| Year |
Citation |
Score |
| 2024 |
Dalton DM, Walroth RC, Rouget-Virbel C, Mack KA, Toste FD. Utopia Point Bayesian Optimization Finds Condition-Dependent Selectivity for -Methyl Pyrazole Condensation. Journal of the American Chemical Society. PMID 38804885 DOI: 10.1021/jacs.4c01616 |
0.525 |
|
| 2024 |
Pompeo MM, Kelly SM, St-Jean F, Bass TM, Dalton DM, Zell D, Han C, Sirois LE, Gosselin F. Umpolung Flow Chemistry for the Synthesis of a 3-Oxo-3-spiro[benzofuran-2,4'-piperidine] Building Block. The Journal of Organic Chemistry. PMID 38767619 DOI: 10.1021/acs.joc.4c00337 |
0.342 |
|
| 2018 |
Hyster TK, Dalton DM, Rovis T. Correction: Ligand design for Rh(iii)-catalyzed C-H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones. Chemical Science. 9: 8024. PMID 30542552 DOI: 10.1039/C8Sc90195C |
0.722 |
|
| 2017 |
Hyster TK, Dalton DM, Rovis T. Correction: Ligand design for Rh(iii)-catalyzed C-H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones. Chemical Science. 8: 1666. PMID 30123475 DOI: 10.1039/c6sc90080a |
0.713 |
|
| 2015 |
Dalton DM, Ellis SR, Nichols EM, Mathies RA, Toste FD, Bergman RG, Raymond KN. Supramolecular Ga4L6(12-) Cage Photosensitizes 1,3-Rearrangement of Encapsulated Guest via Photoinduced Electron Transfer. Journal of the American Chemical Society. 137: 10128-31. PMID 26256754 DOI: 10.1021/Jacs.5B06317 |
0.592 |
|
| 2015 |
Chu JC, Dalton DM, Rovis T. Zn-catalyzed enantio- and diastereoselective formal [4 + 2] cycloaddition involving two electron-deficient partners: asymmetric synthesis of piperidines from 1-azadienes and nitro-alkenes. Journal of the American Chemical Society. 137: 4445-52. PMID 25821893 DOI: 10.1021/Jacs.5B00033 |
0.694 |
|
| 2015 |
Hyster TK, Dalton DM, Rovis T. Ligand Design for Rh(III)-Catalyzed C-H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective Synthesis of Dihydroisoquinolones. Chemical Science (Royal Society of Chemistry : 2010). 6: 254-258. PMID 25489470 DOI: 10.1039/C4Sc02590C |
0.755 |
|
| 2014 |
Oberg KM, Martin TJ, Oinen ME, Dalton DM, Friedman RK, Neely JM, Rovis T. Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use of Taddolpyrrolidine Phosphoramidite. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 91: 150-161. PMID 25346554 DOI: 10.15227/Orgsyn.091.0150 |
0.688 |
|
| 2013 |
Zhao X, Glover GS, Oberg KM, Dalton DM, Rovis T. SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 24. PMID 24379522 DOI: 10.1055/S-0033-1338842 |
0.751 |
|
| 2013 |
Dalton DM, Rappé AK, Rovis T. Perfluorinated Taddol Phosphoramidite as an L,Z-Ligand on Rh(I) and Co(-I): Evidence for Bidentate Coordination via Metal-C6F5 Interaction. Chemical Science (Royal Society of Chemistry : 2010). 4: 2062-2070. PMID 23671790 DOI: 10.1039/C3Sc50271F |
0.628 |
|
| 2013 |
Dalton DM, Rovis T. Catalytic, asymmetric indolizidinone aza-quaternary stereocenter synthesis: expedient synthesis of the cylindricine alkaloid core. Organic Letters. 15: 2346-9. PMID 23631448 DOI: 10.1021/Ol400529K |
0.691 |
|
| 2013 |
Rovis T, Dalton D. Rhodium-Catalyzed Enantioselective [2+2+2] Cycloaddition Synfacts. 9: 1030-1030. DOI: 10.1055/s-0033-1339688 |
0.656 |
|
| 2010 |
Dalton DM, Rovis T. Organometallic chemistry: C-H carboxylation takes gold. Nature Chemistry. 2: 710-1. PMID 20729887 DOI: 10.1038/Nchem.815 |
0.612 |
|
| 2009 |
Friedman RK, Oberg KM, Dalton DM, Rovis T. Phosphoramidite-Rhodium Complexes as Catalysts for the Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes. Pure and Applied Chemistry. Chimie Pure Et Appliquee. 82: 1353-1364. PMID 20622923 DOI: 10.1351/Pac-Con-09-12-09 |
0.779 |
|
| 2009 |
Dalton DM, Oberg KM, Yu RT, Lee EE, Perreault S, Oinen ME, Pease ML, Malik G, Rovis T. Enantioselective rhodium-catalyzed [2 + 2 + 2] cycloadditions of terminal alkynes and alkenyl isocyanates: mechanistic insights lead to a unified model that rationalizes product selectivity. Journal of the American Chemical Society. 131: 15717-28. PMID 19817441 DOI: 10.1021/Ja905065J |
0.748 |
|
| 2009 |
DiRocco DA, Oberg KM, Dalton DM, Rovis T. Catalytic asymmetric intermolecular stetter reaction of heterocyclic aldehydes with nitroalkenes: backbone fluorination improves selectivity. Journal of the American Chemical Society. 131: 10872-4. PMID 19722669 DOI: 10.1021/Ja904375Q |
0.729 |
|
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