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Enantiomerically Pure α-Amino Acid Synthesis via Hydroboration−Suzuki Cross-Coupling

Journal of organic chemistry, 2002-03, Vol.67 (6), p.1802-1815

2002

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A Simplified Route to the (R)-Garner Aldehyde and (S)-Vinyl Glycinol

Synthesis (Stuttgart), 1998-12, Vol.1998 (12), p.1707-1709

1998

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exo-Glycal approaches to C-linked glycosyl amino acid synthesis

Chemical communications (Cambridge, England), 1999-08 (16), p.1599-1600

1999

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The total synthesis of (−)-α-kainic acid using titanium-mediated diene metallabicyclisation methodology

Chemical communications (Cambridge, England), 1999-02 (3), p.245-246

1999

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The synthesis of novel amino acids via hydroboration-Suzuki cross coupling

Tetrahedron letters, 1999-07, Vol.40 (28), p.5263-5266

1999

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The identification of α-ketoamides as potent inhibitors of hepatitis C virus NS3-4A proteinase

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (3), p.355-357

2001

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Solution and solid-Phase synthesis of potent inhibitors of hepatitis C Virus NS3 proteinase

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.641-643

2002

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Completely diastereoselective aziridination of α,β-unsaturated acids via intramolecular reaction of 3-acetoxyaminoquinazolin-4(3 H)-ones

Tetrahedron letters, 2002-03, Vol.43 (11), p.2083-2085

2002

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The stereoselective preparation of substituted pyrrolidines using titanium- and zirconium-mediated diene metallabicyclisation methodology: the total synthesis of (−)-α-kainic acid

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000 (19), p.3194-3204

2000

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Ring-opening of chiral N-(3,4-dihydro-4-oxoquinazolin-3-yl)-substituted aziridines (Q ∗-substituted aziridines): access to Q ∗-free chirons

Tetrahedron letters, 1998-01, Vol.39 (5), p.497-500

1998

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Acid-catalysed ring-opening of N-(3, 4-dihydro-4-oxoquinazolin-3-yl)-substituted aziridines: aziridine ring-opening with retention of configuration

Tetrahedron letters, 1998-06, Vol.39 (24), p.4377-4380

1998

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The Design and Synthesis of Potent Inhibitors of Hepatitis C Virus NS3–4A Proteinase

Antiviral chemistry & chemotherapy, 1999-09, Vol.10 (5), p.259-273

1999

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Reagent- and chelation-controlled diastereoselective aziridination of electron-rich alkenes by 3-acetoxyamino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one

Chemical communications (Cambridge, England), 1996 (16), p.1935

1996

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Enantioselective synthesis and absolute configuration of (−)-pulo'upone by asymmetric intramolecular diels-alder reaction

Tetrahedron letters, 1988, Vol.29 (46), p.5885-5888

1988

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Diastereoselective aziridination of alkenes using 3-acetoxyamino-2-(1-hydroxyalkyl)quinazolin-4(3H )-ones in the presence of titanium(IV) tert-butoxide

Journal of the Chemical Society, Perkin Transactions 1, 1998-09 (17), p.2783-2794

1998

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Elaboration of a cyclohexadienyl triflate iron π-complex by palladium-catalysed coupling

Tetrahedron letters, 1996-04, Vol.37 (16), p.2731-2734

1996

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1-(3,4-Dihydro-4-oxoquinazolin-3-yl)aziridines (Q-substituted aziridines): ring-opening reactions with C–N bond cleavage and preparation of Q-free chirons

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000 (18), p.3096-3106

2000

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Approaches to avermectin assembly: Synthesis of the spiroketal system

Tetrahedron letters, 1987, Vol.28 (46), p.5615-5618

1987

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Enantiomerically Pure α-Amino Acid Synthesis via Hydroboration−Suzuki Cross-Coupling

A Simplified Route to the (R)-Garner Aldehyde and (S)-Vinyl Glycinol

exo-Glycal approaches to C-linked glycosyl amino acid synthesis

The total synthesis of (−)-α-kainic acid using titanium-mediated diene metallabicyclisation methodology

The synthesis of novel amino acids via hydroboration-Suzuki cross coupling

The identification of α-ketoamides as potent inhibitors of hepatitis C virus NS3-4A proteinase

Solution and solid-Phase synthesis of potent inhibitors of hepatitis C Virus NS3 proteinase

Completely diastereoselective aziridination of α,β-unsaturated acids via intramolecular reaction of 3-acetoxyaminoquinazolin-4(3 H)-ones

The stereoselective preparation of substituted pyrrolidines using titanium- and zirconium-mediated diene metallabicyclisation methodology: the total synthesis of (−)-α-kainic acid

Ring-opening of chiral N-(3,4-dihydro-4-oxoquinazolin-3-yl)-substituted aziridines (Q ∗-substituted aziridines): access to Q ∗-free chirons

Acid-catalysed ring-opening of N-(3, 4-dihydro-4-oxoquinazolin-3-yl)-substituted aziridines: aziridine ring-opening with retention of configuration

The Design and Synthesis of Potent Inhibitors of Hepatitis C Virus NS3–4A Proteinase

Reagent- and chelation-controlled diastereoselective aziridination of electron-rich alkenes by 3-acetoxyamino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one

Enantioselective synthesis and absolute configuration of (−)-pulo'upone by asymmetric intramolecular diels-alder reaction

Diastereoselective aziridination of alkenes using 3-acetoxyamino-2-(1-hydroxyalkyl)quinazolin-4(3H )-ones in the presence of titanium(IV) tert-butoxide

Elaboration of a cyclohexadienyl triflate iron π-complex by palladium-catalysed coupling

1-(3,4-Dihydro-4-oxoquinazolin-3-yl)aziridines (Q-substituted aziridines): ring-opening reactions with C–N bond cleavage and preparation of Q-free chirons

Approaches to avermectin assembly: Synthesis of the spiroketal system

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