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Yadagiri Dongari
Assistant Professor
yadagiri.dongari[at]cy.iitr.ac.in
+91-133228-5817
https://yadagiridongari.wixsite.com/theyadagirigroup
Research Interests

Biosketch
Educational Details
Professional Background

Research
Projects
Publications
Patents
Books
Collaborations

Honours and Awards
Honors
Memberships

Teaching Engagements
Teaching Engagements

Students
Supervisions
Associate Scholars

Miscellaneous
Events
Visits
Administrative Positions
Miscellaneous
Research Interests
Organic Synthesis & Catalysis, Novel Metallo-Carbene Chemistry, Transition Metal-Catalyzed Site-Selective C-H Functionalization, Visible-Light Induced Transformations
BioSketch
Educational Details
Osmania University, Hyderabad
2008
B.Sc, Mathematics, Physics, Chemistry
Kakatiya University, Warangal
2010
M.Sc, Chemistry
Indian Institute of Technology Madras
2016
Ph.D, Organic Chemistry
Research
Projects
TOPIC START DATE FIELD DESCRIPTION FINANCIAL OUTLAY FUNDING AGENCY OTHER OFFICERS
Metallocarbenes 26 Dec 2022 Organic Synthesis and Catalysis 5786000 SERB-CRG
Functionalization of C-H bonds 22 Oct 2021 Organic Synthesis and Catalysis 2000000 SRIC, IIT Roorkee
Coopertaive catalysis 03 Aug 2021 Organic Synthesis and Catalysis 3500000 DST Inspire




Publications

        

16. Reactivity of Quinone Methides with Carbenes  Generated from α-Diazocarbonyl Compounds and Related  Compounds. Happy, S.; Junaid, M.; Yadagiri, D. Chem. Commun. 202359, 29. †(These authors contributed equally to this work).

15. Catalytic Functionalization of Metallocarbenes Derived from α-Diazocarbonyl Compounds and Their Precursors. Yadagiri, D.; Anbarasan, P. Chem. Rec. 202121, 3872.

14. Denitrogenative Transformations of Pyridotriazoles and Related Compounds: Synthesis of N-Containing Heterocyclic Compounds and Beyond. Yadagiri, D.; Rivas, M.; Gevorgyan, V. J. Org. Chem. 2020, 85, 11030.

13. Light-Induced Metal-Free Transformations of Pyridotriazoles. Zhang, Z.; Yadagiri, D.; Gevorgyan, V. Chem. Sci. 2019, 10, 8399. (These authors contributed equally to this work)

12. Transition Metal- and Light-Free Directed Amination of Remote Unactivated C(sp3)-H Bonds of Alcohols. Kurandina, D.; Yadagiri, D.; Rivas, M.; Kavun, A.; Chuentragool, P.; Hayama, K.; Gevorgyan, V. J. Am. Chem. Soc. 2019, 141,8104.  (These authors contributed equally to this work)

11. Aliphatic Radical Relay Heck Reaction at Unactivated C(sp3)-H Sites of Alcohols. Chuentragool, P.; Yadagiri, D.; Morita, T.; Sarkar, S.; Parasram, M.; Wang, Y.; Gevorgyan, V. Angew. Chem. Int. Ed. 2019, 58, 1794. (These authors contributed equally to this work) This work was highlighted in Synfacts ( 2019, 15, 271).

10. Micelle-enabled Clean and Selective Sulfonylation of Polyfluoroarenes in Water under Mild Conditions. Smith, J. D.; Ansari, T. N.; Andersson, M. P.; Yadagiri, D.; Ibrahim, F.; Liang, S.; Hammond, G. B.; Gallou, F.; Handa. S. Green. Chem. 2018, 20, 1784.

9. Rhodium-Catalyzed Synthesis of Benzopyrans via Transannulation of N-Sulfonyl-1,2,3-triazoles with 2-Hydroxybenzylalcohols. Yadagiri, D.; Chaitanya, M.; Reddy, A. C. S.; Anbarasan, P. Org. Lett. 2018, 20,  3762.

