S. A. Richards

发表

Oxidative β-C–H sulfonylation of cyclic amines† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc04900e

Weiping Kong, E. Talbot, M. Willis, 2018, Chemical science.

Synthesis and pharmacological investigation of azaphthalazinone human histamine H(1) receptor antagonists.

C. Browning, S. Lynn, P. Procopiou, 2012, Bioorganic & medicinal chemistry.

Gel phase MAS 1H NMR as a probe for supramolecular interactions at the solid–liquid interface

N. Bampos, J. Sanders, Y. R. Miguel, 1998 .

Solid phase synthesis of 5-aminopyrazoles and derivatives part II

S. Watson, Richard D. Wilson, S. A. Richards, 1998 .

SOLID PHASE SYNTHESIS OF 5-AMINOPYRAZOLES AND DERIVATIVES

D. Judd, S. Watson, Richard D. Wilson, 1997 .

Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists.

J. Percy, Afjal H. Miah, P. Procopiou, 2014, Bioorganic & medicinal chemistry.

1,4-Benzodiazepin-2-one derived neurokinin-1 receptor antagonists

M. Congreve, P. Ward, A. B. Hawcock, 1997 .

Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating arylsulfonamide groups.

I. McLay, D. Coe, K. Biggadike, 2009, Journal of medicinal chemistry.

2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosis.

S. Hodgson, J. Percy, Lena Shukla, 2016, European journal of medicinal chemistry.

Base catalysed rearrangement of fluocinolone acetonide to a 17α-pregnane-21,16α-carbolactone

S. Lynn, P. Procopiou, S. A. Richards, 2000 .

Synthesis and Structure−Activity Relationships of Long-acting β2 Adrenergic Receptor Agonists Incorporating Arylsulfonamide Groups

I. McLay, D. Coe, K. Biggadike, 2009 .