Peter Somfai

Professor
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  1. 2019
  2. 2017
  3. An Efficient Synthesis of (±)-Dehaloperophoramidine

    Anita Hoang, Popov, K. & Peter Somfai, 2017 Feb 17, In : Journal of Organic Chemistry. 82, 4, p. 2171-2176 6 p.

    Research output: Contribution to journalArticle

  4. Total Synthesis of Dehaloperophoramidine: Evolution of a Synthesis

    Danielsson, J., Popov, K., Seashore-Ludlow, B. & Peter Somfai, 2017, Strategies and Tactics in Organic Synthesis. Academic Press, Vol. 13. p. 217-242 26 p. (Strategies and Tactics in Organic Synthesis; vol. 13).

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  5. 2016
  6. Synthesis of α-Keto Amides by a Pyrrolidine/TEMPO-Mediated Oxidation of α-Keto Amines

    Lu Yu & Peter Somfai, 2016 Nov 14, In : Synlett. 27, 18, p. 2587-2590 4 p., st-2016-b0315-l.

    Research output: Contribution to journalArticle

  7. Synthesis of Imidates: TFA-Mediated Regioselective Amide Alkylation Using Meerwein's Reagent

    Popov, K. & Peter Somfai, 2016 Apr 15, In : Journal of Organic Chemistry. 81, 8, p. 3470-3472 3 p.

    Research output: Contribution to journalArticle

  8. 2015
  9. A Diels-Alder Approach to a Communesin Model: A/B-Cyclization Route

    Sanzone, A. & Peter Somfai, 2015, In : European Journal of Organic Chemistry. 16, p. 3441-3449

    Research output: Contribution to journalArticle

  10. Concise Total Synthesis of Dehaloperophoramidine.

    Popov, K., Anita Hoang & Peter Somfai, 2015, In : Angewandte Chemie (International edition).

    Research output: Contribution to journalArticle

  11. 2014
  12. Studies Toward Communesin F: A Diels-Alder Approach.

    Danielsson, J. & Peter Somfai, 2014, In : Organic Letters. 16, 3, p. 784-787

    Research output: Contribution to journalArticle

  13. 2013
  14. 2012
  15. Asymmetric Transfer Hydrogenation Coupled with Dynamic Kinetic Resolution in Water: Synthesis of anti-β-Hydroxy-α-amino Acid Derivatives.

    Seashore-Ludlow, B., Saint-Dizier, F. & Peter Somfai, 2012, In : Organic Letters. 14, 24, p. 6334-6337

    Research output: Contribution to journalArticle