P. Reddy

发表

Tetrabenzylpyrophosphate : An Efficient Catalyst for the Synthesis of Carboxamides from Carboxylic Acids and Amines

P. Crooks, Y. Reddy, P. Reddy, 2008 .

Cellulose sulfuric acid: An efficient biodegradable and recyclable solid acid catalyst for the one-pot synthesis of aryl-14H-dibenzo[a.j]xanthenes under solvent-free conditions

P. Crooks, B. Rajitha, J. V. Madhav, 2009 .

Sulfamic Acid: A Novel and Efficient Catalyst for the Synthesis of Aryl-14H-dibenzo[a.j]xanthenes under Conventional Heating and Microwave Irradiation.

B. Rajitha, Y. Reddy, P. Reddy, 2006 .

Diastereoselective Passerini reactions using p-toluenesulfonylmethyl isocyanide (TosMIC) as the isonitrile component

P. Krishna, G. Dayaker, P. Reddy, 2006 .

Sulfamic acid: a novel and efficient catalyst for the synthesis of aryl-14H-dibenzo[a.j]xanthenes under conventional heating and microwave irradiation

B. Rajitha, Y. Reddy, P. Reddy, 2005 .

TiCl4-Catalyzed Efficient One-Pot Synthesis of α α-Amino Phosphonates

Pradeep Kumar Rajput, B. Rajitha, Y. Reddy, 2007 .

Cellulose Sulfuric Acid: An Efficient Biodegradable and Recyclable Solid Acid Catalyst for the One-Pot Synthesis of 3,4-Dihydropyrimidine-2(1H)-ones

P. Crooks, B. Rajitha, Y. Reddy, 2009 .

Copper dipyridine dichloride as a mild and efficient catalyst for a one pot condensation bigenelli reaction

B. Rajitha, P. Someshwar, V. Kumar, 2005 .

An efficient approach towards three component coupling of one pot reaction for synthesis of functionalized benzopyrans

B. Rajitha, N. Srinivasulu, P. S. Kumar, 2006 .

VCL3 CATALYZED EFFICIENT ONE-POT SYNTHESIS OF A-AMINO PHOSPHONATES

B. Rajitha, Y. Reddy, P. Reddy, 2005 .

Synthesis of Biological Active Chromene Benzothiadiazole Derivatives

B. Rajitha, V. Kumar, Y. Reddy, 2005 .

Copper Dipyridine Dichloride as a Mild and Efficient Catalyst for a One-Pot Condensation Biginelli Reaction.

B. Rajitha, P. Someshwar, V. Kumar, 2005 .

Sulfamic acid catalyzed one‐pot synthesis of 2,5‐diaryl‐1,3,4‐oxadiazoles under microwave irradiation and conventional heating

P. Crooks, J. V. Madhav, V. Kumar, 2009 .

Efficient Synthesis of Benzo[g]‐ and Benzo[h]chromene Derivatives by One‐Pot Three‐Component Condensation of Aromatic Aldehydes with Active Methylene Compounds and Naphthols.

B. Rajitha, N. Srinivasulu, P. S. Kumar, 2007 .

Cellulose Sulfuric Acid: Novel and Efficient Biodegradable and Recyclable Acid Catalyst for the Solid-State Synthesis of Thiadiazolo Benzimidazoles

P. Crooks, B. Rajitha, J. V. Madhav, 2011 .

A novel one pot synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes catalyzed by SelectfluorTM under solvent free conditions

B. Rajitha, Y. Reddy, P. Reddy, 2006 .

A novel one pot synthesis of 14-aryl-14H-dibenzo(a,j)xanthenes catalyzed by Selectfluor TM under solvent free conditions

B. Rajitha, Y. Reddy, P. Reddy, 2006 .

Ceric Ammonium Nitrate (CAN): An Efficient Catalyst for the Coumarin Synthesis via Pechmann Condensation using Conventional Heating and Microwave Irradiation

R. S. Dhillon, P. Crooks, C. Baskar, 2008 .

Cellulose Sulfuric Acid: An Efficient Biodegradable and Recyclable Solid Acid Catalyst for the Synthesis of 1-Oxo-hexahydroxanthene

P. Crooks, B. Rajitha, S. V. Laxmi, 2011 .

Bismuth Oxide Perchlorate Catalyzed Efficient Synthesis of 3,4‐Dihydropyrimidin‐2(1H)‐ones: An Improved High Yielding Protocol for the Biginelli Reaction.

G. Rao, B. Rajitha, Y. Reddy, 2005 .

Bismuth Subnitrate Catalyzed Efficient Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones: An Improved Protocol for the Biginelli Reaction.

