Christopher Robert Jamison

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2014 Chemistry Princeton University, Princeton, NJ 
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"Christopher Jamison"
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David W.C. MacMillan grad student 2014 Princeton
 (Enantioselective arylations utilizing copper catalysts and diaryliodonium salts.)
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Jamison CR, Badillo JJ, Lipshultz JM, et al. (2017) Catalyst-controlled oligomerization for the collective synthesis of polypyrroloindoline natural products. Nature Chemistry. 9: 1165-1169
Garnsey MR, Slutskyy Y, Jamison CR, et al. (2017) Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C via Convergent Fragment Coupling Using a Tertiary Carbon Radical. The Journal of Organic Chemistry
Slutskyy Y, Jamison CR, Zhao P, et al. (2017) Versatile Construction of 6-Substituted cis-2,8-Dioxabicyclo[3.3.0]octan-3-ones. Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C. Journal of the American Chemical Society
Jamison CR, Overman LE. (2016) Fragment Coupling with Tertiary Radicals Generated by Visible-Light Photocatalysis. Accounts of Chemical Research
Slutskyy Y, Jamison CR, Lackner GL, et al. (2016) Short Enantioselective Total Syntheses of trans-Clerodane Diterpenoids: Convergent Fragment Coupling Using a trans-Decalin Tertiary Radical Generated from a Tertiary Alcohol Precursor. The Journal of Organic Chemistry
Nawrat CC, Jamison CR, Slutskyy Y, et al. (2016) Correction to "Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling". Journal of the American Chemical Society
Nawrat CC, Jamison CR, Slutskyy Y, et al. (2015) Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling. Journal of the American Chemical Society. 137: 11270-3
Harvey JS, Simonovich SP, Jamison CR, et al. (2011) Enantioselective α-arylation of carbonyls via Cu(I)-bisoxazoline catalysis. Journal of the American Chemical Society. 133: 13782-5
Hilton CL, Jamison CR, Zane HK, et al. (2009) A triphenylene-based triptycene with large free volume synthesized by zirconium-mediated biphenylation. The Journal of Organic Chemistry. 74: 405-7
Hilton CL, Jamison CR, King BT. (2006) Uncatalyzed zirconium-mediated biphenylation of o-dihalobenzenes to form triphenylenes. Journal of the American Chemical Society. 128: 14824
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