Non-toxic cyanide sources and cyanating agents - Organic
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Description
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
Eco-friendly conjugate hydrocyanation of [alpha]-cyanoacrylates using potassium hexacyanoferrate(II) as cyanating reagent - Document - Gale Academic OneFile
Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos-Ni(I) species. - Abstract - Europe PMC
α‐Cyanation of Aromatic Tertiary Amines using Malononitrile as a Low‐Toxic Cyanide Source under the Catalysis of NiGa Layered Double Oxide - Wang - 2020 - Asian Journal of Organic Chemistry - Wiley Online Library
CN101717350B - Synthetic method of aryl cyanide in water solution - Google Patents
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Metal-Free Aerobic Oxidative Cyanation of Tertiary Amines: Azobis(isobutyronitrile) (AIBN) as a Sole Cyanide Source.
Compound Interest: The Chemistry of Poisons – Cyanide
Metal-Free Aerobic Oxidative Cyanation of Tertiary Amines: Azobis(isobutyronitrile) (AIBN) as a Sole Cyanide Source.
An overview on the progress and development on metals/non-metal catalyzed cyanation reactions - ScienceDirect
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Recent Advancement on the Indirect or Combined Alternative Thiocyanate Sources for the Construction of S−CN Bonds - Karmaker - The Chemical Record - Wiley Online Library
Non-toxic cyanide sources and cyanating agents - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02140F
Non-toxic cyanide sources and cyanating agents - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02140F
11C-, 12C-, and 13C-cyanation of electron-rich arenes via organic photoredox catalysis - ScienceDirect
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