Independent Publications

20. Groendyke, B.; AbuSalim, D.; Cook, S. P. “Iron-Catalyzed, Fluoroamide-Directed C–H Fluorination,” J. Am. Chem. Soc., 2016, 138, 12771–12774. [10.1021/jacs.6b08171]
Highlighted in:
C&E News
2016, 94, 40, October 10th. [link]

19. Atack, T. C. and Cook, S. P. “Manganese-Catalyzed Borylation of Unactivated Chlorides,” J. Am. Chem. Soc., 2016, 138, 6139–6142. [10.1021/jacs.6b03157]
Highlighted in:
ChemInform 2016, 47. [10.1002/chin.201646196]

18. Jefferies, L. R.; Weber, S. R.; Cook, S. P. “Iron-Catalyzed C–N Bond Formation via the Beckmann Rearrangement,” Synlett, 2015, 26, 331–334. [10.1055/s-0034-1379540] Invited Paper for the "Catalysis with Sustainable Metals" Special Issue.


17. Agrawal, T.; Cook, S. P. "Iron-Catalyzed Coupling of Aryl Sulfamates and Aryl/Vinyl Tosylates with Aryl Grignards," Org. Lett., 2014 16, 5080–5083 . [10.1021/ol024344]

16. Fruchey, E. R.; Monks, B. M.; Cook, S. P. "A Unified Strategy for Iron-Catalyzed ortho-Alkylation of Carboxamides," J. Am. Chem. Soc., 2014,136, 13130–13133. [10.1021/ja506823u]

15. Monks, B. M.; Fruchey, E. R.; Cook, S. P. "Iron-Catalyzed C(sp2)–H Alkylation of Carboxamides with Primary Electrophiles,"Angew. Chem. Int. Ed., 2014, 53, 11065–11069. [anie.201406594] Selected as "Hot Paper" by Angew. Chem.

14. Atack, T. C.; Lecker, R. M.; Cook, S. P. "Iron-Catalyzed Borylation of Alkyl Electrophiles," J. Am. Chem. Soc., 2014, 136, 9521–9523. [10.1021/ja505199u]
Highlighted in:
Org. Proc. Res. Dev. 2014, 18, 1047-1082. [10.1021/op500257q]
Synfacts 2014, 10, 1070. [10.1055/s-0034-1379113]
ChemInform 2015, 46, A. [10.1002/chin.201506218]
Org. Chem. Highlights 2015, May 25. [link]

13. Jefferies, L. R.; Cook, S. P. “Alcohols as Electrophiles: Iron-Catalyzed Ritter Reactions and Benzyl Alcohol Additions to Alkynes,” Tetrahedron, 2014, 70, 4204–4207. [10.1016/j.tet.2014.03.072] Invited Paper in honor of Professor Sarah Reisman receiving the Tetrahedron Young Investigator Award.

12. Jefferies, L. R.; Cook, S. P. “Iron-Catalyzed Arene Alkylation Reactions with Unactivated Secondary Alcohols,” Org. Lett., 2014, 16, 2026–2029. [10.1021/ol500606d]
Highlighted in:
Synfacts 2014, 10, 747. [10.1055/s-0033-1339147]
Org. Chem. Highlights 2014, October 13. [link]


11. Cook, S. P. “Artemisinin: A Case Study in the Evolution of Synthetic Strategy,” Synlett, 2014, 25, 751–759. [10.1055/s-0033-1340627] Invited Synpacts review.

10. Monks, B. M.; Cook, S. P. "Palladium-Catalyzed, Intramolecular Iodine-Transfer Reactions in the Presence of β-Hydrogens," Angew. Chem. Int. Ed., 2013, 52, 14214–14218. [anie.201308534]


9. Fruchey, E. R.; Monks, B. M.; Patterson, A. M.; Cook, S. P. "Palladium-Catalyzed Alkyne Insertion/Reduction Route to Trisubstituted Olefins," Org. Lett.201315, 4362–4365. [10.1021/ol4018694]

8. Cook, S. P. "The quest for affordable artemisinin," Future Med. Chem.20135, 233–236. [10.4155/fmc.13.1] Invited editorial.


