Michelle R. Garnsey, Ph.D. - Publications

Affiliations: 
2012 Chemistry Duke University, Durham, NC 

14 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
2020 Schmidt OP, Dechert‐Schmitt A, Garnsey MR, Wisniewska HM, Blackmond DG. Corrigendum: Kinetic Analysis of Catalytic Organic Reactions Using a Temperature Scanning Protocol Chemcatchem. DOI: 10.1002/Cctc.202000437  0.357
2019 Liao J, Basch CH, Hoerrner ME, Talley MR, Boscoe BP, Tucker JW, Garnsey MR, Watson MP. Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides. Organic Letters. PMID 30917282 DOI: 10.1021/Acs.Orglett.9B01014  0.425
2019 Dechert-Schmitt A, Garnsey MR, Wisniewska HM, Murray JI, Lee T, Kung DW, Sach N, Blackmond DG. Highly Modular Synthesis of 1,2-Diketones via Multicomponent Coupling Reactions of Isocyanides as CO Equivalents Acs Catalysis. 9: 4508-4515. DOI: 10.1021/Acscatal.9B00581  0.466
2019 Schmidt OP, Dechert‐Schmitt A, Garnsey MR, Wisniewska HM, Blackmond DG. Kinetic Analysis of Catalytic Organic Reactions Using a Temperature Scanning Protocol Chemcatchem. 11: 3808-3813. DOI: 10.1002/Cctc.201900560  0.357
2018 Liao J, Guan W, Boscoe BP, Tucker JW, Tomlin JW, Garnsey MR, Watson MP. Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C-N Bond Activation. Organic Letters. PMID 29745674 DOI: 10.1021/Acs.Orglett.8B01062  0.451
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  0.445
2015 Davoren JE, O'Neil SV, Anderson DP, Brodney MA, Chenard L, Dlugolenski K, Edgerton JR, Green M, Garnsey M, Grimwood S, Harris AR, Kauffman GW, LaChapelle E, Lazzaro JT, Lee CW, et al. Design and optimization of selective azaindole amide M1 positive allosteric modulators. Bioorganic & Medicinal Chemistry Letters. PMID 26631313 DOI: 10.1016/J.Bmcl.2015.11.053  0.312
2015 Garnsey MR, Uteuliyev MM, Coltart DM. Asymmetric synthesis of structural analogues of (+)-clusianone via enantioselective ACC alkylation Tetrahedron Letters. 56: 3183-3185. DOI: 10.1016/J.Tetlet.2015.01.012  0.708
2011 Garnsey MR, Matous JA, Kwiek JJ, Coltart DM. Asymmetric total synthesis of (+)- and (-)-clusianone and (+)- and (-)-clusianone methyl enol ether via ACC alkylation and evaluation of their anti-HIV activity. Bioorganic & Medicinal Chemistry Letters. 21: 2406-9. PMID 21414776 DOI: 10.1016/J.Bmcl.2011.02.074  0.64
2010 Garnsey MR, Lim D, Yost JM, Coltart DM. Development of a strategy for the asymmetric synthesis of polycyclic polyprenylated acylphloroglucinols via N-amino cyclic carbamate hydrazones: application to the total synthesis of (+)-clusianone. Organic Letters. 12: 5234-7. PMID 20977254 DOI: 10.1021/Ol1022728  0.701
2010 Sauer SJ, Garnsey MR, Coltart DM. Direct carbon-carbon bond formation via reductive soft enolization: a kinetically controlled syn-aldol addition of α-halo thioesters and enolizable aldehydes. Journal of the American Chemical Society. 132: 13997-9. PMID 20849119 DOI: 10.1021/Ja1057407  0.754
2010 Kohler MC, Yost JM, Garnsey MR, Coltart DM. Direct carbon-carbon bond formation via soft enolization: a biomimetic asymmetric Mannich reaction of phenylacetate thioesters. Organic Letters. 12: 3376-9. PMID 20608684 DOI: 10.1021/Ol101152B  0.693
2010 Coltart D, Sauer S, Garnsey M. Reductive Enolization in Aldol Addition to Enolizable Aldehydes Synfacts. 2010: 1388-1388. DOI: 10.1055/s-0030-1258895  0.74
2009 Yost JM, Garnsey MR, Kohler MC, Coltart DM. Direct carbon-carbon bond formation via soft enolization of thioesters: An operationally simple mannich addition reaction Synthesis. 56-58. DOI: 10.1055/S-0028-1083278  0.688
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