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Beilstein Journal of Organic Chemistry|December 1, 2018
Synthesis of α-D-GalpN3-(1-3)-D-GalpN3: α- and 3-O-selectivity using 3,4-diol acceptorsEmil Glibstrup, Christian Marcus PedersenOrganic & Biomolecular Chemistry|January 14, 2017
On the nature of the electronic effect of multiple hydroxyl groups in the 6-membered ring - the effects are additive but steric hindrance plays a role tooChristian Marcus Pedersen, Mikael BolsChemical Science|June 23, 2022
Vessel effects in organic chemical reactions; a century-old, overlooked phenomenonMichael Martin Nielsen, Christian Marcus PedersenOrganic & Biomolecular Chemistry|June 3, 2024
Influence of remote carbamate protective groups on the β-selectivity in rhamnosylationsAsger Munk Koue, Christian Marcus PedersenCarbohydrate Research|January 16, 2022
Slow glycosylation: Activation of trichloroacetimidates under mild conditions using lithium salts and the role of counterionsNora Katharina Korber, Christian Marcus PedersenChemical Reviews|July 4, 2018
Catalytic Glycosylations in Oligosaccharide SynthesisMichael Martin Nielsen, Christian Marcus PedersenAngewandte Chemie (International Ed. in English)|October 7, 2020
Reactivity, Selectivity, and Synthesis of 4-C-Silylated Glycosyl Donors and 4-Deoxy AnaloguesMartin Jaeger Pedersen, Christian Marcus PedersenChemical Record (New York, N.Y.)|May 24, 2021
Self-Promoted Stereoselective Glycosylations - Past, Present, FutureNatasha Videcrantz Faurschou, Christian Marcus PedersenChemical Science|July 23, 2025
Discovery of novel glycosylation methods using Bayesian optimization: lithium salt directed stereoselective glycosylationsNatasha Videcrantz Faurschou, Christian Marcus PedersenThe Journal of Organic Chemistry|June 22, 2013
Conformationally armed 3,6-tethered glycosyl donors: synthesis, conformation, reactivity, and selectivityMads Heuckendorff, Christian Marcus Pedersen, Mikael BolsPageof 6