Year |
Citation |
Score |
2023 |
Pinter EN, Sheldon ZS, Modak A, Cook SP. Fluorosulfonamide-Directed Heteroarylation of Aliphatic C(sp)-H Bonds. The Journal of Organic Chemistry. PMID 36912807 DOI: 10.1021/acs.joc.2c02461 |
0.753 |
|
2022 |
Lee H, He T, Cook SP. Iron-Catalyzed, Directed Benzylic Borylation. Organic Letters. PMID 36550075 DOI: 10.1021/acs.orglett.2c02864 |
0.485 |
|
2022 |
Liu ZY, Cook SP. Directed Ni-Catalyzed Reductive Arylation of Aliphatic C-H Bonds. Organic Letters. 24: 3313-3318. PMID 35499249 DOI: 10.1021/acs.orglett.2c00447 |
0.375 |
|
2021 |
He J, Nguyen TN, Guo S, Cook SP. Csp-H Trifluoromethylation of Unactivated Aliphatic Systems. Organic Letters. PMID 33443442 DOI: 10.1021/acs.orglett.0c03891 |
0.403 |
|
2021 |
Liu ZY, Cook SP. Interrupting the Barton-McCombie Reaction: Aqueous Deoxygenative Trifluoromethylation of -Alkyl Thiocarbonates. Organic Letters. PMID 33443440 DOI: 10.1021/acs.orglett.0c04039 |
0.367 |
|
2020 |
Modak A, Nett AJ, Swift EC, Haibach MC, Chan VS, Franczyk TS, Shekhar S, Cook SP. Cu-Catalyzed C-N Coupling with Sterically Hindered Partners. Acs Catalysis. 10: 10495-10499. PMID 37063689 DOI: 10.1021/acscatal.0c02965 |
0.737 |
|
2020 |
Pinter EN, Bingham JE, AbuSalim DI, Cook SP. N-Directed fluorination of unactivated Csp3–H bonds Chemical Science. 11: 1102-1106. DOI: 10.1039/C9Sc04055B |
0.401 |
|
2020 |
Modak A, Nett AJ, Swift EC, Haibach MC, Chan VS, Franczyk TS, Shekhar S, Cook SP. Cu-Catalyzed C–N Coupling with Sterically Hindered Partners Acs Catalysis. 10: 10495-10499. DOI: 10.1021/Acscatal.0C02965 |
0.726 |
|
2019 |
Pinter EN, Bingham JE, AbuSalim DI, Cook SP. N-Directed fluorination of unactivated Csp-H bonds. Chemical Science. 11: 1102-1106. PMID 34084366 DOI: 10.1039/c9sc04055b |
0.343 |
|
2019 |
Modak A, Pinter EN, Cook SP. Copper-Catalyzed, N-Directed Csp-H Trifluoromethylthiolation (-SCF) and Trifluoromethylselenation (-SeCF). Journal of the American Chemical Society. PMID 31697070 DOI: 10.1021/Jacs.9B10316 |
0.757 |
|
2019 |
Groendyke BJ, Modak A, Cook SP. Fenton-Inspired C-H Functionalization: Peroxide-Directed C-H Thioetherification. The Journal of Organic Chemistry. PMID 31524395 DOI: 10.1021/Acs.Joc.9B01979 |
0.751 |
|
2019 |
Marcyk PT, Cook SP. Synthesis of Tetrahydroisoquinolines Through an Iron-Catalyzed Cascade: Tandem Alcohol Substitution and Hydroamination. Organic Letters. PMID 31418575 DOI: 10.1021/Acs.Orglett.9B02353 |
0.429 |
|
2019 |
Guo S, AbuSalim D, Cook S. 1,2-(Bis)trifluoromethylation of Alkynes: A One-Step Reaction to Install an Underutilized Functional Group. Angewandte Chemie (International Ed. in English). PMID 31206968 DOI: 10.1002/Anie.201905247 |
0.43 |
|
2019 |
Sahota N, AbuSalim DI, Wang ML, Brown CJ, Zhang Z, El-Baba TJ, Cook SP, Clemmer DE. A microdroplet-accelerated Biginelli reaction: mechanisms and separation of isomers using IMS-MS. Chemical Science. 10: 4822-4827. PMID 31160956 DOI: 10.1039/C9Sc00704K |
0.409 |
|
2019 |
