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Simon B. Lang, Ph.D.

Affiliations: 
2016- Chemistry University of Pennsylvania, Philadelphia, PA, United States 
Area:
Photoredox Dual Catalysis
Website:
http://molandergroup.chem.upenn.edu/slang.html
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"Simon Lang"

Parents

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Wayland E. Noland research assistant 2010-2011 UMN
Jon A. Tunge grad student 2011-2016 University of Kansas
Gary A. Molander post-doc 2016- Penn
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Publications

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Merchant RR, Lang SB, Yu T, et al. (2020) A General One-Pot Protocol for Hindered -Alkyl Azaheterocycles from Tertiary Carboxylic Acids. Organic Letters
Cartwright KC, Lang SB, Tunge JA. (2019) Photoinduced Kochi Decarboxylative Elimination for the Synthesis of Enamides and Enecarbamates from N-Acyl Amino Acids. The Journal of Organic Chemistry
Phelan JP, Lang SB, Sim J, et al. (2019) Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis. Journal of the American Chemical Society
Phelan JP, Wiles RJ, Lang SB, et al. (2018) Correction: Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies. Chemical Science. 9: 5119
Phelan JP, Lang SB, Compton JS, et al. (2018) Redox-Neutral Photocatalytic Cyclopropanation via Radical/Polar Crossover. Journal of the American Chemical Society
Phelan JP, Wiles RJ, Lang SB, et al. (2018) Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies. Chemical Science. 9: 3215-3220
Cabrera-Afonso MJ, Lu ZP, Kelly CB, et al. (2018) Engaging sulfinate salts Ni/photoredox dual catalysis enables facile C -SOR coupling. Chemical Science. 9: 3186-3191
Noland WE, Huisenga MP, Herzig RJ, et al. (2018) A Diels–Alder/Ene Cascade Leading to 5‐(Pyrrolidin‐3‐yl)thieno[3,2‐ e ]isoindoles from Ketone‐derived 2‐Vinylthiophenes and N ‐Phenylmaleimide Journal of Heterocyclic Chemistry. 55: 2698-2714
Molander G, Lang SB, Wiles RJ, et al. (2017) Photoredox Enables the Construction of 1,1-Difluoroalkene Carbonyl Mimics. Angewandte Chemie (International Ed. in English)
Matsui JK, Lang SB, Heitz DR, et al. (2017) Photoredox-Mediated Routes to Radicals: The Value of Catalytic Radical Generation in Synthetic Methods Development. Acs Catalysis. 7: 2563-2575
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