A. Campbell

发表

Process Development of a Suzuki Reaction Used in the Manufacture of Lanabecestat

Rebecca E. Meadows, D. Whittaker, M. C. Evans, 2018, Organic Process Research & Development.

Discovery of a series of indan carboxylic acid glycogen phosphorylase inhibitors.

A. Plowright, N. Selmi, P. Kenny, 2010, Bioorganic & medicinal chemistry letters.

Isothiourea‐Catalyzed Atropselective Acylation of Biaryl Phenols via Sequential Desymmetrization/Kinetic Resolution

A. Slawin, Andrew D. Smith, D. Walden, 2020, Angewandte Chemie.

An Isomerization Approach to Tesirine and Pyrrolobenzodiazepines

A. Tiberghien, J. Parker, A. Campbell, 2019, Organic Process Research & Development.

Development and Scale-Up of a Copper-Catalyzed Sulfamidation Coupling Reaction

Simon D. Yates, N. K. Adlington, T. Langer, 2022, Organic Process Research & Development.

The direct synthesis of novel enantiomerically pure α-amino acids in protected form via Suzuki cross-coupling

Philip N. Collier, A. Campbell, R. Taylor, 2000 .

Unified route to the palmarumycin and preussomerin natural products. Enantioselective synthesis of (-)-preussomerin G.

David J. Williams, F. Blaney, A. Barrett, 2002, The Journal of organic chemistry.

Significant rate enhancement via potassium pivalate in a Miyaura borylation approach to verinurad

B. Hayter, A. Campbell, Oliver T. Ring, 2020 .

Synthetic and Chromatographic Challenges and Strategies for Multigram Manufacture of KRASG12C Inhibitors

H. Emtenäs, Anna-Carin C. Carlsson, C. Cook, 2021, Organic Process Research & Development.

The Evolution of High-Throughput Experimentation in Pharmaceutical Development and Perspectives on the Future

Ling Li, Emma McInturff, Ke Wang, 2019, Organic Process Research & Development.

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

T. Raynham, A. Campbell, R. Taylor, 2000 .

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

T. Raynham, A. Campbell, R. Taylor, 1999 .

The design and synthesis of novel, potent and orally bioavailable N-aryl piperazine-1-carboxamide CCR2 antagonists with very high hERG selectivity.

J. Bower, J. G. Cumming, Michael James, 2012, Bioorganic & medicinal chemistry letters.

Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH-Rate Profiles, Autocatalysis, and Disproportionation.

Andrew G. Leach, P. Cox, A. Leach, 2016, Journal of the American Chemical Society.

Studies on the coupling of substituted 2-amino-1,3-oxazoles with chloro-heterocycles

Andrew D. Campbell, J. Pink, Gary M. Noonan, 2012 .

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

T. Raynham, Philip N. Collier, A. Campbell, 2002 .

Hydroboration–Suzuki cross coupling of unsaturated amino acids; the synthesis of pyrimine derivatives

Philip N. Collier, A. Campbell, R. Taylor, 2002 .

THE SYNTHESIS OF NOVEL AMINO ACIDS VIA HYDROBORATION-SUZUKI CROSS COUPLING

T. Raynham, A. Campbell, R. Taylor, 1999 .

Expanding the scope of silane-mediated hydrodehalogenation reactions

G. Lamont, B. Hayter, Benjamin E. Partridge, 2013 .

N-sulfonyloxy carbamates as reoxidants for the tethered aminohydroxylation reaction.

David J. Klauber, T. Donohoe, A. Campbell, 2006, Journal of the American Chemical Society.

Base-Catalyzed Aryl-B(OH)2 Protodeboronation Revisited: From Concerted Proton Transfer to Liberation of a Transient Aryl Anion.

Andrew G. Leach, P. Cox, A. Leach, 2017, Journal of the American Chemical Society.

A critical survey of hydride generation techniques in atomic spectroscopy (Technical Report)

A. Campbell, 1992 .

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

T. Raynham, A. Campbell, D. Paterson, 1999 .

Optimized scale up of 3-pyrimidinylpyrazolo[1,5- a ]pyridine via Suzuki coupling; a general method of accessing a range of 3-(hetero)arylpyrazolo[1,5- a ]pyridines

G. Lamont, Paul A. Bethel, P. Kemmitt, 2012 .

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

T. Raynham, A. Campbell, R. Taylor, 1998 .

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

T. Raynham, A. Campbell, R. Taylor, 1999 .

The synthesis of a dipeptide from its component amino acids: Protecting groups in the elementary organic laboratory

P. Young, A. Campbell, 1982 .

Development and Scale-Up of an Improved Manufacturing Route to the ATR Inhibitor Ceralasertib

Lucinda V. Jackson, A. Dalgleish, Michael Popadynec, 2020, Organic Process Research & Development.

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

T. Raynham, Philip N. Collier, A. Campbell, 2002 .

A redetermination of the sigma constant for the pyridine aza group

R. Shanks, L. Deady, S. Chooi, 1970 .

Exploiting the Physical Properties of Diethanolamine Boronic Esters for Process Improvements in AZD5718

Alexander K. Mullen, David R. J. Hose, P. A. Inglesby, 2023, Organic Process Research & Development.

Process Design and Optimization in the Pharmaceutical Industry: A Suzuki-Miyaura Procedure for the Synthesis of Savolitinib.

G. P. Howell, N. K. Adlington, M. Pilling, 2018, The Journal of organic chemistry.

The synthesis of some substituted methyl pyridinecarboxylates. II. Methyl 4-substituted picolinates, methyl 5-substituted picolinates, and methyl 5-substituted nicotinates

R. Shanks, L. Deady, S. Chooi, 1971 .