| Year |
Citation |
Score |
| 2024 |
Jiao Z, Jaunich KT, Tao T, Gottschall O, Hughes MM, Turlik A, Schuppe A. Unified Approach to Deamination and Deoxygenation Through Isonitrile Hydrodecyanation: A Combined Experimental and Computational Investigation. Angewandte Chemie (International Ed. in English). e202405779. PMID 38619535 DOI: 10.1002/anie.202405779 |
0.564 |
|
| 2023 |
Lyu H, Tugwell TH, Chen Z, Kukier GA, Turlik A, Wu Y, Houk KN, Liu P, Dong G. Modular synthesis of 1,2-azaborines via ring-opening BN-isostere benzannulation. Nature Chemistry. PMID 37783725 DOI: 10.1038/s41557-023-01343-6 |
0.399 |
|
| 2023 |
Alcock E, Mackey P, Turlik A, Bhatt K, Light M, Houk K, McGlacken GP. The Double Aldol-Tishchenko Reaction of Butanone, Cyclobutanone and a 3-Pentanone Derived Sulfinylimine and DFT Calculations of the Stereo-determining Step. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36617506 DOI: 10.1002/chem.202203029 |
0.333 |
|
| 2022 |
Kerkovius JK, Stegner A, Turlik A, Lam PH, Houk KN, Reisman SE. A Pyridine Dearomatization Approach to the Matrine-Type Lupin Alkaloids. Journal of the American Chemical Society. PMID 36006400 DOI: 10.1021/jacs.2c06584 |
0.313 |
|
| 2022 |
Wu X, Turlik A, Luan B, He F, Qu J, Houk KN, Chen Y. Nickel-Catalyzed Enantioselective Reductive Alkyl-Carbamoylation of Internal Alkenes. Angewandte Chemie (International Ed. in English). e202207536. PMID 35818326 DOI: 10.1002/anie.202207536 |
0.61 |
|
| 2021 |
Mackey P, Turlik A, Ando K, Light ME, Houk KN, McGlacken GP. Stereoselective Installation of Five Contiguous Stereogenic Centers in a Double Aldol-Tishchenko Cascade and Evaluation of the Key Transition State through DFT Calculation. Organic Letters. PMID 34374288 DOI: 10.1021/acs.orglett.1c02179 |
0.388 |
|
| 2021 |
Turlik A, Ando K, Mackey P, Alcock E, Light M, McGlacken GP, Houk KN. Mechanism and Origins of Stereoselectivity of the Aldol-Tishchenko Reaction of Sulfinimines. The Journal of Organic Chemistry. PMID 33586983 DOI: 10.1021/acs.joc.0c02862 |
0.416 |
|
| 2020 |
Bogart JW, Kramer NJ, Turlik A, Bleich RM, Catlin DS, Schroeder FC, Nair SK, Williamson RT, Houk KN, Bowers AA. Interception of the "Bycroft-Gowland" intermediate in the enzymatic macrocyclization of thiopeptides. Journal of the American Chemical Society. PMID 32609512 DOI: 10.1021/Jacs.0C05639 |
0.36 |
|
| 2020 |
Debrauwer V, Turlik A, Rummler L, Prescimone A, Blanchard N, Houk KN, Bizet V. Ligand-Controlled Regiodivergent Palladium-Catalyzed Hydrogermylation of Ynamides. Journal of the American Chemical Society. PMID 32483965 DOI: 10.1021/Jacs.0C03556 |
0.327 |
|
| 2019 |
Turlik A, Chen Y, Scruse AC, Newhouse TR. Convergent Total Synthesis of Principinol D, a Rearranged Kaurane Diterpenoid. Journal of the American Chemical Society. PMID 31042866 DOI: 10.1021/Jacs.9B03751 |
0.634 |
|
| 2019 |
Elkin M, Scruse AC, Turlik A, Newhouse TR. Computational and Synthetic Investigation of Cationic Rearrangement in the Putative Biosynthesis of Justicane Triterpenoids. Angewandte Chemie (International Ed. in English). 58: 1025-1029. PMID 30575223 DOI: 10.1002/Anie.201810566 |
0.633 |
|
| 2016 |
Chen Y, Turlik A, Newhouse TR. Amide α,β-Dehydrogenation Using Allyl-Palladium Catalysis and a Hindered Monodentate Anilide. Journal of the American Chemical Society. PMID 26790471 DOI: 10.1021/Jacs.5B12924 |
0.754 |
|
| 2016 |
Newhouse T, Turlik A, Chen Y. Dehydrogenation Adjacent to Carbonyls Using Palladium–Allyl Intermediates Synlett. 27: e4-e4. DOI: 10.1055/S-0035-1560427 |
0.397 |
|
| 2016 |
Turlik A, Chen Y, Newhouse TR. Dehydrogenation Adjacent to Carbonyls Using Palladium-Allyl Intermediates Synlett. 27: 331-336. DOI: 10.1055/S-0035-1560427 |
0.735 |
|
| 2016 |
Turlik A, Chen Y, Newhouse TR. ChemInform Abstract: Dehydrogenation Adjacent to Carbonyls Using Palladium-Allyl Intermediates Cheminform. 47. DOI: 10.1002/CHIN.201621240 |
0.403 |
|
| Show low-probability matches. |