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Bjorn C. G. Soderberg, Ph.D.

Professor EMERITUS

About

Ph.D., Royal Institute of Technology, Stockholm, Sweden

Dr. Soderberg's research interests include the development of novel synthetic methodology based on transition metal catalyzed or mediated reactions and synthesis of biologically active products. 

Teaching Fields

Organic Chemistry

Courses Offered 

  • CHEM 233
  • CHEM 234
  • CHEM 235
  • CHEM 236
  • CHEM 335 

Publications

Ganesh Ghimire and B. C. G. Söderberg, “Short syntheses of the tricyclic indole alkaloids cimitrypazepine and fargesine.” Tetrahedron Lett. 201657, 3873-3876.

N. H. Ansari and B. C. G. Söderberg, “Short syntheses of the indole alkaloids alocasin A, scalaridine A, and hyrtinadine A-B.” Tetrahedron 201672, 2414-2421.

Y. Zhang, I. W. McArdle, J. W. Hubbard, N. G. Akhmedov, and B. C. G. Söderberg, “Total synthesis of the tetracyclic indole alkaloid ht-13-A.” Tetrahedron Lett. 201657, 2865-2867.

Y. Zhang, J. W. Hubbard, N. G. Akhmedov, J. L. Petersen, B. C. G. Söderberg, “Total synthesis of the tetracyclic indole alkaloid ht-13-B.” J. Org. Chem. 201580, 4783-4790.

M. M. Cummings, B. C. G. Söderberg, “Reexamination of the bromination of 2-nitro-benzaldehyde with NBS or NaBr-NaIO4 in sulfuric acid.” Synth. Commun. 201444, 1-5.

H. Yin, S. W. Dantale, N. G. Akhmedov, and B. C. G. Söderberg, “Formation of 2-halomethylene-4-cyclopentene-1,3-diones and/or 2-halo-1,4-benzoquinones via ring-expansion of 4-ethynyl-4-hydroxy-2,3-substituted-2-cyclobuten-1-ones. Total synthesis of methyl linderone.” Tetrahedron 201369, 9284-9293.

M. M. Cummings, R. W. Clawson Jr., S. B. Sharma, R. A. Byerly, N. G. Akhmedov, B. C. G. Söderberg, “An expedient synthesis of salviadione.” Tetrahedron 2011, 67, 4753-4757.

S. R. Banini, M. R. Turner, M. M. Cummings, B. C. G. Söderberg, “A base-modulated chemoselective synthesis of 3-cyanoindoles or 4-cyanoquinolines using a palladium-catalyzed N-heterocyclization.” Tetrahedron 2011, 67, 3603-3611.

B. C. G. Söderberg, J. A. Shriver, and J. M. Wallace, “Synthesis of Indoles by Palladium Catalyzed Reductive N-Heteroannulation of 2-Nitrostyrenes: Methyl Indole-4-carboxylate” Org. Synth. Discuss. Addendum 2011, 88, 291-295. 

S. P. Gorugantula, G. M. Carrero-Martínez, S. W. Dantale, B. C. G. Söderberg, “Palladium-catalyzed reductive N-heterocyclization of alkenyl-substituted nitroarenes as a viable method for the preparation of bicyclic pyrrolo-fused heteroaromatic compounds.” Tetrahedron 2010, 66, 1800-1805.

N. G. Akhmedov, C. A. Dacko, A. Güven, B. C. G. Söderberg, “Complete Assignment of the 1H and 13C NMR Spectra of Monosubstituted 3-([(2R,5S)-5-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]methyl)-1H-indoles Using the Gradient Selected gCOSY, gHSQC and gHMBC Techniques”, Magn. Reson. Chem. 2010, 48, 134-150.

Book Chapters and Reviews

L. S. Hegedus, B. C. G. Söderberg, “Transition Metals in the Synthesis of Complex Organic Molecules.” Third Ed.; University Science Books. 2009.

B. C. G. Söderberg, “Transition Metals in Organic Synthesis: Highlights for the Year 2005.” Coord. Chem. Rev. 2008, 252, 57-133. 

B. C. G. Söderberg, “Transition Metals in Organic Synthesis: Highlights for the Year 2004.” Coord. Chem. Rev. 2006, 250, 2411-2490.

B. C. G. Söderberg, “Transition Metals in Organic Synthesis: Highlights for the Year 2003.” Coord. Chem. Rev. 2006, 250, 300-387.

B. C. G. Söderberg, “Transition Metals in Organic Synthesis: Transition Metal Carbonyl Complexes.” In “Encyclopedia of Inorganic Chemistry, Second Ed., “Charles M. Lukehart Ed.; John Wiley & Sons, 2005.