| Year |
Citation |
Score |
| 2019 |
Lee C, Vandenbrande J, Goetz AE, Ganter MA, Storti DW, Boydston AJ. Room temperature extrusion 3D printing of polyether ether ketone using a stimuli-responsive binder Additive Manufacturing. 28: 430-438. DOI: 10.17632/Cyt9Swmvtb.1 |
0.561 |
|
| 2017 |
Lin JB, Shah TK, Goetz A, Garg NK, Houk KN. Conjugated Trimeric Scaffolds Accessible From Indolyne Cyclotrimerizations: Synthesis, Structures, and Electronic Properties. Journal of the American Chemical Society. PMID 28675700 DOI: 10.1021/Jacs.7B05317 |
0.654 |
|
| 2017 |
Pascual LM, Goetz AE, Roehrich AM, Boydston AJ. Investigation of Tacticity and Living Characteristics of Photoredox-Mediated Metal-Free Ring-Opening Metathesis Polymerization. Macromolecular Rapid Communications. PMID 28195676 DOI: 10.1002/Marc.201600766 |
0.516 |
|
| 2016 |
Goetz AE, Pascual LMM, Dunford DG, Ogawa KA, Knorr DB, Boydston AJ. Expanded Functionality of Polymers Prepared Using Metal-Free Ring-Opening Metathesis Polymerization. Acs Macro Letters. 5: 579-582. PMID 35632374 DOI: 10.1021/acsmacrolett.6b00131 |
0.711 |
|
| 2016 |
Ogawa KA, Goetz AE, Boydston AJ. Developments in externally regulated ring-opening metathesis polymerization Synlett. 27: 203-214. DOI: 10.1055/S-0035-1560213 |
0.522 |
|
| 2016 |
Goetz AE, Pascual LMM, Dunford DG, Ogawa KA, Knorr DB, Boydston AJ. Expanded Functionality of Polymers Prepared Using Metal-Free Ring-Opening Metathesis Polymerization Acs Macro Letters. 5: 579-582. DOI: 10.1021/Acsmacrolett.6B00131 |
0.669 |
|
| 2015 |
Goetz AE, Boydston AJ. Metal-Free Preparation of Linear and Cross-Linked Polydicyclopentadiene. Journal of the American Chemical Society. 137: 7572-5. PMID 26053254 DOI: 10.1021/Jacs.5B03665 |
0.544 |
|
| 2015 |
Ogawa KA, Goetz AE, Boydston AJ. Metal-free ring-opening metathesis polymerization. Journal of the American Chemical Society. 137: 1400-3. PMID 25573294 DOI: 10.1021/Ja512073M |
0.556 |
|
| 2015 |
Goetz AE, Shah TK, Garg NK. Pyridynes and indolynes as building blocks for functionalized heterocycles and natural products. Chemical Communications (Cambridge, England). 51: 34-45. PMID 25226878 DOI: 10.1039/C4Cc06445C |
0.581 |
|
| 2015 |
Pascual LMM, Dunford DG, Goetz AE, Ogawa KA, Boydston AJ. Comparison of Pyrylium and Thiopyrylium Photooxidants in Metal-Free Ring-Opening Metathesis Polymerization Synlett. DOI: 10.1055/S-0035-1561330 |
0.686 |
|
| 2014 |
Goetz AE, Silberstein AL, Corsello MA, Garg NK. Concise enantiospecific total synthesis of tubingensin A. Journal of the American Chemical Society. 136: 3036-9. PMID 24524351 DOI: 10.1021/Ja501142E |
0.64 |
|
| 2014 |
Goetz AE, Garg NK. Enabling the use of heterocyclic arynes in chemical synthesis. The Journal of Organic Chemistry. 79: 846-51. PMID 24410270 DOI: 10.1021/Jo402723E |
0.531 |
|
| 2013 |
Goetz AE, Garg NK. Regioselective reactions of 3,4-pyridynes enabled by the aryne distortion model. Nature Chemistry. 5: 54-60. PMID 23247178 DOI: 10.1038/Nchem.1504 |
0.562 |
|
| 2012 |
Goetz AE, Bronner SM, Cisneros JD, Melamed JM, Paton RS, Houk KN, Garg NK. An efficient computational model to predict the synthetic utility of heterocyclic arynes. Angewandte Chemie (International Ed. in English). 51: 2758-62. PMID 22307724 DOI: 10.1002/Anie.201108863 |
0.646 |
|
| 2011 |
Bronner SM, Goetz AE, Garg NK. Overturning indolyne regioselectivities and synthesis of indolactam V. Journal of the American Chemical Society. 133: 3832-5. PMID 21351773 DOI: 10.1021/Ja200437G |
0.682 |
|
| 2011 |
Bronner SM, Goetz AE, Garg NK. Understanding and modulating indolyne regioselectivities Synlett. 2599-2604. DOI: 10.1055/S-0031-1289561 |
0.671 |
|
| 2010 |
Im GY, Bronner SM, Goetz AE, Paton RS, Cheong PH, Houk KN, Garg NK. Indolyne experimental and computational studies: synthetic applications and origins of selectivities of nucleophilic additions. Journal of the American Chemical Society. 132: 17933-44. PMID 21114321 DOI: 10.1021/Ja1086485 |
0.692 |
|
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