V. Kamath

发表

Chemo-enzymatic synthesis of trimeric sialyl Lewisx pentadecasaccharide

M. Palcic, Yeuk-Chuen Liu, Hong Li, 2002 .

Large-scale chemical and chemo-enzymatic synthesis of a spacer-containing Pk-trisaccharide.

J. M. Gregson, M. Palcic, V. Kamath, 2004, Carbohydrate research.

D‐Ribonolactone and 2,3‐Isopropylidene(D‐Ribonolactone)

V. Kamath, P. Morris, L. Townsend, 2005 .

Alternative route towards the convergent synthesis of a human purine nucleoside phosphorylase inhibitor—forodesine HCl

V. Kamath, J. Xue, P. Morris, 2009 .

Synthesis of analogs of forodesine HCl, a human purine nucleoside phosphorylase inhibitor-Part II.

V. Kamath, J. Xue, J. J. Juarez-Brambila, 2009, Bioorganic & medicinal chemistry letters.

Synthesis of a potent 5'-methylthioadenosine/S-adenosylhomocysteine (MTAN) inhibitor.

V. Kamath, Y. Babu, P. Morris, 2006, Bioorganic & medicinal chemistry letters.

Synthesis of a potent transition-state inhibitor of 5'-deoxy-5'-methylthioadenosine phosphorylase.

V. Kamath, P. Morris, S. Bantia, 2004, Journal of medicinal chemistry.

Use of diethyl squarate for the coupling of oligosaccharide amines to carrier proteins and characterization of the resulting neoglycoproteins by MALDI-TOF mass spectrometry

V. Kamath, O. Hindsgaul, P. Diedrich, 1996, Glycoconjugate Journal.

Synthesis of the acceptor analog αFuc(1→2)αGal-O(CH2)7 CH3: A probe for the kinetic mechanism of recombinant human blood group B glycosyltransferase

M. Palcic, V. Kamath, O. Hindsgaul, 1999, Glycoconjugate Journal.

The Design of Forodesine HCl and Other Purine Nucleoside Phosphorylase Inhibitors

V. Kamath, P. Morris, 2008 .

Development of a Practical Synthesis of a Purine Nucleoside Phosphorylase Inhibitor: BCX-4208

V. Kamath, P. Morris, C. B. Morris, 2009 .

Synthesis of analogs of forodesine HCl, a human purine nucleoside phosphorylase inhibitor-Part II.

V. Kamath, J. Xue, J. J. Juarez-Brambila, 2009, Bioorganic & medicinal chemistry letters.