S. Natarajan

发表

Practical olefin hydroamination with nitroarenes

Thomas E. La Cruz, S. Spergel, W. Pitts, 2015, Science.

Synthesis and biological activity of pyridopyridazin-6-one p38 MAP kinase inhibitors. Part 1.

S. O'keefe, S. Natarajan, R. Tynebor, 2011, Bioorganic & medicinal chemistry letters.

Synthesis and biological activity of pyridopyridazin-6-one p38α MAP kinase inhibitors. Part 2.

S. O'keefe, S. Natarajan, R. Tynebor, 2012, Bioorganic & medicinal chemistry letters.

Synthesis and biological activity of 2H-quinolizin-2-one based p38alpha MAP kinase inhibitors.

S. O'keefe, S. Natarajan, R. Tynebor, 2010, Bioorganic & medicinal chemistry letters.

Asymmetric synthesis via acetal templates. 9. Further studies of the allylation reaction. Preparation of (−)-dihydromyoporone

J. D. Elliott, S. Natarajan, S. Lindell, 1984 .

Enantiospecific synthesis with amino acids. Part 2. α-Alkylation of tryptophan: a chemical and computational investigation of cyclic tryptophan tautomers

J. G. Vinter, S. Natarajan, D. Crich, 1992 .

C—H Oxidation of Ingenanes Enables Potent and Selective Protein Kinase C Isoform Activation

Chien‐Hung Yeh, P. Baran, J. Felding, 2015, Angewandte Chemie.

SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors.

D. Zaller, D. Schmatz, S. O'keefe, 2003, Bioorganic & Medicinal Chemistry Letters.

New Synthetic Technology for the Synthesis of Aryl Ethers: Construction of C-O-D and D-O-E Ring Model Systems of Vancomycin

K. Nicolaou, S. Bräse, C. Boddy, 1997 .

p38MAP kinase inhibitors. Part 1: design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold.

D. Zaller, D. Schmatz, S. O'keefe, 2003, Bioorganic & medicinal chemistry letters.

Synthesis of the taxol AB-system by olefination of an A-ring C1 ketone and direct B-ring closure

S. Natarajan, D. Crich, J. Crich, 1997 .

Total Synthesis of Vancomycin—Part 2: Retrosynthetic Analysis, Synthesis of Amino Acid Building Blocks and Strategy Evaluations

Stefan Bräse, Robert Hughes, Hui Li, 1999 .

Total Synthesis of Vancomycin—Part 1: Design and Development of Methodology

K. Nicolaou, Xin-jie Chu, S. Bräse, 1999 .

1,3-diketones from acid chlorides and ketones: a rapid and general one-pot synthesis of pyrazoles.

S. Natarajan, S. Heller, 2006, Organic letters.

Rapid access to pyrazolo[3,4-c]pyridines via alkyne annulation: limitations of steric control in nickel-catalyzed alkyne insertions.

S. Natarajan, S. Heller, 2007, Organic letters.

Total Synthesis of Vancomycin—Part 4: Attachment of the Sugar Moieties and Completion of the Synthesis

R. Hughes, K. Nicolaou, N. Winssinger, 1999 .

Synthesis of the 2H-quinolizin-2-one scaffold via a stepwise acylation—intramolecular annulation strategy

S. Natarajan, R. Tynebor, Bin Hu, 2006 .

Total Synthesis of Vancomycin Aglycon-Part 2: Synthesis of Amino Acids 1-3 and Construction of the AB-COD-DOE Ring Skeleton.

R. Hughes, K. Nicolaou, T. Bando, 1998, Angewandte Chemie.

Total Synthesis of Vancomycin Aglycon-Part 3: Final Stages.

K. Nicolaou, T. Bando, S. Natarajan, 1998, Angewandte Chemie.

Palladium‐catalyzed hydroxycarbonylation as the key step in the synthesis of a carbon‐14 labeled Maxi‐K channel blocker

M. Braun, S. Natarajan, Luping Liu, 2010 .

p38 MAP kinase inhibitors. Part 5: discovery of an orally bio-available and highly efficacious compound based on the 7-amino-naphthyridone scaffold.

S. O'keefe, K. Vora, S. Natarajan, 2006, Bioorganic & medicinal chemistry letters.

TOTAL SYNTHESIS OF VANCOMYCIN. PART 3 : SYNTHESIS OF THE AGLYCON

R. Hughes, K. Nicolaou, T. Bando, 1999 .

Synthesis of a highly functionalised AB taxane ring system: formation of the eight-membered ring by an efficient 8-exo-tet alkylation of an α-sulfonyl anion

S. Natarajan, D. Crich, 1995 .

Enantiospecific synthesis of amino acids: preparation of (R)- and (S)-α-methylaspartic acid from (S)-tryptophan

S. Natarajan, D. Crich, Chat-On Chan, 1992 .

A Suzuki coupling–macrolactamization approach to the AB-COD bicyclic system of vancomycin

K. Nicolaou, S. Bräse, S. Natarajan, 1997 .

Conformational analysis of substituted hexahydropyrrolo [2,3-b]indoles and related systems. An unusual example of hindered rotation about sulfonamide SN bonds. An X-ray crystallographic and NMR study

M. Bruncko, S. Natarajan, D. Tocher, 1995 .

NEW TECHNOLOGY FOR THE SYNTHESIS OF VANCOMYCIN-TYPE BIARYL RING SYSTEMS

K. Nicolaou, Xin-jie Chu, S. Bräse, 1997 .

Antiovulatory antagonists of LHRH related to antide

G. Flouret, F. Farooqui, S. Natarajan, 1995, Journal of Peptide Science.

Strategies to Build Viable Community Seed System in Dryland Ecosystems for Sustainable Seed and Food Security in India

V. Tonapi, C. R. Reddy, S. Natarajan, 2012 .

p38 MAP kinase inhibitors. Part 6: 2-arylpyridazin-3-ones as templates for inhibitor design.

S. O'keefe, G. Scapin, Suresh B. Singh, 2006, Bioorganic & medicinal chemistry letters.

Evolution of sedentary pastoralism in south India: case study of the Kangayam grassland

Anil . Kumar, S. Natarajan, N. Biradar, 2011 .

1,3‐Diketones from Acid Chlorides and Ketones: A Rapid and General One‐Pot Synthesis of Pyrazoles.

S. Natarajan, S. Heller, 2006 .

P38 MAP kinase inhibitors: evolution of imidazole-based and pyrido-pyrimidin-2-one lead classes.

S. Natarajan, J. Doherty, 2005, Current topics in medicinal chemistry.

p38 MAP kinase inhibitors. Part 3: SAR on 3,4-dihydropyrimido[4,5-d]pyrimidin-2-ones and 3,4-dihydropyrido[4,3-d]pyrimidin-2-ones.

S. O'keefe, S. Natarajan, James E. Thompson, 2006, Bioorganic & medicinal chemistry letters.

Inhibiteurs de la kinase p38 (halo-benzo carbonyl)heterobicyclique

S. Natarajan, J. Stelmach, James B. Doherty, 2003 .