Non-toxic cyanide sources and cyanating agents - Organic

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

Metal-Free Aerobic Oxidative Cyanation of Tertiary Amines: Azobis(isobutyronitrile) (AIBN) as a Sole Cyanide Source.

Non-toxic cyanide sources and cyanating agents - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02140F

Fabrication of Pd Nanoparticles Embedded C@Fe3O4 Core–Shell Hybrid

Rhodium catalyzed cyanide-free cyanation of aryl halide by using formamide as a cyanide source - ScienceDirect

Photochemically Induced Radical Transformation of C(sp3)–H Bonds

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

Cyanation - an overview

Fabrication of Pd Nanoparticles Embedded C@Fe3O4 Core–Shell Hybrid

Non-toxic cyanide sources and cyanating agents - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02140F

PDF) Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos–Ni(I) species

Non-toxic cyanide sources and cyanating agents - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02140F