Christopher S. Jeffrey, Ph.D.

Affiliations: 
Chemistry University of Nevada, Reno, Reno, NV, United States 
Area:
organic chemistry
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Thomas Robert Hoye grad student 2004-2009 UMN
 (Studies of the synthesis and biology of petromyzonamine disulfate and the synthesis of (+)-scyphostatin.)
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Publications

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Uckele KA, Jahner JP, Tepe EJ, et al. (2021) Phytochemistry reflects different evolutionary history in traditional classes versus specialized structural motifs. Scientific Reports. 11: 17247
Decker LE, Jeffrey CS, Ochsenrider KM, et al. (2020) Elevated atmospheric concentrations of CO increase endogenous immune function in a specialist herbivore. The Journal of Animal Ecology
Maynard LD, Slinn HL, Glassmire AE, et al. (2020) Secondary metabolites in a neotropical shrub: spatiotemporal allocation and role in fruit defense and dispersal. Ecology. e03192
Glassmire AE, Philbin C, Richards LA, et al. (2019) Proximity to canopy mediates changes in the defensive chemistry and herbivore loads of an understory tropical shrub, Piper kelleyi. Ecology Letters. 22: 332-341
Richards LA, Oliveira C, Dyer LA, et al. (2018) Shedding Light on Chemically Mediated Tri-Trophic Interactions: A H-NMR Network Approach to Identify Compound Structural Features and Associated Biological Activity. Frontiers in Plant Science. 9: 1155
Philbin CS, Richards LA, Marion ZH, et al. (2018) Partitioning the phytochemical landscape F1000research. 7
Massad TJ, Martins de Moraes M, Philbin C, et al. (2017) Similarity in volatile communities leads to increased herbivory and greater tropical forest diversity. Ecology
Acharya A, Montes K, Jeffrey CS. (2016) Access to 4-Oxazolidinones: A (3 + 2) Cycloaddition Approach. Organic Letters. 18: 6082-6085
Glassmire AE, Jeffrey CS, Forister ML, et al. (2016) Intraspecific phytochemical variation shapes community and population structure for specialist caterpillars. The New Phytologist
Anumandla D, Acharya A, Jeffrey CS. (2016) Oxidative (3 + 2) Cycloaddition Reactions of Diaza-Oxyallyl Cationic Intermediates and Indoles for the Synthesis of Imidazoloindolines. Organic Letters
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