Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Andrew J. Whitehead"'
Publikováno v:
Green Chemistry. 19:503-510
Halogenated derivatives of phenylalanine can be used as cross-coupling reagents for making drug-like molecules, and pure enantiomers of these precursors are therefore highly desirable. In our exploration of enzymatic routes to simplify the deracemisa
Autor:
Jiasheng Guo, Marie-Catherine Salaun, Greg A. Erickson, Andrew J. Whitehead, Mark B. Mitchell, Mike McClure
Publikováno v:
Tetrahedron Letters. 55:6007-6010
A new synthesis of Lapatinib, an orally active drug for breast cancer, is described. The synthesis involves a palladium catalyzed regioselective arylation of furfural with 6-bromo- N -(3-chloro-4-((3-fluorobenzyl)oxy)phenyl)quinazolin-4-amine. This k
Autor:
Nathalie Langlade, John M. Northall, Alastair J. Roberts, Jonathan P. Graham, Andrew J. Whitehead
Publikováno v:
Organic Process Research & Development. 15:44-48
An efficient and scalable synthesis of a glycine transporter inhibitor is presented. The key steps in the synthetic sequence are the formation of a spirocyclic imidazolidinone from an α-amino nitrile and a cyclic ketone and an arylation of 4-methyl
Publikováno v:
Tetrahedron. 60:2673-2692
The rhodium (I) catalysed tandem hydrosilylation-intramolecular aldol reaction provides a simple strategy for construction of a range of usefully functionalised five-membered rings from readily prepared 6-oxo-2-hexenoates in good yield and with good
Autor:
Andrew J. Whitehead, Nigel S. Simpkins, Robert J. Outram, Alexander J. Blake, Christopher L. Friend
Publikováno v:
Tetrahedron Letters. 42:2877-2881
The reaction of silylketenes with thiophenol, mediated by cinchona alkaloid catalysts, proceeds to give α-silylthioester products in good chemical yield and with enantiomeric excess values in the range 79–93%. The absolute configuration of one of
Stereospecific construction of substituted piperidines. Synthesis of (−)-paroxetine and (+)-laccarin
Publikováno v:
Chem. Commun.. :728-730
Short and efficient enantioselective syntheses of (–)-paroxetine and (+)-laccarin are described based on the highly stereospecific cleavage of C(3)-substituted 1,3-cyclic sulfamidates.
Autor:
Paula J. O'Leary, Michelle Hastings, Philip W. Howard, Patrick McArdle and, James A. S. Howell, Desmond Cunningham, and David A. Owen, and Andrew G. Bell, Andrew J. Whitehead, G. Richard Stephenson
Publikováno v:
Organometallics. 15:4247-4257
A variety of cyclic and acyclic [(pentadienyl)Fe(CO)2L]X complexes (L = CO, PPh3) containing terminal acyloxy or alkoxy substituents have been prepared. In situ NMR studies indicate that for the acyclic series where L = CO, stability is limited by so
Publikováno v:
ChemInform. 22
Autor:
Catherine Mills, Andrew J. Whitehead, David Emiabata‐Smith, William B. Motherwell, A. Mckillop
Publikováno v:
ChemInform. 32
Autor:
Andrew J. Whitehead, Trevor F. Page
Publikováno v:
Thin Solid Films. 220:277-283
In this paper we report the results of ultralow load indentation (“nanoindentation”) tests carried out on a range of thin film coated systems. In addition to characterizing the properties of each system at high resolutions, a further principal ai