P. Little

发表

Comparative tumorigenicity of 1-nitropyrene, 1-nitrosopyrene, and 1-aminopyrene administered by gavage to Sprague-Dawley rats.

S. Hecht, K. El-Bayoumy, A. Rivenson, 1988, Cancer research.

4‐Acylamino‐ and 4‐Ureidobenzamides as Melanin‐Concentrating Hormone (MCH) Receptor 1 Antagonists

T. Ulven, J. Receveur, P. Little, 2005 .

Carcinogenicity of quinoline, 4- and 8-methylquinoline and benzoquinolines in newborn mice and rats.

E. LaVoie, S. Sugie, A. Rivenson, 1988, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Low brain CB1 receptor occupancy by a second generation CB1 receptor antagonist TM38837 in comparison with rimonabant in nonhuman primates: A PET study

B. Gulyás, C. Halldin, K. Varnäs, 2014, Synapse.

New derivatives of the 1,2-benzodiazepine ring system

D. Knight, P. Little, 2000 .

1-Aminobenzotriazole functionalisation using directed metallation: new routes to chromanes and chromenes using intramolecular benzyne trapping by alcohols

D. Knight, P. Little, 2000 .

The first efficient method for the intramolecular trapping of benzynes by phenols: a new approach to xanthenes

D. Knight, P. Little, 2001 .

The First High-yielding Benzyne Cyclisation Using a Phenolic Nucleophile: A New Route to Xanthenes

D. Knight, P. Little, 1998 .

Total synthesis of (+)-phorboxazole A, a potent cytostatic agent from the sponge Phorbas sp.

A. Plowright, T. Ye, G. Pattenden, 2003, Organic & biomolecular chemistry.

The First High-Yielding Benzyne Cyclization Using a Phenolic Nucleophile: A New Route to Xanthenes.

D. Knight, P. Little, 1999 .

A New Approach to Dihydrobenzofurans and Dihydrobenzopyrans (Chromans) Based on the Intramolecular Trapping by Alcohols of Benzynes Generated from 7-Substituted-1-aminobenzotriazoles

M. Birkett, D. Knight, P. Little, 2000 .

Double deprotonation of N-Boc-aminobenzotriazole for the preparation of substituted benzyne precursors

D. Knight, P. Little, K. Stanley, 1996 .

6-Acylamino-2-aminoquinolines as potent melanin-concentrating hormone 1 receptor antagonists. Identification, structure-activity relationship, and investigation of binding mode.

Thomas M Frimurer, Trond Ulven, T. Frimurer, 2005, Journal of medicinal chemistry.

6-Acylamino-2-amino-4-methylquinolines as potent melanin-concentrating hormone 1 receptor antagonists: structure-activity exploration of eastern and western parts.

T. Frimurer, T. Högberg, T. Ulven, 2006, Bioorganic & medicinal chemistry letters.

4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists.

Trond Ulven, T. Högberg, T. Ulven, 2004, Bioorganic & medicinal chemistry letters.

Peripheral selectivity of the novel cannabinoid receptor antagonist TM38837 in healthy subjects.

J. V. van Gerven, C. Elling, M. D. de Kam, 2013, British journal of clinical pharmacology.

Long-acting lipidated analogue of human pancreatic polypeptide is slowly released into circulation.

T. Schwartz, B. Holst, C. Elling, 2011, Journal of medicinal chemistry.

Comparative tumor-initiating activity of methylene-bridged and bay-region methylated derivatives of benz[a]anthracene and chrysene.

J. E. Rice, P. Little, K. Jordan, 1988, Carcinogenesis.

A new strategy for the synthesis of chromans and chromenes

D. Knight, P. Little, 1998 .