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Primary tabs

1. Personal Information

Vincent Paul
National Chemical Laboratory, India

2. Community Expertise

Malaria research
Schistosomiasis research
Chagas Research Community
Toxoplasma Research Community
Tuberculosis research community
The Synaptic Leap community

3. Publications


1. Vincent Paul. A. Sudalai, Thomas Daniel and K. V. Srinivasan. HZSM-5 Catalysed Regiospecific Benzoylation of Activated Aromatic Compounds.,Tetrahedron Lett., 1994, 35, 2601-2602.
2. Vincent Paul. A. Sudalai, Thomas Daniel and K. V. Srinivasan. Regiospecific Bromination of Activated Aromatic Substrates with N-Bromosuccinimide over HZSM-5., Tetrahedron Lett., 1994, 35, 7055-7056.
3. Vincent Paul. A. Sudalai, Thomas Daniel and K. V. Srinivasan. Ultrasound Promoted Bromination of Activated Arenes with N-Bromosuccinimide., Synthetic Commun., 1995, 25, 2401-2405.
4. M. Sasidharan, Satya V. N. Raju, Vincent Paul, K.V. Srinivasan & R. Kumar, Titanium-Silicate Molecular Sieve, TS-1, Catalysed C-C Bond Formation In Mukaiyama Type Aldol Reaction., J. Chem. Soc. Chem. Commun., 1996,129-130.
5. Krisanu Bandyopadhyay, Murali Sastry.Vincent Paul and K. Vijaymohanan, Formation of a Redox Active Self-Assembled Monolayer: Naphtho[1,8-cd]-1,2-dithiol on Gold., Langmuir., 1997, 13, 866-869.
6. Song, G.Y.; Paul, V.; Choo, H.; Morrey, J.; Sidwell, R.W.; Schinazi, R. F.; and Chu, C.K. Enantiomeric Synthesis of D- and L-Cyclopentenyl Nucleosides and their Antiviral Activity Against HIV and West Nile Virus, J. Med. Chem., 2001, 44, 3985-3993).
7. Atul R. Gholap, Vincent Paul* and Kumar V. Srinivasan.* A Novel Process for the synthesis of class I antiarrhythmic agent (±) Cibenzoline and its analogues, Synthetic Communications. (Inpress, 2008)

1) An improved process for the preparation of naphtha [1,8-cd] dithiole. Srinivasan, K.V.,Daniel, T.,Lahoti, R.J.,Swamy, V.P., Rajagopal, R., Application Number: 107/DEL/2001.
2) A process for the preparation of novel disperse dyes from naphtho [1,8-cd]dithiole. Srinivasan, K.V.,Daniel, T.,Lahoti, R.J., Swamy, V.P., Rajagopal, R.,Application Number: 1075/DEL/2000.
3) An improved process for the preparation of imidazolyl compound with high optical purity and the polymorphic form threrof. Joshi, R.A.,Puranik, V.G.,Swamy, V.P.,Shivdshipmi, G.M., Gurjar, M.K.,Barde, A.R.,Bhawal B.M.,Mehta, S.R., CSIR number: NF-357/2004
4) Process for preparing 5,6-Dihydro-4-(S)-(Ethylamino)-6-(S)-methyl-4H-thieno[2,3b]thiopyran-2-sulphonamide,7,7-dioxide HCl. Filed on Dec 2004 Gurjar, M.K.,Deshmukh, M.N., Vincent, P., Radhakrishnan, T.V., Sathe, D.G.,Pardeshi, S.P.,Naik, S.J.,Naik, T.A.,CSIR number : NF-241/2004


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