James M. Morrell

ORGN 309-Catalytic asymmetric protocols for the enantioselective synthesis of 3(2H)-furanones

Charles M. Marson, Esra Edaan, James M. Morrell, 2006 .

Evaluation of by disubstituted acridone derivatives as telomerase inhibitors: the importance of G-quadruplex binding.

James M. Morrell, S. Neidle, L. Kèlland, 2004, Bioorganic & medicinal chemistry letters.

Trisubstituted acridine derivatives as potent and selective telomerase inhibitors.

James M. Morrell, G. Chessari, S. Neidle, 2003, Journal of medicinal chemistry.

A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones.

James M. Morrell, D. Davies, S. Coles, 2007, Chemical communications.

Structure-activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase.

James M. Morrell, S. Joel, D. Vigushin, 2007, Bioorganic & medicinal chemistry letters.