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One or more keywords matched the following properties of Lakshman, Mahesh
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overview Background Prof. Lakshman obtained the PhD degree from the University of Oklahoma and did postdoctoral work as a Fogarty Fellow at the National Institutes of Health (NIDDK). He then took up an industrial position as Senior Scientist before returning to academia 1998. Prof. Lakshman started his academic career at the University of North Dakota before joining CCNY. From 2008-2011, Prof. Lakshman was the Executive Officer for the CUNY PhD program in Chemistry. Research Prof. Lakshman's research is in organic chemical synthesis pertaining to questions of biological interest. The program has many facets but can be broadly divided into the following areas. A. Nucleoside Modifications. Here new metal-catalyzed as well as uncatalyzed routes are being invented, to enable nucleoside modification. Because nucleosides are highly important in biochemistry, biology, and in medicine, many new methodology is developed and compounds are being synthesized to address biological questions such as design of antiviral and anticancer agents. B. Studies on Environmental Pollutants. In this area, structural and biological effects of DNA modification by environmental pollutants are studied. In addition, new chemical methodology to create model systems for studying metabolic activation processes of environmental pollutants are being developed. C. New Chemical Methodology. New chemical methods to create novel molecules, and new physiologically important molecules are developed. Thus, development of chemical methodology and synthesis of novel molecules require a sound understanding of mechanistic organic chemistry, as being integral to the research.
One or more keywords matched the following items that are connected to Lakshman, Mahesh
Item TypeName
Academic Article O6-(benzotriazol-1-yl)inosine derivatives for C6 modification of purine nucleosides.
Academic Article A simple method for C-6 modification of guanine nucleosides.
Academic Article One-pot etherification of purine nucleosides and pyrimidines.
Academic Article Azide-tetrazole equilibrium of C-6 azidopurine nucleosides and their ligation reactions with alkynes.
Academic Article Palladium-Catalyzed Aryl Amination Reactions of 6-Bromo- and 6-Chloropurine Nucleosides.
Academic Article Direct arylation of 6-phenylpurine and 6-arylpurine nucleosides by ruthenium-catalyzed C-H bond activation.
Academic Article C-C cross-coupling reactions of O6-alkyl-2-haloinosine derivatives and a one-pot cross-coupling/O6-deprotection procedure.
Academic Article Purinyl N1-directed aromatic C-H oxidation in 6-arylpurines and 6-arylpurine nucleosides.
Academic Article Synthesis of N6 ,N6-Dialkyl Adenine Nucleosides With In Situ Formed Hexaalkylphosphorus Triamides.
Academic Article Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products.
Academic Article Correction: Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products.
Academic Article Cladribine Analogues via O6-(Benzotriazolyl) Derivatives of Guanine Nucleosides.
Academic Article Cladribine Analogues via O6-(Benzotriazolyl) Derivatives of Guanine Nucleosides.
Academic Article A novel bis(pinacolato)diboron-mediated N-O bond deoxygenative route to C6 benzotriazolyl purine nucleoside derivatives.
Academic Article Benzimidazopurine nucleosides from N6-aryl adenosine derivatives by PhI(OAc)2-mediated C-N bond formation, no metal needed.
Academic Article Pd-catalyzed versus uncatalyzed, PhI(OAc)2-mediated cyclization reactions of N6-([1,1'-biaryl]-2-yl)adenine nucleosides.
Academic Article Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1H-Benzotriazol-1-yloxy-tris(dimethyl-amino)phosphonium Hexafluorophosphate.
Academic Article Palladium-catalyzed synthesis of carcinogenic polycyclic aromatic hydrocarbon epoxide-nucleoside adducts: the first amination of a chloro nucleoside.
Academic Article Pd-Xantphos-catalyzed direct arylation of nucleosides.
Academic Article Highly diastereoselective synthesis of nucleoside adducts from the carcinogenic benzo[a]pyrene diol epoxide and a computational analysis.
Academic Article O6-(benzotriazol-1-yl)inosine derivatives: easily synthesized, reactive nucleosides.
Academic Article Pd-catalyzed amination of nucleoside arylsulfonates to yield N6-aryl-2,6-diaminopurine nucleosides.
Academic Article Mild and room temperature C-C bond forming reactions of nucleoside C-6 arylsulfonates.
Academic Article A general synthesis of C6-azolyl purine nucleosides.
Academic Article Influence of biaryl phosphine structure on C-N and C-C bond formation.
Academic Article Palladium-catalyzed synthesis of nucleoside adducts from bay- and fjord-region diol epoxides.
Academic Article A novel polymer supported approach to nucleoside modification.
Concept Nucleosides
Concept Purine Nucleosides
Concept Pyrimidine Nucleosides
Academic Article General Approach to N6,C5'-Difunctionalization of Adenosine.
Academic Article Base Modifications of Nucleosides via the Use of Peptide-Coupling Agents, and Beyond.
Academic Article Diversely C8-functionalized adenine nucleosides via their underexplored carboxaldehydes.
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  • Nucleosides
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