DR. MADDI SRIDHAR REDDY
 
...




Senior Scientist (CSIR-CDRI)/Assistant Professor (AcSIR)
Medicinal & Process Chemistry Division
Central Drug Research Institute
Lucknow 226 001
 
Educational Qualifications M.Sc., Ph.D.
Phone No. 91-0522-2612411-18 Ext 4379, Mobile: 91-7897582222
E- mail msreddy@cdri.res.in
sridharreddymaddi@yahoo.com
Date of Birth 25-02-1978
 
EDUCATION AND AWARDS
 
Post-Doctoral Research
  Prof. Pierre Deslongchamps’ Laboratory, Department of Chemistry
University of Sherbrooke, Sherbrooke, Quebec, Canada- Mar 2007- Jan 2009 (2 years)

Prof. Pierre Deslongchamps’ Laboratory, Omega Chem Labs, Levis, Quebec, Canada-Jan 2009-Dec 2010 (2 years)

Doctor of Philosophy (Chemistry) : Osmania University 2007
  Doctoral Research was carried out at Indian Institute of Chemical Technology, Hyderabad, India, 2001- 2006 (6 years).
Master of Science (Organic Chemistry): Osmania University, Hyderabad, Andhra Pradesh, India, 1998-2000
 
RESEARCH GROUP
 
    Yalla Kiran Kumar (JRF) (Graduate Student)
    Nuligonda Tirupathi (JRF)  (Graduate Student)
    Mandala Hari Babu (JRF) (Graduate Student)
    Anuradha (Technical Assistant)
    Sabir Shaik (M. Sc. Program)
     
    RESEARCH AREAS
     
    Organo Metallic Reactions, Organo Catalysis, Asymmetric Synthesis and Applications in Medicinal Chemistry
     
    SELECTED PUBLICATIONS
     

    “A New Synthesis of γ-Butyrolactones via AuCl3- or Hg(II)-Catalyzed Intramolecular Hydroalkoxylation of 4-Bromo-3-yn-1-ols”.
    M. Sridhar reddy, Y. Kiran Kumar, N. Thirupathi. Org. Lett. 2012, 14, 824-827.

    “A Quick and Efficient Access to Substituted Quinolines by Electrophilic Cyclization of 1-(2-aminoaryl)-2-yn-1-ols”
    M. Sridhar reddy, Y. Kiran Kumar, N. Thirupathi. RSC Adv. 2012, Just accepted.

    “A Highly Efficient Access to Spiroketals, Mono-unsaturated Spiroketals, and Furans: Hg(II)-Catalyzed Cyclization of Alkyne Diols and Triols”
    K. Ravindar, M. Sridhar Reddy, P. Deslongchamps. Org. Lett., 2011, 13, 3178-3181.

    “Synthesis of the Antiproliferative Agent Hippuristanol and Its Analogues via Suarez Cyclizations and Hg(II)-Catalyzed Spiroketalizations”
    K. Ravindar, M. Sridhar Reddy, L. Lindqvist,  J. Pelletier, P. Deslongchamps. J. Org. Chem., 2011, 76, 1269-1284.
    “Efficient Synthetic Approach to Potent Antiproliferative Agent Hippuristanol via Hg(II)-Catalyzed Spiroketalization”
    K. Ravindar, M. Sridhar Reddy, L. Lindqvist, J. Pelletier, P. Deslongchamps. Org. Lett., 2010, 12 4420-4423.
    Total Synthesis of Ouabagenin and Ouabain
    M. Sridhar Reddy, H. Zhang, S. Phoenix, P. Deslongchamps. Chem. Asian J.     2009, 4, 725-741
    Total Synthesis of Ouabagenin and Ouabain
    H. Zhang, M. Sridhar Reddy, S. Phoenix, P. Deslongchamps. Angew. Chem. Int. Ed., 2008, 47, 1272-1275.
    Total Synthesis of (+)-Cassaine via Transannular Diels-Alder Reaction
    S. Phoenix, M. Sridhar Reddy, P. Deslongchamps. J. Am. Chem. Soc., 2008, 130, 13989-13995.
    A Highly Stereoselective Total Synthesis of Crocacin C via Prins Cyclisation
    J.S.Yadav, M. Sridhar Reddy, P. P.Rao, A.R.Prasad. Synlett 2007, 2049-2052.
    Stereoselective Syntheses of Basiliskamides A and B via Prins Cyclisation”.
    J.S.Yadav, P. P.Rao, M. Sridhar Reddy, A.R.Prasad. Tetrahedron Lett., 2008, 49, 5427-5430.
    Stereoselective Synthesis of (-)-tetrahedronlipstatin via Prins Cyclization”.
    J.S.Yadav, M. Sridhar Reddy, A.R.Prasad. Tetrahedron Lett., 2006, 47, 4995-4998.
    Stereoselective Synthesis of anti-1,3-diol Units via Prins Cyclization: Application to the Synthesis of (-)-Sedamine”.
    J.S.Yadav, M. Sridhar Reddy, P. P.Rao, A.R.Prasad. Tetrahedron Lett., 2006, 47, 4397-4401.
    Stereoselective Synthesis of Polyketide Precursors Containing an anti-1,3-diol System via Prins Cyclization and Reductive Cleavage Sequence”. 
    J.S.Yadav, M. Sridhar Reddy, A.R.Prasad. Tetrahedron Lett., 2006, 47, 4937-4941.
    Enantioselective Synthesis of (+)-Sedamine and (-)-Allosedamine”. 
    J.S.Yadav, M. Sridhar Reddy, P.P.Rao, A.R.Prasad. Synthesis 2006, 4005-4012.
    A Convergent Route to ß-hydroxy δ-lactones Through Prins Cyclization as the key step: Synthesis of (+)-Prelactones B, C and V”.
    J.S.Yadav, M. Sridhar Reddy, A.R.Prasad. Tetrahedron Lett., 2005, 46, 2133-2136