Marcyk PT, Cook SP. Iron-Catalyzed Hydroamination and Hydroetherification of Unactivated Alkenes. Organic Letters. 21: 1547-1550. PMID 30789740 DOI: 10.1021/Acs.Orglett.9B00427 |
0.43 |
|
2018 |
Cook S, Marcyk PT, Jefferies LR, AbuSalim DI, Pink M, Baik MH. Stereoinversion of Unactivated Alcohols by Tethered Sulfonamides. Angewandte Chemie (International Ed. in English). PMID 30536739 DOI: 10.1002/Anie.201812894 |
0.31 |
|
2018 |
Guo S, AbuSalim DI, Cook SP. Aqueous Benzylic C-H Trifluoromethylation for Late-Stage Functionalization. Journal of the American Chemical Society. PMID 30247886 DOI: 10.1021/Jacs.8B08547 |
0.407 |
|
2018 |
Rosas Vargas D, Cook SP. Palladium nanoparticles: Chemoselective control for reductive Heck with aryl triflates and 2,3-dihydrofuran Tetrahedron. 74: 3314-3317. DOI: 10.1016/J.Tet.2018.04.052 |
0.497 |
|
2016 |
Groendyke BJ, AbuSalim DI, Cook SP. Iron-Catalyzed, Fluoroamide-Directed C-H Fluorination. Journal of the American Chemical Society. PMID 27676449 DOI: 10.1021/Jacs.6B08171 |
0.527 |
|
2016 |
Atack TC, Cook SP. Manganese-Catalyzed Borylation of Unactivated Alkyl Chlorides. Journal of the American Chemical Society. 138: 6139-42. PMID 27158838 DOI: 10.1021/Jacs.6B03157 |
0.499 |
|
2014 |
Agrawal T, Cook SP. Iron-catalyzed coupling of aryl sulfamates and aryl/vinyl tosylates with aryl Grignards. Organic Letters. 16: 5080-3. PMID 25230097 DOI: 10.1021/Ol5024344 |
0.549 |
|
2014 |
Monks BM, Fruchey ER, Cook SP. Iron-catalyzed C(sp²)-H alkylation of carboxamides with primary electrophiles. Angewandte Chemie (International Ed. in English). 53: 11065-9. PMID 25088928 DOI: 10.1002/Anie.201406594 |
0.746 |
|
2014 |
Fruchey ER, Monks BM, Cook SP. A unified strategy for iron-catalyzed ortho-alkylation of carboxamides. Journal of the American Chemical Society. 136: 13130-3. PMID 25083946 DOI: 10.1021/Ja506823U |
0.783 |
|
2014 |
Atack TC, Lecker RM, Cook SP. Iron-catalyzed borylation of alkyl electrophiles. Journal of the American Chemical Society. 136: 9521-3. PMID 24955892 DOI: 10.1021/Ja505199U |
0.484 |
|
2014 |
Jefferies LR, Cook SP. Iron-catalyzed arene alkylation reactions with unactivated secondary alcohols. Organic Letters. 16: 2026-9. PMID 24666277 DOI: 10.1021/Ol500606D |
0.458 |
|
2014 |
Jefferies LR, Weber SR, Cook SP. Iron-catalyzed C-N bond formation via the Beckmann rearrangement Synlett. 25. DOI: 10.1055/S-0034-1379540 |
0.513 |
|
2014 |
Jefferies LR, Cook SP. Alcohols as electrophiles: Iron-catalyzed Ritter reaction and alcohol addition to alkynes Tetrahedron. 70: 4204-4207. DOI: 10.1016/J.Tet.2014.03.072 |
0.48 |
|
2013 |
Monks BM, Cook SP. Palladium-catalyzed intramolecular iodine-transfer reactions in the presence of β-hydrogen atoms. Angewandte Chemie (International Ed. in English). 52: 14214-8. PMID 24254862 DOI: 10.1002/Anie.201308534 |
0.747 |
|
2013 |
Fruchey ER, Monks BM, Patterson AM, Cook SP. Palladium-catalyzed alkyne insertion/reduction route to trisubstituted olefins. Organic Letters. 15: 4362-5. PMID 23957428 DOI: 10.1021/Ol4018694 |
0.783 |
|
2013 |