B. Rajitha, Y. Reddy, P. Reddy, 2005 .

An Efficient Approach Towards Three Component Coupling of One Pot Reaction for Synthesis of Functionalized Benzopyrans.

B. Rajitha, N. Srinivasulu, P. S. Kumar, 2007 .

Efficient Synthesis of Bis(indolyl)methanes Catalyzed by TiCl4.

B. Rajitha, Y. Reddy, P. Reddy, 2005 .

Dipyridine copper chloride catalyzed coumarin synthesis via Pechmann condensation under conventional heating and microwave irradiation

B. Rajitha, P. Someshwar, J. V. Madhav, 2006 .

Expeditious Pechmann Condensation by Using Biodegradable Cellulose Sulfuric Acid as a Solid Acid Catalyst

P. Crooks, B. Rajitha, S. V. Laxmi, 2010 .

SELECTFLUOR™ CATALYZED ONE POT SYNTHESIS OF DIHYDROPYRIMIDINONES: AN IMPROVED PROTOCOL FOR THE BIGINELLI REACTION

B. Rajitha, V. Kumar, Y. Reddy, 2007 .

N‐Methylprolinol Catalysed Asymmetric Baylis−Hillman Reaction

P. Krishna, V. Kannan, P. Reddy, 2004 .

VCl3‐Catalyzed Efficient Synthesis of β‐Enamine Esters and Ketones from β‐Keto Esters.

B. Rajitha, N. Srinivasulu, Y. Reddy, 2006 .

VCl3 Catalysed Efficient Synthesis of β-enamine Esters and Ketones from β-keto Esters

B. Rajitha, N. Srinivasulu, Y. Reddy, 2005 .

Synthesis of Biological Active Chromene Benzothiadiazole Derivatives.

B. Rajitha, V. Kumar, Y. Reddy, 2005 .

Stereoselective total synthesis of (+)-cardiobutanolide and (+)-3-epi-cardiobutanolide from diacetone d-glucose

P. Krishna, P. Reddy, 2006 .

The Baylis–Hillman reaction: a strategic tool for the synthesis of higher-carbon sugars☆

P. Krishna, Aare Sreeshailam, M. U. Kiran, 2007 .

Synthesis of 1-(6-Methylbenzofuran-2-yl)-3-aryl/[4-(β-substituted ethoxy)phenyl]propenones as Marked anti-Microbial Agents.

M. Mannan, Y. Reddy, P. Reddy, 2005 .

The Novel Chemical Entity YTR107 Inhibits Recruitment of Nucleophosmin to Sites of DNA Damage, Suppressing Repair of DNA Double-Strand Breaks and Enhancing Radiosensitization

P. Crooks, W. McDonald, M. Freeman, 2011, Clinical Cancer Research.

Novel substituted (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-diones and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones as potent radio-sensitizing agents.

P. Crooks, M. Freeman, K. Sekhar, 2010, Bioorganic & Medicinal Chemistry Letters.

Cancer Therapy : Preclinical The Novel Chemical Entity YTR 107 Inhibits Recruitment of Nucleophosmin toSites ofDNADamage , SuppressingRepair of DNA Double-Strand Breaks and Enhancing Radiosensitization

P. Crooks, W. McDonald, M. Freeman, 2011 .

Stereoselective total synthesis of (−)-decarestrictine D from l-malic acid ☆

P. Krishna, P. Reddy, 2006 .

SYNTHESIS OF 4,9-DIMETHYL-8- (6-ARYL-2-THIOXO-1,2,3,6-TETRAHYDRO PYRIMIDIN-4-YL)-FURO[2,3-H]CHROMEN-2-ONES AS ANTIMICROBIAL AGENTS UNDER MICROWAVE IRRADIATION

B. Rajitha, P. Reddy, M. K. Rao, 2004 .

A Mild and Efficient Tetrahydropyranylation and Detetrahydropyranylation of Alcohols and Phenols by VCl3

B. Sunil Kumar, B. Rajitha, N. Srinivasulu, 2005 .

Novel substituted (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-diones and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones as potent radio-sensitizing agents.

K. Sekhar, Nidhish Sasi, Y. Reddy, 2010, Bioorganic & medicinal chemistry letters.

Selectfluor™ : A simple and efficient catalyst for the synthesis of substituted coumarins under solvent-free conditions

P. S. Kumar, Y. Reddy, P. Reddy, 2006 .

Vanadium(III) chloride as an effective catalyst for the Pechmann reaction

B. Sunil Kumar, B. Rajitha, N. Srinivasulu, 2006 .