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FACULTY

Dr. Nagendra G Assistant Professor

School of Applied Sciences

Dr. Nagendra G

Specialization

Organic chemistry, Peptide and Peptidomimetic Synthesis, Natural Products and Material science

Areas Of Interest

Organic Synthesis, Total synthesis of Natural Products, Peptides and Peptidomimetics, Nano Science

Qualification

MSc, PhD, Postdoc.,

Teaching Experience

15 Years 

Awards & Recognition

CSIR-Research Associateship, CSIR, New Delhi, India

Linkedin

Vidwan ID/Profile URL

https://vidwan.inflibnet.ac.in/profile/229860

Scopus ID/Google Scholar ID

http://www.scopus.com/authid/detail.url?authorId=24335776900/ http://scholar.google.co.in/citations?user=nU3uflAAAAAJ

Funded Project (amount sanctioned)

Name of the Principal Investigator/ Co-Investigator (if applicable)

Name of the Funding agency

Type (Government/Non-Government)

Department

Year of Award

Funds provided (INR in lakhs)

Year Of Sanction

Status

1

DST-WOS-A

Govt

Chemical Sciences

2022

22

2022

ongoing

2

REVA

Non-Government

SEED Grant

2021

6

2022

ongoing

PhDs Guided/PhDs Guiding

3

Publications In Refereed Journals

Key Publications (Only Q1 & Q2 rated)

1. Ultrasound accelerated conversion of Nα-urethane protected peptide esters to their thio-peptides using P2S5, V. V. Sureshbabu, G. Nagendra, and R. Venkataramanarao, Ultra-sonics Sonochemistry 15 (2008) 927–929. (Q1, SJR 2018, 1.56)

2. Chiral N-Fmoc-β-Amino Alkyl Isonitriles Derived from Amino Acids: First Synthesis and Application in 1-Substituted Tetrazole Synthesis, V. V. Sureshbabu, N. Narendra and G. Nagendra, J. Org. Chem. 74 (2009)153–157. (Q1, SJR 2018, 1.61)

3. A facile synthesis of N-Z/Boc-protected 1,3,4-oxadiazole based peptidomimetics employ-ing peptidyl thiosemicarbazides, R. S. Lamani, G. Nagendra and V. V. Sureshbabu, Tet-rahedron Lett. 51 (2010) 4705-4709.  (Q2, SJR 2018, 0.62)

4. A convenient synthesis of 1,3,4-thiadiazole and 1,3,4-oxadiazole based peptidomimetics employing diacylhydrazines derived from amino acids, G. Nagendra, Ravi S. Lamani, N. Narendra and, V. V. Sureshbabu, Tetrahedron Lett. 51 (2010) 6338-6341. (Q2, SJR 2018, 0.62)

5. Isoselenocyanates derived from Boc/Z-amino acids: synthesis, isolation, characterization, and application to the efficient synthesis of unsymmetrical selenoureas and selenoureido-peptidomimetics, G. Chennakrishnareddy, G. Nagendra, H. P. Hemantha, U. Das, T. N. Guru Row, V. V. Sureshbabu, Tetrahedron 66 (2010) 6718-6724. (Q2, SJR 2018, 0.71)

6. A facile one-pot synthesis of Nα-Z/Boc-protected S-linked 1,3,4-oxadiazole tethered pep-tidomimetics, V. V Sureshbabu, B. Vasantha and G. Nagendra, Tetrahedron Lett. 53 (2012) 1332-1336. (Q2, SJR 2018, 0.62)

7. Chiral Nβ-Fmoc-amino alkyl isonitriles in Ugi-4CR: an assembly of novel 1,1′-iminodicarboxylated peptidomimetics, N. Narendra, T. M. Vishwanatha, G. Nagendra and V. V. Sureshbabu, Tetrahedron 68 (2012) 1992-2000. (Q2, SJR 2018, 0.71)

8. Synthesis of N-urethane protected α-aminoalkyl-α′-cyanomethyl ketones: An application to the synthesis of 5-amino-3-substituted-1H-pyrazole tethered peptidomimetics, M. K.  Sharnabai, G. Nagendra and V. V. Sureshbabu, Synlett (2012) 1913-1918. (Q1, SJR 2018, 0.86)

9. An expedient route for the reduction of carboxylic acids to alcohols employing 1- pro-panephosphonic acid cyclic anhydride as acid activator, G. Nagendra, C. Madhu, T. M. Vishwanatha and V. V. Sureshbabu, Tetrahedron Lett. 53 (2012) 5059-5063. (Q2, SJR 2018, 0.62)

