The present review gives an overview over non-toxic cyanation agents and cyanide sources used in the synthesis of structurally diverse products containing the nitrile function. Nucleophilic as well as electrophilic agents/systems that transfer the entire CN-group were taken in consideration. Reactions in whi
Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos–Ni(I) species
Copper-Mediated Transformation of Organosilanes to Nitriles with
Optimization of Reaction Conditions for Reduction of Benzoyl Cyanide
11C-, 12C-, and 13C-cyanation of electron-rich arenes via organic photoredox catalysis - ScienceDirect
Molecules, Free Full-Text
Non-toxic cyanide sources and cyanating agents - Organic
Fabrication of Pd Nanoparticles Embedded C@Fe3O4 Core–Shell Hybrid
Molecules, Free Full-Text
PDF] Cu-Catalyzed direct cyanation of terminal alkynes with AMBN or AIBN as the cyanation reagent.
PDF) Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos–Ni(I) species
Light-Triggered, Ni-Catalyzed Cyanation of Aryl Triflates with 1,4-Dicyanobenzene as the CN Source
氰化氢- 维基百科，自由的百科全书
Copper-catalyzed direct cyanation of terminal alkynes with benzoyl cyanide - ScienceDirect
