S. Rudrawar

发表

Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones

A. Chakraborti, S. Bhagat, S. Rudrawar, 2004 .

Solid-Phase O-Glycosylation with a Glucosamine Derivative for the Synthesis of a Glycopeptide

Philip W Ryan, Anna E. Lohning, Andy Hsien Wei Koh, 2017 .

Lack of correlation between catalytic efficiency and basicity of amines during the reaction of aryl methyl ketones with DMF-DMA: an unprecedented supramolecular domino catalysis.

Dinesh Kumar, A. Chakraborti, A. Sarkar, 2012, Organic & biomolecular chemistry.

O-GlcNAcylation of truncated NAC segment alters peptide-dependent effects on α-synuclein aggregation.

M. Kassiou, Philip W Ryan, A. Davey, 2019, Bioorganic chemistry.

In vitro cytotoxicity of montelukast in HAPI and SH-SY5Y cells.

J. Ekberg, G. Grant, Susan Hall, 2020, Chemico-biological interactions.

Mechanisms underlying select chemotherapeutic‐agent‐induced neuroinflammation and subsequent neurodegeneration

S. Anoopkumar‐Dukie, Fleur A McLeary, A. Davis, 2019, European journal of pharmacology.

Correction: Menaquinone biosynthesis inhibition: a review of advancements toward a new antibiotic mechanism

M. Boersch, S. Rudrawar, M. Zunk, 2018, RSC advances.

Menaquinone biosynthesis inhibition: a review of advancements toward a new antibiotic mechanism

M. Boersch, S. Rudrawar, M. Zunk, 2018, RSC advances.

Solid‐Phase Microwave‐Assisted Ligand‐Free Suzuki‐Miyaura Cross‐Coupling of 5‐Iodouridine

G. Grant, B. Patel, S. Rudrawar, 2018 .

Investigating the Impact of OGT Inhibition on Doxorubicin- and Docetaxel-Induced Cytotoxicity in PC-3 and WPMY-1 Cells

Vivek Makwana, S. Rudrawar, A/Prof Shailendra-Anoopkumar Dukie, 2020, International journal of toxicology.

Scope and limitations of montmorillonite K 10 catalysed opening of epoxide rings by amines

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2004 .

One-Pot Synthesis of 2-Substituted Benzoxazoles Directly from Carboxylic Acids

Dinesh Kumar, A. Chakraborti, S. Rudrawar, 2008 .

Copper(II) tetrafluoroborate as an extremely efficient catalyst for 1,3-dithiolane/dithiane formation from carbonyl compounds under solvent-free conditions at room temperature

A. Chakraborti, S. Rudrawar, R. Besra, 2005 .

An efficient synthesis of 2-amino alcohols by silica gel catalysed opening of epoxide rings by amines.

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2004, Organic & biomolecular chemistry.

Scope and Limitations of Montmorillonite K 10 Catalyzed Opening of Epoxide Rings by Amines.

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2005 .

“On water” organic synthesis: a highly efficient and clean synthesis of 2-aryl/heteroaryl/styryl benzothiazoles and 2-alkyl/aryl alkyl benzothiazolines

S. Chankeshwara, G. Kaur, A. Chakraborti, 2007 .

Simplified Novel Muraymycin Analogues; using a Serine Template Strategy for Linking Key Pharmacophores.

T. Bugg, A. Malde, G. Grant, 2020, ChemMedChem.

Stereoselective Approaches toward the Synthesis of Nucleoside Antibiotic Core Aminoribosyl Glycyluridine

G. Grant, B. Patel, S. Rudrawar, 2019, European Journal of Organic Chemistry.

Lithium Bromide: A Versatile Reagent in Organic Synthesis

S. Rudrawar, 2005 .

Lithium Bromide, an Inexpensive and Efficient Catalyst for Opening of Epoxide Rings by Amines at Room Temperature under Solvent‐Free Condition

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2004 .

Perchloric Acid Adsorbed on Silica Gel (HClO4-SiO2) as an Extremely Efficient and Reusable Catalyst for 1,3-Dithiolane/Dithiane Formation

A. Chakraborti, S. Rudrawar, R. Besra, 2006 .

An Efficient Conversion of Phenolic Esters to Benzothiazoles under Mild and Virtually Neutral Conditions

G. Kaur, Lalima Sharma, A. Chakraborti, 2004 .

An Efficient Acid- and Metal-Free One-Pot Synthesis of Benzothiazoles from Carboxylic Acids

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2005 .

Synthesis and biological evaluation of 2,3-diarylpyrazines and quinoxalines as selective COX-2 inhibitors.