Cook SP. The quest for affordable artemisinin. Future Medicinal Chemistry. 5: 233-6. PMID 23464512 DOI: 10.4155/Fmc.13.1 |
0.406 |
|
2013 |
DeLuca RJ, Edwards JL, Steffens LD, Michel BW, Qiao X, Zhu C, Cook SP, Sigman MS. Wacker-type oxidation of internal alkenes using Pd(Quinox) and TBHP. The Journal of Organic Chemistry. 78: 1682-6. PMID 23363387 DOI: 10.1021/Jo302638V |
0.572 |
|
2013 |
Agrawal T, Cook SP. Iron-catalyzed cross-coupling reactions of alkyl Grignards with aryl sulfamates and tosylates. Organic Letters. 15: 96-9. PMID 23244161 DOI: 10.1021/Ol303130J |
0.54 |
|
2012 |
Monks BM, Cook SP. Palladium-catalyzed alkyne insertion/Suzuki reaction of alkyl iodides. Journal of the American Chemical Society. 134: 15297-300. PMID 22958064 DOI: 10.1021/Ja307761F |
0.787 |
|
2012 |
Zhu C, Cook SP. A concise synthesis of (+)-artemisinin. Journal of the American Chemical Society. 134: 13577-9. PMID 22866604 DOI: 10.1021/Ja3061479 |
0.346 |
|
2012 |
Gao P, Cook SP. A reductive-Heck approach to the hydroazulene ring system: a formal synthesis of the englerins. Organic Letters. 14: 3340-3. PMID 22679931 DOI: 10.1021/Ol3013167 |
0.516 |
|
2012 |
Jarugumilli GK, Zhu C, Cook SP. Re-evaluating the nucleophilicity of zinc enolates in alkylation reactions European Journal of Organic Chemistry. 1712-1715. DOI: 10.1002/Ejoc.201200067 |
0.485 |
|
2011 |
Jarugumilli GK, Cook SP. A simple, nontoxic iron system for the allylation of zinc enolates. Organic Letters. 13: 1904-7. PMID 21391714 DOI: 10.1021/Ol200059U |
0.471 |
|
2008 |
Polara A, Cook SP, Danishefsky SJ. Multiple chirality transfers in the enantioselective synthesis of 11-O-debenzoyltashironin. Chiroptical analysis of the key cascade. Tetrahedron Letters. 49: 5906-5908. PMID 19812682 DOI: 10.1016/J.Tetlet.2008.07.139 |
0.442 |
|
2008 |
Polara A, Cook SP, Danishefsky SJ. Multiple chirality transfers in the enantioselective synthesis of 11-O-debenzoyltashironin. Chiroptical analysis of the key cascade. Tetrahedron Letters. 49: 5906-5908. PMID 19812682 DOI: 10.1016/J.Tetlet.2008.07.139 |
0.442 |
|
2006 |
Cook SP, Polara A, Danishefsky SJ. The total synthesis of (+/-)-11-O-debenzoyltashironin. Journal of the American Chemical Society. 128: 16440-1. PMID 17177359 DOI: 10.1021/Ja0670254 |
0.409 |
|
2006 |
Cook SP, Polara A, Danishefsky SJ. The total synthesis of (+/-)-11-O-debenzoyltashironin. Journal of the American Chemical Society. 128: 16440-1. PMID 17177359 DOI: 10.1021/Ja0670254 |
0.409 |
|
2006 |
Cook SP, Danishefsky SJ. An interesting issue of Diels-Alder selectivity discovered en route to 11-O-debenzoyltashironin. Organic Letters. 8: 5693-5. PMID 17134249 DOI: 10.1021/Ol062067I |
0.541 |
|
2005 |
Cook SP, Christoph G, Danishefsky SJ. En route to the total synthesis of tashironin: On the exercise of stereochemical control by a methyl group in mediating remote cyclization reactions Tetrahedron Letters. 46: 843-847. DOI: 10.1016/J.Tetlet.2004.11.148 |
0.58 |
|
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