Manjula Krishnappa Email & Phone Number | Understanding and studies of reaction mechanisms. Application of those understandings in organic transformations. Development of new, facile and efficient methodologies for Organic transformations. Synthesis of biologically potent molecules predicted by computational methods by rationalizing them via retro synthetic scheme and finding out the expeditious route for the synthesis of such compounds by commercially available reagents. Multi stage synthesis and routine Functional Group transformations. LIST OF PUBLICATIONS 1. K. Manjula, V. P. Jayashankara & M. A. Pasha, Cu-Mg (24:76) alloy: An efficient catalyst for Friedel-Crafts acylation of arenas under microwave irradiation J. Chem. Res (S), 2006, 333-334. 2. M. A. Pasha, K. Manjula and V. P. Jayashankara, Titanium dioxide mediated Friedel-Crafts acylation of aromatic compounds in solvent free conditions under microwave irradiation, Synth. and React. Inorg. Metal-Org. and Nano-Metal Chem., 2006, 36, 321–324. 3. M. A. Pasha and K. Manjula, A simple and an efficient method for the synthesis of δ-chloroesters from tetrahydrofuran and acyl chlorides in the presence of catalytic Iodine Synth. Commun., 2007, 37, 927–932. 4. K. Manjula and M. A. Pasha, Rapid Method of Converting Primary Amides to Nitriles and Nitriles to Primary Amides by ZnCl2 Using Microwaves under Different Reaction Conditions.Synth. Commun., 2007, 37, 1545–1550. 5. K. Manjula and M. A. Pasha, A rapid and efficient method for the synthesis of acylals from aldehydes and their deprotection catalyzed by p-toluenesulphonic acid (p-TSA), Synth. Commun., 2007, 37, 1563–1569. 6. K. Manjula and M. A. Pasha, TiO2: A Simple and an efficient Catalyst for Esterification of Phenols under Solvent- free condition. Indian J Chem. Sec. B, 2008, 47B, 597-600.

Manjula Krishnappa

Understanding and studies of reaction mechanisms. Application of those understandings in organic tr...
Bengaluru, Karnataka, India

*50 free lookup(s) per month.

No credit card required.

Manjula Krishnappa’s Email krishnappam@central.edu

Manjula Krishnappa’s Phone Numbers +1 641-632-****

Get MANJULA’s Phone Number (For Free)

Social Media

Manjula Krishnappa’s Location Bengaluru, Karnataka, India

Manjula Krishnappa’s Current Industry Central College Bangalore

Manjula Krishnappa’s Prior Industry

Not the Manjula Krishnappa you were looking for?

Find accurate emails & phone numbers for over 700M professionals.

Work Experience

Central College

Ph D (Organic chemistry)

Present

Central College Bangalore

Ph.D (Organic Chemistry)

2004-06-01 00:00:00 - Present

Skills

No Skills Available

Languages

No Languages Available

FAQ About Manjula Krishnappa

Manjula Krishnappa is located at
Bengaluru, Karnataka, India

Manjula Krishnappa is a Understanding and studies of reaction mechanisms. Application of those understandings in organic transformations. Development of new, facile and efficient methodologies for Organic transformations. Synthesis of biologically potent molecules predicted by computational methods by rationalizing them via retro synthetic scheme and finding out the expeditious route for the synthesis of such compounds by commercially available reagents. Multi stage synthesis and routine Functional Group transformations. LIST OF PUBLICATIONS 1. K. Manjula, V. P. Jayashankara & M. A. Pasha, Cu-Mg (24:76) alloy: An efficient catalyst for Friedel-Crafts acylation of arenas under microwave irradiation J. Chem. Res (S), 2006, 333-334. 2. M. A. Pasha, K. Manjula and V. P. Jayashankara, Titanium dioxide mediated Friedel-Crafts acylation of aromatic compounds in solvent free conditions under microwave irradiation, Synth. and React. Inorg. Metal-Org. and Nano-Metal Chem., 2006, 36, 321–324. 3. M. A. Pasha and K. Manjula, A simple and an efficient method for the synthesis of δ-chloroesters from tetrahydrofuran and acyl chlorides in the presence of catalytic Iodine Synth. Commun., 2007, 37, 927–932. 4. K. Manjula and M. A. Pasha, Rapid Method of Converting Primary Amides to Nitriles and Nitriles to Primary Amides by ZnCl2 Using Microwaves under Different Reaction Conditions.Synth. Commun., 2007, 37, 1545–1550. 5. K. Manjula and M. A. Pasha, A rapid and efficient method for the synthesis of acylals from aldehydes and their deprotection catalyzed by p-toluenesulphonic acid (p-TSA), Synth. Commun., 2007, 37, 1563–1569. 6. K. Manjula and M. A. Pasha, TiO2: A Simple and an efficient Catalyst for Esterification of Phenols under Solvent- free condition. Indian J Chem. Sec. B, 2008, 47B, 597-600.