©2018 by Ed Anderson Group.


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. 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. Straining to react: Delocalization Drives the Stability and Omniphilicity of [1.1.1]Propellane


A. J. Sterling, A. B. Dürr, R. C. Smith,

E. A. Anderson, F. Duarte


ChemRxiv Preprint, doi: 10.26434/chemrxiv.9733628.v1

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 Reports2019, 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 Catalysis2019, 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 Catalysis2019, 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, 284doi: 10.1038/s41467-018-08253-z.

61. Four Step Total Synthesis of an H3 Receptor Antagonist Using Only Tools Found in a Typical Teaching Laboratory.

C. J. Smith, S. J. Mansfield, E. A. Anderson and J. W. Burton. 


J. Chem. Educ., 2019, 96, 137-142doi: 10.1021/acs.jchemed.7b00982.