[16] Ping, K.; Kahnert, S. R.; Ley, J. M.; Bhadoria, R.; Starkov, P.* M–N–C materials as heterogeneous catalysts for organic transformations. Submitted [Review]

[15] Alam, M.; Ping, K.; Danilson, M.; Mikli, V.; Käärik, M.; Leis, Aruväli, J.; Paiste, P.; Rähn, M.; Sammelselg, V.; Tammeveski, K.; Kongi, N.;* Starkov, P.* Iron triad metal alloy nanomaterials as trifunctional catalysts in alkaline and acidic media. Submitted. [Article]

[14] Ping, K.; Alam, M.; Kahnert, S. R.; Bhadoria, R.; Mere, A.; Mikli, V.; Käärik, M.; Aruväli, J.; Paiste, P.; Kikas, A.; Kisand, V.; Järving, I.; Leis, J.; Kongi, N.*; Starkov, P.* Multi-purpose chemo- and electrocatalyst material from an amorphous cobalt metal–organic framework. Mater. Adv. 2021, 2, 4009-4015.  DOI:10.1039/D1MA00414J

[13] Kazimova, N.; Ping, K.; Alam, M.; Danilson, M.; Merisalu, K.; Käärik, M.; Mikli, V.; Aruväli, J.; Paiste, P.; Leis, J.; Tammeveski, K.; Starkov, P.;* Kongi, N.* Shungite-derived graphene as a carbon support for bifunctional oxygen electrocatalysts. J. Catal. 2021, 395, 178–187. DOI:10.1016/j.jcat.2021.01.004

[12] Bhadoria, R.; Ping, K.; Lohk, C.; Järving, I.; Starkov, P.* A phenotypic approach to probing cellular outcomes using heterobivalent constructs. Chem. Commun. 2020, 56, 4216–4219.  DOI:10.1039/C9CC09595K

[11] Ping, K.; Braschinsky, A.; Alam, M.; Bhadoria, R.; Mihkli, V.; Mere, A.; Aruväli, J.; Paiste, P.; Vlassov, S.; Kook, M.; Rähn, M.; Sammelselg, K.; Tammeveski, K.; Kongi, N.;* Starkov, P.* Fused hybrid linkers for metal–organic framework-derived bifunctional oxygen electrocatalysts. ACS Appl. Energy Mater. 2020, 3, 152–157. DOI:10.1021/acsaem.9b02039

[10] Ping, K.; Alam, M.; Käärik, M.; Leis, J.; Kongi, N.; Järving, I.; Starkov, P.* Surveying iron–organic framework TAL-1 derived materials in ligandless heterogenous oxidative catalytic transformations of alkylarenes. Synlett 2019, 30, 1536–1540.  DOI:10.1055/s-0037-1611877  [10th EuCheMS-YIW-Invited]

[9]  Kasak, L.; Näks, M.; Eek, P.; Piirsoo, A.; Bhadoria, R.; Starkov, P.; Saarma, M.; Kasvandik, S.; Piirsoo, M.* Characterization of protein kinase ULK3 regulation by phosphorylation and inhibition by small molecule SU6668. Biochemistry 2018, 57, 5456–5465.  DOI:10.1021/acs.biochem.8b00356


[8] Starkov, P.; Moore, J. T.; Duquette, D. C.; Stoltz, B. M.;* Marek, I.* Enantioselective construction of acyclic quaternary carbon stereocenters: Palladium-catalyzed decarboxylative allylic alkylation of fully substituted amide enolates. J. Am. Chem. Soc. 2017, 139, 9615–9620. DOI:10.1021/jacs.7b04086

[7] Lanigan, R. M.; Karaluka, V.; Sabatini, M. T.; Starkov, P.; Badland, M.; Boulton, L. T.; Sheppard, T. D.* Direct amidation of unprotected amino acids using B(OCH2CF3)3. Chem. Commun. 2016, 52, 8846–8849.  DOI:10.1039/c0cc05147b

[6] Starkov, P.; Jamison, T. F.; Marek, I.* Electrophilic amination: The case of nitrenoids. Chem. Eur. J. 2015, 21, 5278–5300. DOI:10.1002/chem.201405779

[5] Lanigan, R.; Starkov, P.; Sheppard, T. D.* Direct synthesis of amides from carboxylic acids and amines using B(OCH2CF3)3. J. Org. Chem. 2013, 78, 4512–4523.  DOI:10.1021/jo400509n

[4] Starkov, P.; Rota, F.; D’Oyley.; Sheppard, T. D.* Catalytic electrophilic halogenation of silyl‐protected and terminal alkynes: Trapping gold (I) acetylides vs. a Brønsted acid‐promoted reaction. Adv. Synth. Catal. 2012, 354, 3217–3224.  DOI:10.1002/adsc.201200491

[3] Starkov, P.; Sheppard. T. D.* Borate esters as convenient reagents for direct amidation of carboxylic acids and transamidation of primary amides. Org. Biomol. Chem. 2011, 9, 1320–1323.  DOI:10.1039/c0ob01069c

[2] Körner, C.; Starkov, P.; Sheppard, T. D.* An alternative approach to aldol reactions: Gold-catalyzed formation of boron enolates from alkynes. J. Am. Chem. Soc. 2010, 132, 5968–5969.  DOI:10.1021/ja102129c

[1] Starkov, P.; Zemskov, I.; Sillard, R.; Tšubrik, O.; Mäeorg, U.* Copper-catalyzed N-arylation of carbamate-protected hydrazones with organobismuthanes. Tetrahedron Lett. 2007, 48, 1155–1157.  DOI:10.1016/j.tetlet.2006.12.071


[TH] Starkov, P. Applications of boronic acids in organic synthesis. PhD thesis, University College London, 2011. Link