Erika A. Crane, Ph.D. - Publications
Affiliations: | 2012 | Chemistry | Northwestern University, Evanston, IL |
Area:
Organic, Synthetic, Bio-Organic, Medicinal Chemistry, Chemical Biology, Catalysis, MaterialsYear | Citation | Score | |||
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2023 | Matsuo B, Kim S, Shreiber ST, Levitre G, Li L, Crane EA, McClain EJ, Voight EA, Molander GA. Diversifying chemical space of DNA-encoded libraries: synthesis of 2-oxa-1-azaspiro(bicyclo[3.2.0])heptanes on-DNA visible light-mediated energy transfer catalysis. Chemical Communications (Cambridge, England). PMID 37608736 DOI: 10.1039/d3cc03421f | 0.32 | |||
2018 | Lee A, Betori R, Crane E, Scheidt KA. An Enantioselective Cross Dehydrogenative Coupling Catalysis Approach to Substituted Tetrahydropyrans. Journal of the American Chemical Society. PMID 29714480 DOI: 10.1021/Jacs.8B03063 | 0.583 | |||
2016 | Crane EA, Gademann K. Capturing Biological Activity in Natural Product Fragments by Chemical Synthesis. Angewandte Chemie (International Ed. in English). PMID 26833854 DOI: 10.1002/Anie.201505863 | 0.421 | |||
2011 | Crane EA, Zabawa TP, Farmer RL, Scheidt KA. Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations. Angewandte Chemie (International Ed. in English). 50: 9112-5. PMID 21932228 DOI: 10.1002/Anie.201102790 | 0.391 | |||
2011 | Wang J, Crane EA, Scheidt KA. Highly stereoselective Brønsted acid catalyzed synthesis of spirooxindole pyrans. Organic Letters. 13: 3086-9. PMID 21591768 DOI: 10.1021/Ol200987C | 0.627 | |||
2010 | Crane EA, Scheidt KA. Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis. Angewandte Chemie (International Ed. in English). 49: 8316-26. PMID 20931580 DOI: 10.1002/Anie.201002809 | 0.62 | |||
2010 | Crane EA, Scheidt KA. Die Prins-Makrocyclisierung als effiziente Ringschluss-Strategie in der Naturstoffsynthese Angewandte Chemie. 122: 8494-8505. DOI: 10.1002/Ange.201002809 | 0.447 | |||
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