Erika A. Crane, Ph.D. - Publications

Affiliations: 
2012 Chemistry Northwestern University, Evanston, IL 
Area:
Organic, Synthetic, Bio-Organic, Medicinal Chemistry, Chemical Biology, Catalysis, Materials

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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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