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Chris Jamison - Publications

Affiliations: 
2014 Chemistry Princeton University, Princeton, NJ 
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11 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
2017 Garnsey MR, Slutskyy Y, Jamison CR, Zhao P, Lee J, Rhee YH, Overman LE. 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. PMID 29130687 DOI: 10.1021/Acs.Joc.7B02458  0.774
2017 Slutskyy Y, Jamison CR, Zhao P, Lee J, Rhee YH, Overman LE. 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. PMID 28514145 DOI: 10.1021/Jacs.7B04265  0.772
2016 Jamison CR, Overman LE. Fragment Coupling with Tertiary Radicals Generated by Visible-Light Photocatalysis. Accounts of Chemical Research. PMID 27491019 DOI: 10.1021/Acs.Accounts.6B00284  0.786
2016 Slutskyy Y, Jamison CR, Lackner GL, Müller DS, Dieskau AP, Unteidt NL, Overman LE. 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. PMID 27254137 DOI: 10.1021/Acs.Joc.6B00697  0.794
2016 Nawrat CC, Jamison CR, Slutskyy Y, MacMillan DW, Overman LE. 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. PMID 26820773 DOI: 10.1021/jacs.6b00456  0.757
2016 Nawrat CC, Jamison CR, Slutskyy Y, MacMillan DWC, Overman LE. ChemInform Abstract: Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling. Cheminform. 47: no-no. DOI: 10.1002/chin.201608055  0.785
2015 Nawrat CC, Jamison CR, Slutskyy Y, MacMillan DW, Overman LE. 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. PMID 26322524 DOI: 10.1021/Jacs.5B07678  0.762
2011 Harvey JS, Simonovich SP, Jamison CR, MacMillan DW. Enantioselective α-arylation of carbonyls via Cu(I)-bisoxazoline catalysis. Journal of the American Chemical Society. 133: 13782-5. PMID 21848265 DOI: 10.1021/Ja206050B  0.658
2009 Hilton CL, Jamison CR, Zane HK, King BT. A triphenylene-based triptycene with large free volume synthesized by zirconium-mediated biphenylation. The Journal of Organic Chemistry. 74: 405-7. PMID 19053591 DOI: 10.1021/Jo801643U  0.704
2007 King B, Hilton C, Jamison C. Zirconium-Mediated Biphenylation of Dihalobenzenes Synfacts. 2007: 0150-0150. DOI: 10.1055/s-2006-955810  0.707
2006 Hilton CL, Jamison CR, King BT. Uncatalyzed zirconium-mediated biphenylation of o-dihalobenzenes to form triphenylenes. Journal of the American Chemical Society. 128: 14824. PMID 17105290 DOI: 10.1021/Ja065602I  0.737
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