[Baran lab]
[1]

  • Y. Kawamata, J.C. Vantourout, D.P. Hickey, P. Bai, L. Chen, Q. Hou, W. Qiao, K. Barman, M.A. Edwards, A.F. Garrido-Castro, J.N. deGruyter, H. Nakamura, K. Knouse, C. Qin, K.J. Clay, D. Bao, C. Li, J.T. Starr, C. Garcia-Irizarry, N. Sach, H.S. White, M. Neurock, S.D. Minteer, and P.S. Baran, "Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications", Journal of the American Chemical Society, vol. 141, pp. 6392-6402, 2019. http://dx.doi.org/10.1021/jacs.9b01886
  • [1]

  • A. Barthelemy, E. Anselmi, T. Le, G. Vo-Thanh, R. Guillot, K. Miqueu, and E. Magnier, "Divergent Synthesis of 1,2-Benzo[e]thiazine and Benzo[d]thiazole Analogues Containing a S-Trifluoromethyl Sulfoximine Group: Preparation and New Properties of the Adachi Reagent", The Journal of Organic Chemistry, vol. 84, pp. 4086-4094, 2019. http://dx.doi.org/10.1021/acs.joc.9b00079
  • Further developments of the “computer-aided synthesis planning” software Chematica (bought by Merck and further developed as ‘Synthia’):

    [1]
  • T. Badowski, K. Molga, and B.A. Grzybowski, "Selection of cost-effective yet chemically diverse pathways from the networks of computer-generated retrosynthetic plans", Chemical Science, vol. 10, pp. 4640-4651, 2019. http://dx.doi.org/10.1039/C8SC05611K