Douglas Carl Behenna, Ph.D.
Affiliations: | 2007 | Chemistry | California Institute of Technology, Pasadena, CA |
| 2012- | Pfizer, Inc., San Diego, CA, United States |
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"Douglas Behenna"Mean distance: 7.2 | S | N | B | C | P |
Parents
Sign in to add mentor| Brian M. Stoltz | grad student | 2007 | Caltech | |
| (Progress Toward the Synthesis of (+)-Zoanthenol And The Development of an Asymmetric Tsuji Allylation Reaction.) | ||||
| Elias James Corey | post-doc | 2006-2010 | Harvard | |
| Brian M. Stoltz | research scientist | 2010-2012 | Caltech | |
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Publications
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| Bagdanoff JT, Behenna DC, Stockdill JL, et al. (2016) Enantioselective Synthesis of Caprolactam and Enone Precursors to the Heterocyclic DEFG Ring System of Zoanthenol. European Journal of Organic Chemistry. 2016: 2101-2104 |
| Craig RA, Loskot SA, Mohr JT, et al. (2015) Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones. Organic Letters. 17: 5160-3 |
| Korch KM, Eidamshaus C, Behenna DC, et al. (2015) Enantioselective synthesis of α-secondary and α-tertiary piperazin-2-ones and piperazines by catalytic asymmetric allylic alkylation. Angewandte Chemie (International Ed. in English). 54: 179-83 |
| Liu Y, Liniger M, McFadden RM, et al. (2014) Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation. Beilstein Journal of Organic Chemistry. 10: 2501-12 |
| Reeves CM, Behenna DC, Stoltz BM. (2014) Development of (trimethylsilyl)ethyl ester protected enolates and applications in palladium-catalyzed enantioselective allylic alkylation: intermolecular cross-coupling of functionalized electrophiles. Organic Letters. 16: 2314-7 |
| Krishnan S, Shanmuganathan MV, Behenna D, et al. (2014) Angiotensin II receptor type 1--a novel target for preventing neonatal meningitis in mice by Escherichia coli K1. The Journal of Infectious Diseases. 209: 409-19 |
| Bennett NB, Duquette DC, Kim J, et al. (2013) Expanding insight into asymmetric palladium-catalyzed allylic alkylation of N-heterocyclic molecules and cyclic ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4414-8 |
| Behenna DC, Stoltz BM. (2013) Natural products as inspiration for reaction development: Catalytic enantioselective decarboxylative reactions of prochiral enolate equivalents Topics in Organometallic Chemistry. 44: 281-313 |
| Keith JA, Behenna DC, Sherden N, et al. (2012) The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation. Journal of the American Chemical Society. 134: 19050-60 |
| Behenna DC, Liu Y, Yurino T, et al. (2012) Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams. Nature Chemistry. 4: 130-3 |