8. Rhodium-Catalyzed Diastereoselective Synthesis of 2,2,3,3-Tetrasubstituted Indolines from N-sulfonyl-1,2,3-Triazoles and ortho-Vinyl Anilines. Yadagiri, D.; Reddy, A. C. S.; Anbarasan, P. Chem. Sci. 2016, 7, 5934. This work was highlighted in Synfacts (2016, 12, 823).

7. One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides. Rajasekar, S.; Yadagiri, D.; Anbarasan, P. Chem. Eur. J. 2015, 21, 17079.

6. An Iodine(III) Mediated Oxidative Rearrangement of Enamines: Efficient Synthesis of α-Aminoketones. Yadagiri, D.; Anbarasan, P. Chem. Commun. 2015, 51, 14203.

5. Tandem 1,2-Sulfur Migration and (Aza)- Diels-Alder Reaction of β- Thio-α-Diazoimines: Rhodium Catalyzed Synthesis of (Fused)- Polyhydropyridines, and Cyclohexanes. Yadagiri, D.; Anbarasan, P. Chem. Sci. 2015, 6, 5847.

4. Recent Advances in Transition Metal Catalyzed Denitrogenative Transformation of 1,2,3-Triazoles and Related Compounds. Anbarasan, P.; Yadagiri, D.; Rajasekar, S. Synthesis 2014, 46, 3004. (Invited review).

3. Rhodium-Catalyzed Direct Arylation of α-Diazoimines. Yadagiri, D.; Anbarasan, P. Org. Lett. 2014, 16, 2510.

2. Rhodium-Catalyzed Cyanation of Chelation Assisted C-H Bonds. Chaitanya, M.; Yadagiri, D.; Anbarasan, P. Org. Lett. 2013, 15, 4960.

1. Rhodium-Catalyzed Denitrogenative [2,3]-Sigmatropic Rearrangement: An Efficient Entry to Sulfur Containing Quaternary Center. Yadagiri, D.; Anbarasan, P. Chem. Eur. J. 2013, 19, 15115.

Honors And Awards
Honors
Department of Science and Technology, Government of India
2021
DST-INSPIRE faculty award
University of Texas at Dallas, USA
2020
Postdoctoral Fellowship
University of Illinois at Chicago, USA
2017
Postdoctoral Fellowship
Eli Lilly and Company
2016
Eli Lilly and Company Asia Outstanding Thesis Award
Indian Institute of Technology Madras
2016
Prof. C. N. Pillai Prize for Best Ph. D. Thesis Award of the Year in the Department of Chemistry
Indian Institute of Technology Madras
2015
Institute Pre-Doctoral Fellowship Award
Indian Institute of Technology Madras
2013
Best Oral Presentation Award in CiHS-2013
Indian Institute of Technology Madras
2012
Junior Research Fellowship (JRF) and Senior Research Fellowship (SRF)
Teaching Engagements
Teaching Engagements
Advanced Organic Chemistry ( CYN-903 )
Autumn
Laboratory 1 ( CYN-311 )
Autumn
Organic Chemistry VI ( CYN-526 )
Spring
Laboratory II ( CYN-312 )
Spring
Organic and Inorganic Chemistry ( CYN-002 )
Spring
Miscellaneous
Administrative Positions
Assistant Professor
03 May 2021 - Present
Indian Institute of Technology Roorkee
Senior Research Investigator
01 Dec 2020 - 30 Apr 2021
Biocon Bristol-Myers Squibb Research & Development Center
Postdoctoral Research Associate
31 May 2019 - 31 Aug 2020
University of Texas at Dallas
Postdoctoral Research Associate
21 Jul 2017 - 31 May 2019
University of Illinois at Chicago
Postdoctoral Research Associate
13 Feb 2017 - 20 Jul 2017
University of Louisville
Research Associate
01 Apr 2016 - 12 Feb 2017
Indian Institute of Technology Madras