Zobrazeno 1 - 10
of 13
pro vyhledávání: '"S Lucy, Hind"'
Autor:
and Martin J. Slater, J. Ed Robinson, Martin R. Johnson, Gail Mills, S. Lucy Hind, Tony J. Pateman, Tracy Jane Redfern, David M. Andrews, Paul Spencer Jones, Naimisha Trivedi, Angela Patikis, Michael C. Barnes, Mike D. Dowle
Publikováno v:
Organic Letters. 5:4631-4634
[reaction: see text] In this, the second of two Letters, the optimization of the pyrrolidine-5,5-trans-lactam template (exemplified by 1a) as a mechanism-based inhibitor of hepatitis C NS3/4A protease is described. "Right Box" analysis of cassette do
Autor:
S. Lucy Hind, Gail Mills, Katrina Jane GlaxoSmithKline Wareing, David M. Andrews, Paul Spencer Jones, Martin John Slater, Naimisha Trivedi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:1657-1660
Using the pyrrolidine-5,5- trans -lactam template, we have designed small, neutral, mechanism-based inhibitors of hepatitis C NS3/4A protease. Compound 2b , with a spiro-cyclobutyl P1 substituent and an isopropyl carbonyl substituent at the lactam ni
Autor:
Naimisha Trivedi, Martin R. Johnson, Angela Patikis, David M. Andrews, Paul Spencer Jones, S. Lucy Hind, Mike D. Dowle, Martin John Slater, J. Ed Robinson, Helene M. Chaignot, Coomber Ba, Tony J. Pateman, Gail Mills
Publikováno v:
European Journal of Medicinal Chemistry. 38:339-343
The pyrrolidine-5,5-trans-lactam template was used to design small, neutral, mechanism-based inhibitors of hepatitis C NS3/4A protease displaying potent activity in the replicon cell-based assay. The activity of this series is not dependent upon its
Publikováno v:
Tetrahedron Letters. 41:6897-6900
The indole bis-oxazole 2 , a potential intermediate for the synthesis of the marine natural product diazonamide A 1 , has been synthesised, and attempts to construct the model macrocycle (ring B) 3 are also described; in both approaches rhodium carbe
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :591-600
A new method for the synthesis of oxazoles, and in particular chiral non-racemic oxazoles derived from amino acids, has been developed. Thus, rhodium(II) catalysed reaction of diazocarbonyl compounds 6 and 11 in the presence of amides 8 and 10 result
Publikováno v:
ChemInform. 31
Autor:
Veronique Gouverneur, Christopher David Edlin, Alison Judith Redgrave, Steven P. Nolan, S. Lucy Hind, Catherine A. Slinn
Publikováno v:
ChemInform. 35
Ru- and Mo-based catalysts can be used in ring closing metathesis (RCM) reactions to synthesise cyclic phosphines protected as their borane complexes. The compatibility of the Schrock Mo-catalyst and the N-heterocyclic carbene Ru-catalysts with this
Autor:
Catherine A, Slinn, Alison J, Redgrave, S Lucy, Hind, Chris, Edlin, Steven P, Nolan, Veronique, Gouverneur
Publikováno v:
Organicbiomolecular chemistry. 1(21)
Ru- and Mo-based catalysts can be used in ring closing metathesis (RCM) reactions to synthesise cyclic phosphines protected as their borane complexes. The compatibility of the Schrock Mo-catalyst and the N-heterocyclic carbene Ru-catalysts with this
Autor:
Martin John Slater, David M. Andrews, Paul Spencer Jones, Naimisha Trivedi, Gail Mills, S. Lucy Hind, Katrina Jane GlaxoSmithKline Wareing
Publikováno v:
ChemInform. 34
Using the pyrrolidine-5,5- trans -lactam template, we have designed small, neutral, mechanism-based inhibitors of hepatitis C NS3/4A protease. Compound 2b , with a spiro-cyclobutyl P1 substituent and an isopropyl carbonyl substituent at the lactam ni
Publikováno v:
ChemInform. 31
The indole bis-oxazole 2 , a potential intermediate for the synthesis of the marine natural product diazonamide A 1 , has been synthesised, and attempts to construct the model macrocycle (ring B) 3 are also described; in both approaches rhodium carbe