Erika A. Crane, Ph.D.
Affiliations: | 2012 | Chemistry | Northwestern University, Evanston, IL |
Area:
Organic, Synthetic, Bio-Organic, Medicinal Chemistry, Chemical Biology, Catalysis, MaterialsGoogle:
"Erika Crane"Mean distance: 8.3 | S | N | B | C | P |
Cross-listing: Materials Tree
Parents
Sign in to add mentorKarl A. Scheidt | grad student | 2012 | Northwestern | |
(I. Total Synthesis and Biological Evaluation of (--)-Exiguolide II. Development of Prins-Type Cyclization Methods.) |
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Publications
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Matsuo B, Kim S, Shreiber ST, et al. (2023) 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) |
Lee A, Betori R, Crane E, et al. (2018) An Enantioselective Cross Dehydrogenative Coupling Catalysis Approach to Substituted Tetrahydropyrans. Journal of the American Chemical Society |
Crane EA, Gademann K. (2016) Capturing Biological Activity in Natural Product Fragments by Chemical Synthesis. Angewandte Chemie (International Ed. in English) |
Crane EA, Zabawa TP, Farmer RL, et al. (2011) Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations. Angewandte Chemie (International Ed. in English). 50: 9112-5 |
Wang J, Crane EA, Scheidt KA. (2011) Highly stereoselective Brønsted acid catalyzed synthesis of spirooxindole pyrans. Organic Letters. 13: 3086-9 |
Crane EA, Scheidt KA. (2010) Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis. Angewandte Chemie (International Ed. in English). 49: 8316-26 |
Crane EA, Scheidt KA. (2010) Die Prins-Makrocyclisierung als effiziente Ringschluss-Strategie in der Naturstoffsynthese Angewandte Chemie. 122: 8494-8505 |