D. Tumelty

发表

Chromatography- and Lyophilization-Free Synthesis of a Peptide-Linker Conjugate

J. Teixeira, Jian Wang, J. Rizzo, 2014 .

Synthesis of a novel analytical reagent for the determination of active sites for conjugation on a catalytic aldolase monoclonal antibody

J. Teixeira, C. Bradshaw, A. Bhat, 2012 .

Solid-phase synthesis of 1,5-benzodiazepin-2-ones

M. Gallop, M. Schwarz, D. Tumelty, 1998 .

Traceless solid-phase synthesis of substituted benzimidazoles via a base-cleavable linker.

C. Holmes, K. Cao, D. Tumelty, 2001, Organic letters.

A Semisynthetic Strategy Leads to Alteration of the Backbone Amidate Ligand in the NiSOD Active Site.

M. Maroney, D. Cabelli, D. Tumelty, 2015, Journal of the American Chemical Society.

Solid-phase synthesis of substituted benzimidazoles

M. Schwarz, M. Needels, K. Cao, 1999 .

Solid-Phase Synthesis of 3,5-Disubstituted 2,3-Dihydro-1,5-benzothiazepin-4(5H)-ones

M. Gallop, M. Schwarz, D. Tumelty, 1999 .

The reduction of aromatic nitro groups on solid supports using sodium hydrosulfite (Na2S2O4)

D. Tumelty, R. Scheuerman, 2000 .

The traceless solid-phase synthesis of organic molecules.

C. Holmes, Yijun Pan, D. Tumelty, 2003, Methods in Enzymology.

Solid-phase synthesis of substituted 1-phenyl-2-aminomethyl-benzimidazoles and 1-phenyl-2-thiomethyl-benzimidazoles

M. Schwarz, M. Needels, D. Tumelty, 1998 .

The Traceless Solid‐Phase Synthesis of Organic Molecules

C. Holmes, Yijun Pan, D. Tumelty, 2005 .

Inhibiting complex IL-17A and IL-17RA interactions with a linear peptide

G. Woodnutt, P. Sahasrabudhe, A. Thorarensen, 2016, Scientific Reports.

Novel α,α-Difluorohomophthalimides via Copper-Catalyzed Tandom Cross-Coupling−Cyclization of 2-Halobenzamides with α,α-Difluoro Reformatskii Reagent

C. Holmes, Yijun Pan, D. Tumelty, 2005 .

A new approach to the chemical synthesis of keto-proteins.

L. Miranda, D. Tumelty, M. Carnevali, 2003, Journal of the American Chemical Society.

Site-specific polymer attachment to a CCL-5 (RANTES) analogue by oxime exchange.

G. Kochendoerfer, L. Miranda, X. Paliard, 2005, Journal of the American Chemical Society.

Combinatorial libraries by light-directed, spatially addressable parallel chemical synthesis: Fidelity of the method and application to drug discovery

A. Sundaram, Valery V. Antonenko, Nicolay Valintovich Kulikov, 1995 .

Immobilised, activated peptides as reagents for cyclic and derivatised peptide libraries

V. Antonenko, D. Vetter, D. Tumelty, 1994 .