5

14. Touney, E. E.*; Cooper, R. E.*; Bredenkamp, S. E.; George, D. T.; Pronin, S. V. Catalytic radical-polar crossover Ritter reaction. ChemRxiv. Preprint. https://doi.org/10.26434/chemrxiv.14450580.v1

* equally-contributing authors

13. Foy, N. J.; Pronin, S. V. Synthesis of pleuromutilin. J. Am. Chem. Soc. 2022, 144, 10174.

12. Thomas, W. P.; Pronin, S. V. A concise enantioselective approach to quassinoids. J. Am. Chem. Soc. 2022, 144, 118.

11. Schatz, D. J.; Kuenstner, E. J.; George, D. T.; Pronin, S. V. Synthesis of rearranged indole diterpenes of the paxilline type. Nat. Prod. Rep. 2022, 39, 946.

10. Thomas, W. P.; Pronin, S. V. New methods and strategies in the synthesis of natural products. Acc. Chem. Res. 2021, 54, 1347.

9. Discolo, C. A.*; Touney, E. E.*; Pronin, S. V. Catalytic asymmetric radical-polar crossover hydroalkoxylation. J. Am. Chem. Soc. 2019, 141, 17527.

* equally-contributing authors

8. Thomas, W. P.; Schatz, D. J.; George, D. T.; Pronin, S. V. A radical-polar crossover annulation to access terpenoid motifs. J. Am. Chem. Soc. 2019, 141, 12246.

7. Schatz, D. J.; Li, W.; Pronin, S. V. Catalytic enantioselective conjugate addition en route to paxilline indoloterpenoids. Tetrahedron 2019, 75, 3361. [invited submission to a special issue in honor of Ryan Shenvi]

6. Touney, E. E.; Foy, N. J.; Pronin, S. V. Catalytic radical-polar crossover reactions of allylic alcohols. J. Am. Chem. Soc. 2018, 140, 16982.

5. Godfrey, N. A.*; Schatz, D. J.*; Pronin, S. V. Twelve-step asymmetric synthesis of (–)-nodulisporic acid C. J. Am. Chem. Soc. 2018, 140, 12770.

* equally-contributing authors

4. Holmbo, S. D.; Pronin, S. V. A concise approach to anthraquinone-xanthone heterodimers. J. Am. Chem. Soc. 2018, 140, 5065.

3.   George, D. T.; Kuenstner, E. J.; Pronin, S. V. Synthesis of emindole SB. Synlett 2017, 28, 12. [invited account]

2.   Holmbo, S. D.*; Godfrey, N. A.*; Hirner, J. J.; Pronin, S. V. A catalytic intermolecular formal ene reaction between ketone-derived silyl enol ethers and alkynes. J. Am. Chem. Soc. 2016, 138, 12316.

* equally-contributing authors

alkenylation

1.   George, D. T.; Kuenstner, E. J.; Pronin, S. V. A concise approach to paxilline indole diterpenes. J. Am. Chem. Soc. 2015, 137, 15410.

Screen Shot 2015-11-23 at 12.30.17 PM

Before UCIrvine

8.   Lu, H.-H.*; Pronin, S. V.*; Antonova-Koch, Y.; Meister, S.; Winzeler, E. A.; Shenvi, R. A. Synthesis of (+)-7,20-diisocyanoadociane and liver-stage antiplasmodial activity of the isocyanoterpene class. J. Am. Chem. Soc. 2016, 138, 7268.

* equally-contributing authors

7.   Pronin, S. V.; Reiher, C. A.; Shenvi, R. A. Stereoinversion of tertiary alcohols to tert-alkyl isonitriles and amines. Nature, 2013, 501, 195.

6.   Pronin, S. V.; Shenvi, R. A. Synthesis of a potent antimalarial amphilectene. J. Am. Chem. Soc. 2012, 134, 19604.

5.   Pronin, S. V.; Shenvi, R. A. Synthesis of highly strained terpenes by nonstop tail-to-head polycyclization Nat. Chem. 2012, 4, 915.

  • Highlighted by Matteo Zanda in SYNFORM 2013, A19.

4.   Pronin, S. V.; Tabor, M. G.; Jansen, D. J.; Shenvi, R. A. Stereoselective hydroamination transform to access polysubstituted indolizidines. J. Am. Chem. Soc.134, 2012.

3.   Pronin, S. V.; Martinez, A.; Kuznedelov, K.; Severinov, K. V.; Shuman, H. A.; Kozmin, S. A. Chemical synthesis enables biochemical and antibacterial evaluation of streptolydigin antibiotics. J. Am. Chem. Soc. 2011133, 12172.

2.   Pronin, S. V.; Kozmin, S. A. Synthesis of streptolydigin, a potent bacterial RNA polymerase inhibitor. J. Am. Chem. Soc. 2010, 132, 14394.

1.   Nenajdenko, V. G.; Pronin, S. V.; Balenkova, E. S. Synthesis of aminoalkyl pyrazoles and isoxazoles from cyclic β-(trifluoroacetyl)examines. Russ. Chem. Bull., Int. Ed. 2007, 56, 336.