Year |
Citation |
Score |
2020 |
Meyer SM, Charlesworth-Seiler EM, Patrow JG, Kitzrow JP, Gerlach DL, Reinheimer EW, Dahl BJ. Synthesis and optical properties of a library of multi-colored isomeric aryldibenzopyrylium halochromic cations Tetrahedron. 76: 131222. DOI: 10.1016/j.tet.2020.131222 |
0.251 |
|
2017 |
Hintz HA, Sortedahl NJ, Meyer SM, Decato DA, Dahl BJ. The synthesis of lactone-bridged 1,3,5-triphenylbenzene derivatives as pi-expanded coumarin triskelions. Tetrahedron Letters. 58: 4703-4708. PMID 29430066 DOI: 10.1016/j.tetlet.2017.11.010 |
0.292 |
|
2015 |
Dressler JJ, Miller SA, Meeuwsen BT, Riel AMS, Dahl BJ. Synthesis of dilactone bridged terphenyls with crankshaft architectures Tetrahedron. 71: 283-292. DOI: 10.1016/j.tet.2014.11.055 |
0.255 |
|
2012 |
Carlson EJ, Riel AMS, Dahl BJ. Donor-acceptor biaryl lactones: PH induced molecular switches with intramolecular charge transfer modulation Tetrahedron Letters. 53: 6245-6249. DOI: org/10.1016/j.tetlet.2012.09.016 |
0.387 |
|
2012 |
Prust EE, Carlson EJ, Dahl BJ. 6-Aryldibenzo[b,d]pyrylium salts: Synthesis and characterization of a reversible pH-driven optical and spectroscopic response Tetrahedron Letters. 53: 6433-6435. DOI: 10.1016/j.tetlet.2012.09.054 |
0.282 |
|
2011 |
Mills NS, Cheng FE, Baylan JM, Tirla C, Hartmann JL, Patel KC, Dahl BJ, McClintock SP. Dications of 3-phenyl-indenylidene dibenzo[a.d]cycloheptene: the role of charge in the antiaromaticity of cationic systems. The Journal of Organic Chemistry. 76: 645-53. PMID 21190365 DOI: 10.1021/jo102220y |
0.614 |
|
2008 |
Dahl BJ, Mills NS. Antiaromaticity in distal bisfluorenyl dications separated by multiple discrete spacer units. Organic Letters. 10: 5605-8. PMID 19053742 DOI: 10.1021/ol802389n |
0.605 |
|
2008 |
Dahl BJ, Mills NS. Antiaromatic spacer-bridged bisfluorenyl dications generated by superacid induced ionization. Journal of the American Chemical Society. 130: 10179-86. PMID 18620392 DOI: 10.1021/ja711501k |
0.642 |
|
2006 |
Dahl BJ, Branchaud BP. 180 degree unidirectional bond rotation in a biaryl lactone artificial molecular motor prototype. Organic Letters. 8: 5841-4. PMID 17134286 DOI: 10.1021/ol062428u |
0.576 |
|
2005 |
Lin Y, Dahl BJ, Branchaud BP. Net directed 180° aryl-aryl bond rotation in a prototypical achiral biaryl lactone synthetic molecular motor Tetrahedron Letters. 46: 8359-8362. DOI: 10.1016/j.tetlet.2005.09.151 |
0.584 |
|
2004 |
Dahl BJ, Branchaud BP. Synthesis and characterization of a functionalized chiral biaryl capable of exhibiting unidirectional bond rotation Tetrahedron Letters. 45: 9599-9602. DOI: 10.1016/j.tetlet.2004.10.147 |
0.575 |
|
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