CHEVULA GURUMURTHY
C/O Dr. G. Sabitha Senior Principal Scientist
CSIR-Indian Institute of Chemical TechnologyHyderabad, 500 007 Telangana, India.
Cell: +91-9177137477
E-mail: gurumurthyiict@gmail.com
ACADEMIC RECORD:
Nov 2017- Post-Doctoral Fellow in Synthetic Organic Chemistry, under the supervision Of Qinghui Zhou Ph.D Professor,
College of Chemistry and Molecular Sciences, Wuhan University in Wuhan, China.
Dec 2010 – May 2016 Ph. D in Synthetic Organic Chemistry, under the supervision of Dr. G. Sabitha,
Senior Principal Scientist, CSIR-Indian Institute of Chemical Technology (IICT), Hyderabad, India.
Thesis Title: “Studies Towards the Synthesis of Pectinolide-F, jimalides A-D and Pyrido[2,3-c]coumarin Derivatives”.
June 2005 – April 2007 Master of Science (M.Sc.), Organic Chemistry, Kakatiya University,
Warangal, India.
June 2002 – April 2005 Bachelor of Science (B.Sc.), SV Degree College, Kodad, Nalgonda, India.
AWARDS AND FELLOWSHIPS:
Awarded Senior Research Fellowship (SRF) from the Council for Scientific and Industrial Research (CSIR), New Delhi, India (Dec 2012-May 2016)
Awarded Junior Research Fellowship (JRF) from the Council for Scientific and Industrial Research (CSIR), New Delhi, India (Dec 2010- Dec 2012)
NET Qualified in 2008 &2010
TEACHING EXPERINCE:
Taught undergraduate and courses at S.V. Degree &P.G College Suryapet, Nalgonda, Telangana, India, June 2008- Dec 2010.
LIST OF PUBLICATIONS:
1. The First Total Synthesis of Pectinolide F
Gowravaram Sabitha,* Chevula Gurumurthy, Jhillu Singh Yadav
( Synthesis 2014, 46, 1757–1764)
2. Studies toward the synthesis of Iejimalides A-D: Synthesis of C3-C11 and C12-C24 fragments
Gowravaram Sabitha,* Chevula Gurumurthy, Jhillu Singh Yadav
(Synthesis 2014, 46, 110–118)
3. A Diastereoselective Synthesis of Tetrahydro- and Dihydro- pyrido[2,3-c]coumarin derivatives via a one-pot Three-Component Povarov Reaction Catalyzed by Bismuth(III) Chloride
Ch. Gurumurthy,a,d Narjis Fatima,a G. Narender Reddy,b C. Ganesh Kumar,b Gowravaram Sabitha,a,* K. V. S. Ramakrishna,c
(Bioorg. Med. Chem. Lett. 2016, 26, 5119–5125)