Y. K. Rao, P. Daga, Sunil Singh, 2004, Bioorganic & medicinal chemistry.

An efficient synthesis of C3 C-alkylated Neu5Ac2en derivatives

M. Itzstein, R. Thomson, Mauro Pascolutti, 2013 .

An Efficient Conversion of Phenolic Esters to Benzothiazoles under Mild and Virtually Neutral Conditions.

G. Kaur, Lalima Sharma, A. Chakraborti, 2004 .

Novel furan-2-yl-1H-pyrazoles possess inhibitory activity against α-synuclein aggregation.

M. Kassiou, A. Davey, S. Anoopkumar‐Dukie, 2020, ACS chemical neuroscience.

Synthesis and evaluation of novel 3-C-alkylated-Neu5Ac2en derivatives as probes of influenza virus sialidase 150-loop flexibility.

P. Kerry, R. Russell, J. C. Dyason, 2012, Organic & biomolecular chemistry.

Protection against Radiotherapy-Induced Toxicity

Shailendra Anoopkumar-Dukie, Susan Hall, C. McDermott, 2016, Antioxidants.

Novel sialic acid derivatives lock open the 150-loop of an influenza A virus group-1 sialidase

P. Kerry, R. Russell, J. C. Dyason, 2010, Nature communications.

Atypical group 1 neuraminidase pH1N1-N1 bound to a group 1 inhibitor

G. Gao, J. Qi, Ying Wu, 2015, Protein & Cell.

Novel 3,4-disubstituted-Neu5Ac2en derivatives as probes to investigate flexibility of the influenza virus sialidase 150-loop.

J. C. Dyason, M. von Itzstein, R. Thomson, 2013, Bioorganic & medicinal chemistry.

Signalling transduction of O-GlcNAcylation and PI3K/AKT/mTOR-axis in prostate cancer.

S. Dukie, Vivek Makwana, S. Rudrawar, 2021, Biochimica et biophysica acta. Molecular basis of disease.

Essential role of O-GlcNAcylation in stabilization of oncogenic factors.

S. Dukie, B. Patel, Vivek Makwana, 2019, Biochimica et biophysica acta. General subjects.

The role of sialic acid-binding immunoglobulin-like-lectin-1 (siglec-1) in immunology and infectious disease

T. Haselhorst, S. Kelm, S. Anoopkumar‐Dukie, 2021, International reviews of immunology.

Peptides, Peptidomimetics, and Carbohydrate-Peptide Conjugates as Amyloidogenic Aggregation Inhibitors for Alzheimer's Disease.

Hemant R. Jadhav, M. Kassiou, Philip W Ryan, 2018, ACS chemical neuroscience.

O-GlcNAc Modification Protects against Protein Misfolding and Aggregation in Neurodegenerative Disease.

M. Kassiou, A. Davey, G. Mellick, 2019, ACS chemical neuroscience.

“On Water” Organic Synthesis: A Highly Efficient and Clean Synthesis of 2-Aryl/Heteroaryl/Styryl Benzothiazoles and 2-Alkyl/Aryl Alkyl Benzothiazolines.

S. Chankeshwara, G. Kaur, A. Chakraborti, 2008 .

Advances in the development of imaging probes and aggregation inhibitors for alpha-synuclein

R. Quinn, Hai-Yan Zhang, G. Mellick, 2019, Acta Pharmacologica Sinica.

Caprazamycins: Promising lead structures acting on a novel antibacterial target MraY.

Philip W Ryan, G. Grant, Matthew Zunk, 2019, European journal of medicinal chemistry.

Design, synthesis and bioactivity evaluation of novel pyrazole linked phenylthiazole derivatives in context of antibacterial activity.

G. Grant, B. Patel, S. Rudrawar, 2021, Bioorganic & medicinal chemistry letters.

Novel bisubstrate uridine-peptide analogues bearing a pyrophosphate bioisostere as inhibitors of human O-GlcNAc transferase.

M. von Itzstein, Yun Shi, S. Rudrawar, 2021, Bioorganic chemistry.

Bisubstrate Ether‐Linked Uridine‐Peptide Conjugates as O‐GlcNAc Transferase Inhibitors

A. Malde, S. Anoopkumar‐Dukie, Vivek Makwana, 2020, ChemMedChem.

An Efficient Acid- and Metal-Free One-Pot Synthesis of Benzothiazoles from Carboxylic Acids.

A. Chakraborti, S. Rudrawar, Atul Kondaskar, 2006 .

Liposomal doxorubicin as targeted delivery platform: Current trends in surface functionalization.

T. Haselhorst, S. Anoopkumar‐Dukie, Vivek Makwana, 2020, International journal of pharmaceutics.

4-Substituted Benzylideneisoquinoline-1,3(2H, 4H)-dione Derivatives: Synthesis and Biological Evaluation as Potential HIV-1 Integrase Inhibitors

Hemant R. Jadhav, P. Wadhwa, S. Rudrawar, 2018 .