7. DeLuca, R. J.; Edwards, J. L.; Steffens, L. D.; Michel, B. W.; Qiao, X.; Zhu, C.; Cook, S. P.; Sigman, M. S. "Wacker-Type Oxidation of Internal Alkenes using Pd(Quinox) and TBHP," J. Org. Chem.201378, 1682–1686. [10.1021/jo302638v]


6. Agrawal, T.; Cook, S. P. "Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Sulfamates and Tosylates," Org. Lett., 2013, 15, 96–99. [10.1021/ol303130j]
Highlighted in
Org. Proc. Res. Dev. 201317, 320-329. [10.1021/op400031g]
2013, 9, 422. [10.1055/s-0032-1318378]


5. Monks, B. M.; Cook, S. P. "Palladium-Catalyzed Alkyne Insertion/Suzuki Reaction of Alkyl Iodides," J. Am. Chem. Soc., 2012, 134, 15297–15300. [10.1021/ja3077611f]


4. Zhu, C.; Cook, S. P. "A Concise Synthesis of (+)-Artemisinin," J. Am. Chem. Soc., 2012, 134, 13577–13579. [10.1021/ja3061479]
Highlighted in:
One of 2012's "Most Read" papers in JACS.
C&E News
2012, 90, 28. [link]
JACS Spotlights 2012, 134, 15163–15164. [10.1021/ja3084187]
Nature Chemical Biology 2012, 8, 808. [10.1038/nchembio.1073]
"Synfact of the Month" Synfacts 2012, 11, 1163. [10.1055/s-0032-1317408]
Nature Chemistry 2012, 4, 772. [10.1038/nchem.1473]
"Synthesis: A Constructive Debate" Nature 2012, 492, 188. [10.1038/492188a]
Org. Chem. Highlights 2013, April 15. [link]


3. Gao, P.; Cook, S. P. "A Reductive-Heck Approach to the Hydroazulene Ring System: A Formal Synthesis of the Englerins," Org. Lett., 2012, 14, 3340–3343. [10.1021/ol3013167]


2. Jarugumilli, G. K.; Zhu, C.; Cook, S. P. "Re-Evaluating the Nucleophilicity of Zinc Enolates in Alkylation Reactions," Eur. J. Org. Chem., 2012, 1712–1715. [10.1002/ejoc.201200067]

1. Jarugumilli, G. K.; Cook, S. P. "A Simple, Nontoxic Iron System for the Allylation of Zinc Enolates," Org. Lett., 2011, 13, 1904–1907. [10.1021/ol200059u]
Highlighted in:
Synfacts 2011, 7, 773. [10.1055/s-0030-1260504]


Pre-IU Publications

Polara, A.; Cook, S. P.; Danishefsky, S. J. “Multiple Chirality Transfers in the Enantioselective Synthesis of 11-O-debenzoyltashironin. Chiroptical Analysis of the Key Cascade,” Tetrahedron Lett. 2008, 49, 5906–5908.  

Vincent, F.; Cook, S. P.; Johnson, E. O.; Emmert, D.; Shah, K. “Engineering Unnatural Nucleotide Specificity to Probe G Protein Signaling,” Chem. Biol. 2007, 14, 1007–1018. 
Cook, S. P.; Polara, A.; Danishefsky, S. J. “The Total Synthesis of 11-O-Debenzoyltashironin,” J. Am. Chem. Soc. 2006, 128, 16440–16441. 
Cook, S. P.; Danishefsky, S. J. “An Interesting Issue of Diels-Alder Selectivity Discovered En Route to 11-O-Debenzoyltashironin,” Org. Lett. 2006, 8, 5693–5695. 

Cook, S. P.; Gaul, C.; Danishefsky, S. J. “En Route to the Total Synthesis of Tashironin:  On the Exercise of Stereochemical Control by a Methyl Group in Mediating Remote Cyclization Reactions,” Tetrahedron Lett. 2005, 46, 843–847. 
Miura, M.; Morris, G. M.; Micca, P. L.; Nawrocky, M. M.; Makar, M. M.; Cook, S. P.; Slatkin, D. N. “Synthesis of Copper Octabromotetracarboranylphenylporphyrin for Boron Neutron Capture Therapy and its Toxicity and Biodistribution in Tumour-Bearing Mice,” Br. J. Radiol. 2004, 77, 573–580. 
Cook, S. P.; Galve-Roperh, I.; Martinez del Pozo, A.; Rodriguez-Crespo, I; “Direct Calcium Binding Results in the Activation of Brain Serine Racemase,” J. Biol. Chem. 2002, 277, 27782–27792.