1205676-37-4Relevant articles and documents
Unraveling the C2-Symmetric Azatetraquinane System. Simple, Enantioselective Syntheses
Reddy, G. Sudhakar,Reddy, D. Srinivas,Corey
, p. 2258 - 2262 (2021)
Concise stereocontrolled synthetic routes to the C2-symmetric azatetraquinane 1 (or, also, the enantiomer) are described. The successful execution of the synthesis involved innovation in the methodology for [3+2] cycloaddition and stereochemical control.
Enantioselective biocatalytic oxidative desymmetrization of substituted pyrrolidines
Koehler, Valentin,Bailey, Kevin R.,Znabet, Anass,Raftery, James,Helliwell, Madeleine,Turner, Nicholas J.
supporting information; experimental part, p. 2182 - 2184 (2010/06/18)
"Chemical Equation Presented" Center stage: Additions of nitrogen-centered radicals to cyanamide compounds provided the first radical synthesis of aromatic polycyclic guanidine derivatives (see scheme). Modular assembly of the substrates allows for a rapid increase of the molecular complexity of scaffolds, which have potential applications for medicinal chemistry.