2019 – 2020
76. 2′-Alkynyl spin-labelling is a minimally perturbing tool for DNA structural analysis
J. S. Hardwick, M. M. Haugland, A. H. El-Sagheer, D. Ptchelkine,
F. R. Beierlein, A. N. Lane, T. Brown, J. E. Lovett, E. A. Anderson
Nucleic Acids Research, 2020, gkaa086. doi: 10.1093/nar/gkaa086
75. A Modular, Enantioselective Synthesis of Resolvins D3, E1, and Hybrids
F. Urbitsch, B. L. Elbert, J. Llaveria, P. E. Streatfeild, E. A. Anderson
Org. Lett., 2020. doi: 10.1021/acs.orglett.0c00089
74. Enantioselective synthesis and anti-parasitic properties of aporphine natural products
P. Pieper, E. McHugh, M. Amaral, A. G.Tempone, E. A.Anderson
Tetrahedron., 2019, 76, 130814. doi: 10.1016/j.tet.2019.130814
73. Synthesis of Cyclic Alkenyl Dimethylsiloxanes from Alkynyl Benzyldimethylsilanes and Application in Polyene Synthesis
H. G. Gudmundsson, C. J. Kuper, D. Cornut, F. Urbitsch, B. L. Elbert,
E. A. Anderson
J. Org. Chem., 2019, 84, 14868-14882. doi: 10.1021/acs.joc.9b01664
72. Convergent Total Syntheses of (–)-Rubriflordilactone B and (–)-pseudo-Rubriflordilactone B
M. Mohammad, V. Chintalapudi, J. M. Carney, S. J. Mansfield, P. Sanderson, K. E. Christensen, E. A. Anderson
Angew. Chem. Int. Ed., 2019. doi: 10.1002/anie.201908917
71. Rationalizing the diverse reactivity of [1.1.1]propellane through 𝜎-𝜋-delocalization
A. J. Sterling, A. B. Dürr, R. C. Smith,
E. A. Anderson, F. Duarte
ChemRxiv Preprint, doi: 10.26434/chemrxiv.9733628.v2
70. Dehydrodieugenol B derivatives as antiparasitic agents: Synthesis and biological activity against Trypanosoma cruzi
D. D. Ferreira, F. S. Sousa, T. A. Costa-Silva, J. Q. Reimão, A. C. Torrecilhas, D. M. Johns, C. E. Sear, K. M. Honorio, J. H. G. Lago, E. A. Anderson, A. G. Tempone
Eur. J. Med. Chem., 2019, 176, 162-174. doi: 10.1016/j.ejmech.2019.05.001
69. A semi-synthetic neolignan derivative from dihydrodieugenol B selectively affects the bioenergetic system of Leishmania infantum and inhibits cell division
M. Amaral, F. S. de Sousa, T. A. Costa Silva, A. Jimenez G. Junior, N. N. Taniwaki, D. M. Johns, J. H. G. Lago, E. A. Anderson & A. G. Tempone
Scientific Reports, 2019, 6, 6114. doi: 10.1038/s41598-019-42273-z
68. Silver-Catalyzed C- to N-Center Remote Arene Migration
Y. Ning, A. Mekareeya, K. R. Babu, E. A. Anderson and X. Bi
ACS Catalysis, 2019, 9, 4203-4210. doi: 10.1021/acscatal.9b00500
67. A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis.
J. Nugent, C. Arroniz, B. R. Shire, A. J. Sterling, H. D. Pickford, M. L. J. Wong, S. J. Mansfield, D. F. J. Caputo, B. Owen, J. J. Mousseau, F. Duarte and E. A. Anderson
ACS Catalysis, 2019, 9, 9568-9574. doi: 10.1021/acscatal.9b03190
66. A General Copper-Catalyzed Synthesis of Ynamides from 1,2-Dichloroenamides.
S. J. Mansfield, R. C. Smith, J. R. J. Yong, O. L. Garry, and E. A. Anderson
Org. Lett., 2019, 21, 2918-2922. doi: 10.1021/acs.orglett.9b00971.
65. Synthesis of Enantioenriched α-Chiral Bicyclo[1.1.1]pentanes.
M. L. J. Wong, J. J. Mousseau, S. J. Mansfield and E. A. Anderson.
Org. Lett., 2019, 21, 2408-2411. doi: 10.1021/acs.orglett.9b00691.
64. Palladium-catalysed ligand-free reductive Heck cycloisomerisation of 1,6-en-α-chloro-enamides.
Y. Hou, J. Ma, H. Yang, E. A. Anderson, A. Whiting and N. Wu.
Chem. Commun., 2019, 55, 3733-3736. doi: 10.1039/C9CC00537D.
63. Direct Transformation of Terminal Alkynes into Amidines by a Silver-Catalyzed Four-Component Reaction.
B. Liu, Y. Ning, M. Virelli, G. Zanoni, E. A. Anderson and X. Bi.
J. Am. Chem. Soc., 2019, 141, 1593-1598. doi: 10.1021/jacs.8b11039.
62. Use of trifluoroacetaldehyde N-tfsylhydrazone as a trifluorodiazoethane surrogate and its synthetic applications.
X. Zhang, Z. Liu, X. Yang, Y. Dong, M. Virelli, G. Zanoni, E. A. Anderson and X. Bi.
Nature Commun., 2019, 10, 284. doi: 10.1038/s41467-018-08253-z.
