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

SciELO - Brazil - RECENT ADVANCES IN CYANATION REACTIONS ^{RECENT ADVANCES IN CYANATION REACTIONS}

SciELO - Brazil - RECENT ADVANCES IN CYANATION REACTIONS ^{RECENT ADVANCES IN CYANATION REACTIONS}

Publications Organic Chemistry

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

Rapid ecosynthesis of TiO2@CuO@Chromite nanocatalyst for environmentally friendly applications: solventless cyanation of aldehydes and high efficient treatment of sewage waters, Environmental Sciences Europe

Natural halloysite nanotubes as an efficient catalyst in strecker reaction: the synthesis of α-amino nitriles under solvent-free conditions

Copper-Mediated Transformation of Organosilanes to Nitriles with

Give you more choice Non toxic product stock vector. Illustration

Stable palladium nanoparticles catalyzed synthesis of benzonitriles using K4[Fe(CN)6] - ScienceDirect

Development of Pd/C-Catalyzed Cyanation of Aryl Halides

Development of Decarboxylative Cyanation Reactions for C-13/C-14 Carboxylic Acid Labeling Using an Electrophilic Cyanating Reagent

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

Recent catalytic cyanation reactions using alkylnitriles

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

A Review on Metal-Free Oxidative α-Cyanation and Alkynylation of N-Substituted Tetrahydroisoquinolines as a Rapid Route for the Synthesis of Isoquinoline Alkaloids