Zobrazeno 1 - 10
of 49
pro vyhledávání: '"C, Cantello"'
Autor:
Nicola C. Stevens, David Haigh, Harshad Kantilal Rami, Barrie C. C. Cantello, Helen C. Birrell, Anantha Ramaswamy, Richard Mark Hindley
Publikováno v:
Tetrahedron: Asymmetry. 10:1335-1351
The synthesis of a new series of potent 2-oxy-3-arylpropanoic acid antihyperglycaemic agents in both racemic and non-racemic form is described. Resolution of racemic acids 1 is accomplished via amide formation with either ( S )-2-phenylglycinol or (
Autor:
David Haigh, Anantha Ramaswamy, Nicola C. Stevens, Barrie C. C. Cantello, Helen C. Birrell, Richard Mark Hindley, R. Curtis Haltiwanger, Drake S. Eggleston
Publikováno v:
Tetrahedron: Asymmetry. 10:1353-1367
Boron-mediated asymmetric aldol reactions of substituted benzaldehyde 5 with 2-oxyethanoyloxazolidinones 4a–e, containing electron withdrawing, chelating, and bulky alkoxy and aryloxy groups, gave variable yields of syn-aldol adducts 6a–e in high
Autor:
David Kenneth Dean, P.J. Coyle, Stephen A. Smith, Harshad Kantilal Rami, Ivan Leo Pinto, Michael A. Cawthorne, Richard Mark Hindley, Derek R. Buckle, Barrie C. C. Cantello, Carolyn A. Lister, David Haigh, Andrew Faller, L. J. Jefcott, D.G. Smith
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2127-2130
The thiazolidine-2,4-dione ring of insulin sensitising antidiabetic agents can be replaced by α-acyl-, α-alkyl- and α-(aralkyl)-carboxylic acids. Inclusion of an additional lipophilic moiety affords compounds 14 and 16, equipotent to BRL 48482.
Non thiazolidinedione antihyperglycaemic agents. 1: α-Heteroatom substituted β-phenylpropanoic acids
Autor:
Barrie C. C. Cantello, Carolyn A. Lister, Andrew Faller, Harshad Kantilal Rami, P.J. Coyle, D.G. Smith, Ivan Leo Pinto, L. J. Jefcott, David Haigh, Michael A. Cawthorne, David Kenneth Dean, Stephen A. Smith, Derek R. Buckle, Richard Mark Hindley
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2121-2126
The 5-benzylthiazolidine-2,4-dione moiety of insulin sensitising antidiabetic agents can be replaced by a range of α-heteroatom functionalised β-phenylpropanoic acids. α-Oxy-carboxylic acids show potent antidiabetic activity and one compound, the
Autor:
Stephen A. Smith, Barrie C. C. Cantello, Peter L. Thurlby, Richard Mark Hindley, Michael A. Cawthorne, David Haigh
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1181-1184
Modifications based upon a metabolite of ciglitazone afforded BRL 49653, a novel potent insulin sensitizer. A facile synthesis of this compound is described.
Autor:
Drake S. Eggleston, Barrie C. C. Cantello, David Haigh, Richard Mark Hindley, Catherine M. Heath, Sime John Thomas, Stefan Roland Woroniecki, Keith R. Jennings, R. Curtis Haltiwanger
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :3319-3324
A novel biotransformation system for the reduction of carbon-carbon double bonds in 5-benzylidenethiazolidine-2, 4-diones, to give the corresponding 5-benzylthiazolidine-2, 4-diones, using whole cells of red yeasts is described. These reduced compoun
Autor:
R. C. Haltiwanger, Sime John Thomas, C. M. Heath, Barrie C. C. Cantello, Drake S. Eggleston, Richard Mark Hindley, Stefan Roland Woroniecki, David Haigh, Keith R. Jennings
Publikováno v:
ChemInform. 26
Autor:
David Kenneth Dean, P.J. Coyle, L. J. Jefcott, Stephen A. Smith, Harshad Kantilal Rami, David Haigh, Michael A. Cawthorne, Barrie C. C. Cantello, Carolyn A. Lister, Andrew Faller, Richard Mark Hindley, Pinto Ivan Leo, Smith David Glynn, Derek R. Buckle
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 28
Autor:
Harshad Kantilal Rami, Nicola C. Stevens, Barrie C. C. Cantello, Helen C. Birrell, David Haigh, Richard Mark Hindley, Anantha Ramaswamy
Publikováno v:
ChemInform. 30
The synthesis of a new series of potent 2-oxy-3-arylpropanoic acid antihyperglycaemic agents in both racemic and non-racemic form is described. Resolution of racemic acids 1 is accomplished via amide formation with either ( S )-2-phenylglycinol or (