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Acetonitrile: an excellent solvent for the 1,1-dichloromethylenation of certain ketones

Tetrahedron letters, 1988, Vol.29 (24), p.3003-3006

1988

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NOVEL C-3 CYCLIC ETHER CEPHALOSPORINS AND THEIR ORALLY ABSORBED PRODRUG ESTERS

The Journal of Antibiotics, 1994/02/25, Vol.47(2), pp.253-256

1994

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Potent, orally active inhibitors of lipoprotein-associated phospholipase A2: 1-(biphenylmethylamidoalkyl)-pyrimidones

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (1), p.51-55

2002

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Synthesis of the 3-acetoxy-7-oxo-1-azabicyclo [3.2.0] hept-2-ene-2-carboxylate system

Tetrahedron letters, 1986, Vol.27 (49), p.6001-6004

1986

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N-1 substituted pyrimidin-4-ones: Novel, orally active inhibitors of lipoprotein-associated phospholipase A2

Bioorganic & medicinal chemistry letters, 2000-11, Vol.10 (22), p.2557-2561

2000

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Potent, orally active inhibitors of lipoprotein-associated phospholipase A 2: 1-(biphenylmethylamidoalkyl)-pyrimidones

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (1), p.51-55

2002

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N-1 substituted pyrimidin-4-ones: novel, orally active inhibitors of lipoprotein-associated phospholipase A 2

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (22), p.2557-2561

2000

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Synthesis and antibacterial activity of some C-3-lactonyl substituted cephalosporins

Bioorganic & medicinal chemistry letters, 1993-11, Vol.3 (11), p.2219-2224

1993

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2,5-dimethoxy-2,5-dihydrofuran: A convenient synthon for a novel mono-protected glyoxal; synthesis of 4-hydroxybutenolides

Tetrahedron letters, 1990, Vol.31 (29), p.4227-4228

1990

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Novel C-2 Substituted Carbapenem Derivatives: Part III. Synthesis and Biological Activity of 2-(Functionalised Ethenyl, Oxyiminomethyl and α-[Hydroxy]benzyl)-Carbapenems

The Journal of Antibiotics, 1997/03/25, Vol.50(3), pp.237-245

1997

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Synthesis and biological activity of new C-6 and C-7 substituted vinyloxyimino-penicillins and -cephalosporins

Journal of the Chemical Society, Perkin Transactions 1, 1995 (12), p.1483

1995

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Olivanic acid analogues. Part 11. Ozonolysis of α-ethylideneazetidinones: ozonide fragmentation to α-amino acid-N-carboxyanhydrides

J. Chem. Soc., Perkin Trans. 1, 1992 (13), p.1577-1581

1992

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Olivanic acid analogues. Part 10. X-Ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes: functional group control of the stereoselectivity of their reduction products using borohydride reagents

Journal of the Chemical Society, Perkin Transactions 1, 1992 (11), p.1305

1992

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The regioselectivity of cycloaddition reactions between diazomethane and 3-vinylcephalosporins

Journal of the Chemical Society, Perkin Transactions 1, 1991 (6), p.1361

1991

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Olivanic acid analogues. Part 7. Lead tetra-acetate oxidation of 3-alkylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylates

Journal of the Chemical Society, Perkin Transactions 1, 1990 (9), p.2553

1990

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The n.m.r. spectra of porphyrins. 13-A ring current model for the porphyrin and chlorin (7,8-dihydroporphyrin) rings

Organic Magnetic Resonance, 1977-06, Vol.9 (6), p.367-373

1977

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Olivanic acid analogues. Part 4. Cycloaddition reactions of p-nitrobenzyl 7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate, and synthesis of the 8-oxo-1-azatricyclo[4.2.0.02,4]octane-2-carboxylate system

Journal of the Chemical Society, Perkin Transactions 1, 1986, p.973

1986

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Synthesis of 4-substituted tetronic acids: multicolanic acid

Journal of the Chemical Society. Chemical communications, 1979 (2), p.81

1979

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Acetonitrile: an excellent solvent for the 1,1-dichloromethylenation of certain ketones

NOVEL C-3 CYCLIC ETHER CEPHALOSPORINS AND THEIR ORALLY ABSORBED PRODRUG ESTERS

Potent, orally active inhibitors of lipoprotein-associated phospholipase A2: 1-(biphenylmethylamidoalkyl)-pyrimidones

Synthesis of the 3-acetoxy-7-oxo-1-azabicyclo [3.2.0] hept-2-ene-2-carboxylate system

N-1 substituted pyrimidin-4-ones: Novel, orally active inhibitors of lipoprotein-associated phospholipase A2

Potent, orally active inhibitors of lipoprotein-associated phospholipase A 2: 1-(biphenylmethylamidoalkyl)-pyrimidones

N-1 substituted pyrimidin-4-ones: novel, orally active inhibitors of lipoprotein-associated phospholipase A 2

Synthesis and antibacterial activity of some C-3-lactonyl substituted cephalosporins

2,5-dimethoxy-2,5-dihydrofuran: A convenient synthon for a novel mono-protected glyoxal; synthesis of 4-hydroxybutenolides

Novel C-2 Substituted Carbapenem Derivatives: Part III. Synthesis and Biological Activity of 2-(Functionalised Ethenyl, Oxyiminomethyl and α-[Hydroxy]benzyl)-Carbapenems

Synthesis and biological activity of new C-6 and C-7 substituted vinyloxyimino-penicillins and -cephalosporins

Olivanic acid analogues. Part 11. Ozonolysis of α-ethylideneazetidinones: ozonide fragmentation to α-amino acid-N-carboxyanhydrides

Olivanic acid analogues. Part 10. X-Ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes: functional group control of the stereoselectivity of their reduction products using borohydride reagents

The regioselectivity of cycloaddition reactions between diazomethane and 3-vinylcephalosporins

Olivanic acid analogues. Part 7. Lead tetra-acetate oxidation of 3-alkylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylates

The n.m.r. spectra of porphyrins. 13-A ring current model for the porphyrin and chlorin (7,8-dihydroporphyrin) rings

Olivanic acid analogues. Part 4. Cycloaddition reactions of p-nitrobenzyl 7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate, and synthesis of the 8-oxo-1-azatricyclo[4.2.0.02,4]octane-2-carboxylate system

Synthesis of 4-substituted tetronic acids: multicolanic acid

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