P. Ramsden

发表

Phase-transfer-catalyzed alkylation of guanidines by alkyl halides under biphasic conditions: a convenient protocol for the synthesis of highly functionalized guanidines.

R. Batey, D. Powell, P. Ramsden, 2003, The Journal of organic chemistry.

N-Arylsulfonyl-α-amino carboxamides are potent and selective inhibitors of the chemokine receptor CCR10 that show efficacy in the murine DNFB model of contact hypersensitivity.

D. Jeanfavre, N. Moss, Jiang-Ping Wu, 2016, Bioorganic & medicinal chemistry letters.

Quinazolinone derivatives as orally available ghrelin receptor antagonists for the treatment of diabetes and obesity.

Astrid A. Ortiz, Andrea Mcclure, D. Bierer, 2007, Journal of medicinal chemistry.

Exploration of cathepsin S inhibitors characterized by a triazole P1-P2 amide replacement.

E. Hickey, N. Moss, Yancey D. Ward, 2012, Bioorganic & medicinal chemistry letters.

A Novel Resolution Procedure for the Preparation of P-Stereogenic Phosphine Oxides

M. Parvez, B. A. Keay, D. Che, 1999 .

A simple resolution procedure using the Staudinger reaction for the preparation of P-stereogenic phosphine oxides.

M. Parvez, B. A. Keay, D. Che, 2001, The Journal of organic chemistry.

Synthesis of the C(1)–C(8) segment of (+)-acutiphycin

S. Léger, J. Methot, L. Morency, 2002 .

A new class of 5-HT2B antagonists possesses favorable potency, selectivity, and rat pharmacokinetic properties.

Younggi Choi, N. Moss, D. Skow, 2009, Bioorganic & medicinal chemistry letters.

Reassignment of the absolute configuration of the baker's yeast reduction of (±)-ethyl 1-allyl-2-oxocyclopentanecarboxylate

M. Parvez, B. A. Keay, Michael J. Burke, 1999 .