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Department of
Biochemistry and Microbiology
76 Lipman Drive - Room 131
New Brunswick, NJ 08901-8525
(732) 932-9763 x131
Fax: (732) 932-8965
E-mail: vanes@aesop.rutgers.edu |
Professor
B.S.
(Chemistry/Physics), University of Witwatersrand (South Africa), 1954
B.S. (Chemistry), University of Witwatersrand (South Africa), 1954
Ph.D. (Organic Chemistry), University of Witwatersrand (South Africa),
1961
Carbohydrate
chemistry and biochemistry, the application of modified glycosidases
in the synthesis of glycosides, synthetic applications of modified enzymes
in organic solvent media
Research
interests are in i) carbohydrate chemistry and biochemistry e.g., the
application of modified glycosidases in the synthesis of glycosides,
ii) synthetic applications of modified enzymes in organic solvent media,
iii) non-immunogenic enzymes.
Recent
publications
van
Es, T., Staskun,
B. Fernandes, M. 2007. Preparation, X-ray structure and propylaminolysis
of 7.7-Dichloro-5,7 -dihydro-theiro[3,4] pyriden-5-one. J. Chem. Res.
376-376.
van
Es, T., Staskun, B. Piggot, A. 2006. The Synthesis of 4-Ethyl-2-propyl-3-substituted-pyrrolo
[3,4-b] quinoline-1,9-dione derivatives from 3,3,-Dichloro-4-ethyl-thien
[3,4-b] quinoline-1,9-dione and Propylamine. S.Afr. J. Chem. 59: 101-108
Carlton,
L. , Staskun B., and van Es, T. 2005. Magnetic Resonance
in Chemistry. A Nitrogen-15 NMR study of hydrogen bonding in 1-Alkl-4-Imino-1,4,-Dihdyro-3-quinolinecarboxylic
acids and related compounds.
van
Es, T. and B. Staskun, and MA Fernandes, S. 2003. Production
of q-thioxo-2,3,4,9-tetrahyelro-pryolo [3,4-b] quinoline -1-ore derivatives
from the aminolysii of 3, 3, 9-tricheoroa 3 H-theiro[3,9-b] quinoline
-1-ore. S.Afr. Journal Chem. 56:30-33.
van
Es, T. and B. Staskun. 2003. Chlorine and sulphur-substitued
Pyrrolo [3,4-b] quinoline and related derivatives arising from aminolysis
of 3,3,9-Trichlorothieno [3,4-b]quinolin -1[3,4,]-one. S. Afr. J. Chem.
56:40-46
van
Es, T. and B. Staskun, 2002. Internet version. 1-Alkyl-1,4,-dihydro-4-iminoquinoline-3-carboxylic
acds? Synthesis, structure and properties. S. Afr. J. Chem. 55:13-33