PUBLICATIONS
From IIT Roorkee
20. Light–Induced Reactivity of Nucleophilic Siloxycarbene with Heterocumulenes: Synthesis of ⍺-Ketoamides, Hydantoins, Oxoacetamidines, and Amides.
Saleem, M.; Abhishek, P.; Yadagiri, D. Org. Lett. 2024, 26, 10291.
19. Light–Driven Intramolecular Cyclopropanation of Alkene-Tethered N-Tosylhydrazones; Synthesis of Fused-Cyclopropane 𝜸-Lactones.
Yamini, P.; Babbar, A.; Yadagiri, D. Org. Lett. 2024, 26, 6035.
18. Visible-Light Induced Siloxycarbene Addition to N=N of Azodicarboxylates: Synthesis of Acyl Hydrazides from Acylsilanes.
Saleem, M.; Ratwan, A.; Yamini, P.; Yadagiri, D. Org. Lett. 2024, 26, 2039. Highlighted on Organic Chemistry Portal. Check it here: https://www.organic-chemistry.org/abstracts/lit9/479.shtm
17. Light-Induced Arylation (Alkylation) of N-Sulfonylhydrazones with Boronic Acids.
Junaid, M.; Happy, S.; Yadagiri, D. Chem. Commun. 2024, 60, 2796.
16. Rhodium-Catalyzed [4+2]-Annulation of o-Acylanilines with N-Sulfonyl-1,2,3-Triazoles: Synthesis of 3-Aminoquinolines.
Rupa, K.; Yadagiri, D.; Anbarasan, P. J. Org. Chem. 2023, 88, 9077.
15. Synthesis of Dihydro-3,1-benzoxazine Derivatives from 1,3-Amino Alcohols and N-Sulfonyl-1,2,3-triazole.
Rupa, K.; Yadagiri, D.; Bagavathi, R.; Anbarasan, P. Org. Lett. 2023, 25, 3375.
Prior to IIT Roorkee
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.