10. Efficient synthesis of N-protected amino/peptide Weinreb amides from T3P and DBU, K. M. Sharnabai, G. Nagendra, T. M. Vishwanatha, V. V. Sureshbabu, Tetrahedron Lett. 54 (2012) 478-482. (Q2, SJR 2018, 0.62)

11. Observation of a reversible isomorphous phase transtion and an interplay of “σ-hole” and “π-hole” in  Fmoc-Leu-[CH2-NCS], R. Pal, G. Nagendra, M. S. S. Reddy,  V. V. Sureshbabu, T. N. Guru Row,  Chem. Commun. 51 (2015) 933-936. (Q1, SJR 2018, 2.18)

12. A facile synthesis of 1,5-disubstituted tetrazole peptidomimetics by desulfurization/ elec-trocyclization of thiopeptides, Girish Prabhu, G. Nagendra, R. N. Sagar,  R. Pal, T. N. Guru Row, V. V. Sureshbabu,  Asian J. Org. Chem. 5, (2016) 127–137. (Q1, SJR 2018, 0.86)

13. Carbonyl-Assisted Reverse Regioselective Cascade Annulation of 2-Acetylenic Ketones Triggered by Ru-Catalyzed C–H Activation, G. Krishna Kumar,    K. Shivakrishna, G. Nagendra,  N. Jagadeesh babu and Ch. Rambabu, Chem. Sci. 7 (2016) 4748-4753. (Q1, SJR 2018, 3.9)

14. Molecular‐Iodine‐Mediated, Efficient One‐Pot Synthesis of 2‐Iminohydantoins and 2‐Amino‐1H‐imidazol‐4(5H)‐ones by Cyclodeselenization of Selenourea‐Tethered Amides /Peptides, Girish Prabhu, L. Santhosh, G. Nagendra, V. Panduranga, V .V.   Sureshba-bu,  ChemistrySelect 2 (2017) 1202-1206. (Q2, SJR 2018, 0.45)

Other Publications 

1. Synthesis of urea tethered glycosylated amino acids and glycopeptides mediated by DPPA employing Nα-Fmoc-Asp/Glu-5-oxazolidinones, G. Nagendra, H. P. Hemantha, and V. V. Sureshbabu, Indian J. Chem. 48B (2009) 397-407. (Q3, SJR 2018, 0.16)

2. Synthesis of Boc-amino tetrazoles derived from α-amino acids, V. V. Sureshbabu, Shankar A. Naik, and G. Nagendra, Synth. Commun. 39 (2009) 395-406. (Q3, SJR 2018, 0.36).

3. Total synthesis of Cyclosporin O: Exploring the utility of Bsmoc-NMe-amino acid fluorides and KOAt, V. V. Sureshbabu, S. J. Tantry, G. Chennakrishnareddy, and G. Nagendra, Protein Pep. Lett. 16 (2009) 312-319. (Q3, SJR 2018, 0.37).

4. Synthesis of 5-oxo-1-substituted tetrazoles derived from amino acids, G. Nagendra, N, Narendra and V. V. Sureshbabu, Indian J. Chem. 51B (2012) 486-492. (Q3, SJR 2018, 0.16)

5. Capsicum annuum Fruit Extract: A novel reducing agent for the green synthesis of ZnOnanoparticles and their multifunctional applications, H. S. Lalithamba, M. Raghavendra, K. Uma, K. V. Yatish, D. Mousumi, G. Nagendra, Acta. Chim. Slov. 65, (2018) 354-364. (Q3, SJR 2018, 0.27)

6. Synthesis of Terminal Thiazoles from N-Protected Amino Acids and a Study of Their Antibacterial Activities, H. S. Lalithamba, K. Uma, T. S. Gowthami, G. Nagendra, Organic Preparations and Procedures International, (2019) in press, (Q3, SJR 2018, 0.38)

Research Summary

Dr. Nagendra has been working on the design and synthesis of some novel peptidomimetics and related intermediates. His expertise led to the insertion of thioamide linkage 1,3,4-oxadiazole, 1,3,4-thiadiazole, Triazole, Tetrazole, Urea, Thiourea, Selenourea, glycosylated amides etc into the peptide backbone. He was involved in the total synthesis of Cyclosporin-O an immunosuppressive drug and also design of Ugi-MCR reactions. He successfully completed the synthesis of therapeutic analogues for lobeline and 241D towards tobacco cessation and their evaluation, synthesis of new anti cancer agents to inhibit EGFR and AKT.

PhD Guiding: Three

  • Mrs. Dalli Kumari
  • Mr. Gandodi Shaik Saleem
  • Mr. Trimurthulu Sadanala

International Visits

  • Germany
  • Belgium
  • Netherlands
  • Bahrain
  • France

UG / PG Projects

20 

Research Publication

1

Research Project

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