2019 – 2020

77. Synthesis of All-carbon Disubstituted Bicyclo[1.1.1]pentanes by Iron-Catalyzed Kumada Cross-Coupling

 

J. Nugent,* B. R. Shire,*, D. F. J. Caputo, H. D. Pickford, F. Nightingale, I. T. T. Houlsby, J. J. Mousseau,  E. A. Anderson

*equal author contribution

 

Angew. Chem. Int. Ed., 2020, doi10.1002/anie.202004090

76. 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

 

Chem. Sci., 2020, doi: 10.1039/D0SC01386B

75. 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. doi10.1093/nar/gkaa086

74. 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., 202022, 1510–1515. doi: 10.1021/acs.orglett.0c00089

73. 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

72. 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., 201984, 14868-14882. doi: 10.1021/acs.joc.9b01664

71. 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., 201958, 18177–18181. 

doi: 10.1002/anie.201908917

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

*equal author contribution

 

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.

©2018 by Ed Anderson Group.