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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
SciELO - Brazil - RECENT ADVANCES IN CYANATION REACTIONS RECENT ADVANCES IN CYANATION REACTIONS
氰化氢- 维基百科，自由的百科全书
An overview on the progress and development on metals/non-metal catalyzed cyanation reactions - ScienceDirect
Non-toxic cyanide sources and cyanating agents - Organic
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Unrivale Label, non toxic, non, toxic icon - Download on Iconfinder, non-toxic
Recent Advancement on the Indirect or Combined Alternative Thiocyanate Sources for the Construction of S−CN Bonds - Karmaker - The Chemical Record - Wiley Online Library
(PDF) An overview on the progress and development on metals/non-metal catalyzed cyanation reactions
Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos-Ni(I) species. - Abstract - Europe PMC
Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos–Ni(I) species
In Situ Generated Magnesium Cyanide as an Efficient Reagent for Nucleophilic Cyanation of Nitrosoalkenes and Parent Nitronates - Ushakov - 2019 - European Journal of Organic Chemistry - Wiley Online Library
Fabrication of Pd Nanoparticles Embedded C@Fe3O4 Core–Shell Hybrid
