketones

Tetrahedron letters, 1997-03, Vol.38 (13), p.2315-2316

1997

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The Impact of Zero Tolerance School Discipline Policies on School Crime Rates: How Suspensions and Expulsions Affect African American and Special Education Students

Studley, Sherry R

2002

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Renewing the Commitment to Individual Rights

Human Rights, 1992-10, Vol.19 (4), p.10-11

Studley, Janet R.

1992

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Economists' Salaries and Lifetime Productivity

Southern economic journal, 1995-10, Vol.62 (2), p.382-393

1995

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The asymmetric reduction of ketones

Chemistry and industry (London), 1994-01 (14), p.552-555

1994

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Katalytische asymmetrische Epoxidierung von Aldehyden mit Schwefel‐Yliden und in situ hergestellten Diazoverbindungen

Angewandte Chemie, 2001-04, Vol.113 (8), p.1479-1482

2001

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Safety in handling materials

Safety engineering, 1932-06, Vol.63, p.255-256

Studley, R S

1932

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Wool a quick asset: its importance increases because the nation steadily consumes more but gradually produces less: automobile trade demands; America has 800,000 owners of sheep about 60 per cent of imported and domestic fleece goes to Boston [Mass.]

American Bankers Association Journal, 1923-12, Vol.16, p.358-359

Studley, R L

1923

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Marketing and financing of wool

Robert L. Studley, 1924. 87 pp, 1924

Studley, R L

1924

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ChemInform Abstract: Zinc(II) Catalyzed Addition of Silyl Enol Ethers to Cyclic Enol Ethers

ChemInform, 1993-11, Vol.24 (47), p.no-no

1993

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ChemInform Abstract: New Catalysts Containing an N-P=O Structural Unit for the Asymmetric Reduction of Ketones

ChemInform, 1994-02, Vol.25 (5), p.no-no

1994

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ChemInform Abstract: Design, Synthesis and Applications of a Ketone Reduction Catalyst Containing a Phosphinamide Combined with a Dioxaborolidine Unit

ChemInform, 1997-03, Vol.28 (12), p.no-no

1997

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A New Protocol for the In Situ Generation of Aromatic, Heteroaromatic, and Unsaturated Diazo Compounds and Its Application in Catalytic and Asymmetric Epoxidation of Carbonyl Compounds. Extensive Studies To Map Out Scope and Limitations, and Rationalization of Diastereo- and Enantioselectivities

The small‐molecule formyl peptide receptor biased agonist, compound 17b, is a vasodilator and anti‐inflammatory in mouse precision‐cut lung slices

Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds

New catalysts containing an N-PO structural unit for the asymmetric reduction of ketones

Design, synthesis and applications of a ketone reduction catalyst containing a phosphinamide combined with a dioxaborolidine unit

Stereoelectronic requirements for a new class of asymmetric ketone reduction catalysts containing an NPO structural unit

Studies of the zinc(II) catalysed addition of silyl enol ethers to cyclic enol ethers

New chiral phosphinamide catalysts for highly enantioselective reduction of ketones

The use of phosphinamide N-protecting groups in the diastereoselective reduction of ketones

Phosphinamides catalysts containing a stereogenic phosphorus atom for the asymmetric reduction of ketones by borane

Chiral phosphinamides: new catalysts for the asymmetric reduction of ketones by borane

Katalytische asymmetrische Epoxidierung von Aldehyden mit Schwefel-Yliden und in situ hergestellten Diazoverbindungen

The use of phosphinamide N-protecting groups in the diastereoselective reduction of ketones

The Impact of Zero Tolerance School Discipline Policies on School Crime Rates: How Suspensions and Expulsions Affect African American and Special Education Students

Renewing the Commitment to Individual Rights

Economists' Salaries and Lifetime Productivity

The asymmetric reduction of ketones

Katalytische asymmetrische Epoxidierung von Aldehyden mit Schwefel‐Yliden und in situ hergestellten Diazoverbindungen

Safety in handling materials

Wool a quick asset: its importance increases because the nation steadily consumes more but gradually produces less: automobile trade demands; America has 800,000 owners of sheep about 60 per cent of imported and domestic fleece goes to Boston [Mass.]

Marketing and financing of wool

ChemInform Abstract: Zinc(II) Catalyzed Addition of Silyl Enol Ethers to Cyclic Enol Ethers

ChemInform Abstract: New Catalysts Containing an N-P=O Structural Unit for the Asymmetric Reduction of Ketones

ChemInform Abstract: Design, Synthesis and Applications of a Ketone Reduction Catalyst Containing a Phosphinamide Combined with a Dioxaborolidine Unit

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