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Angewandte Chemie International Edition, ISSN 1433-7851, 02/2014, Volume 53, Issue 8, pp. 2186 - 2189
Journal Article
by Chen, H and Sun, SH and Liu, YA and Liao, XB
ACS CATALYSIS, ISSN 2155-5435, 01/2020, Volume 10, Issue 2, pp. 1397 - 1405
We report nickel-catalyzed cyanation and hydrocyanation methods to prepare aryl nitriles and vinyl nitriles from aryl halides and alkynes, respectively. Using... 
PALLADIUM | hydrocyanation | ACTIVATION | PHOTOREDOX | H CYANATION | CONJUGATE CYANATION | CHEMISTRY, PHYSICAL | DECARBONYLATIVE CYANATION | CARBON-CARBON BONDS | Markovnikov addition | OXIDATIVE CYANATION | nickel catalysis | MILD | cyanation | Z/E selectivity | C-CN bond cleavage | STRECKER REACTION
Journal Article
Organic & Biomolecular Chemistry, ISSN 1477-0520, 2019, Volume 17, Issue 1, pp. 11 - 23
The present review gives an overview over non-toxic cyanation agents and cyanide sources used in the synthesis of structurally diverse products containing the... 
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2019, Volume 17, Issue 1, pp. 11 - 23
The present review gives an overview over non-toxic cyanation agents and cyanide sources used in the synthesis of structurally diverse products containing the... 
EFFICIENT HETEROGENEOUS CATALYST | C-H CYANATION | ELECTROPHILIC CYANATION | COPPER-MEDIATED CYANATION | LIGAND-FREE | ARYL HALIDES | CHEMISTRY, ORGANIC | POTASSIUM HEXACYANOFERRATE(II) | BETA-KETO-ESTERS | PALLADIUM-CATALYZED CYANATION | PHENYL-P-TOLUENESULFONAMIDE | Cyanide | Cyanides
Journal Article
ACS Catalysis, ISSN 2155-5435, 09/2016, Volume 6, Issue 9, pp. 5989 - 6005
The cyano group is well known as a versatile intermediate for transformations into a multitude of useful functional groups such as carboxyl, carbamoyl,... 
and cyano-group sources | cyanation | benzonitriles | arenes | α-aminonitriles | TERTIARY-AMINES | CYANO SOURCE | CHEMISTRY, PHYSICAL | alpha-aminonitriles | DIRECT TRANSFORMATION | COUPLING REACTIONS | RHODIUM-CATALYZED CYANATION | SODIUM-CYANIDE | BENZYL CYANIDE | RECENT PROGRESS | DIRECT OXIDATIVE CYANATION | PHENYL-P-TOLUENESULFONAMIDE
Journal Article
Tetrahedron, ISSN 0040-4020, 01/2019, Volume 75, Issue 2, pp. 308 - 314
One-step base promoted strategy for cyanation of α,α-diaryl alcohols has been developed under mild and transition metal-free conditions. This method provides a... 
Cyanation | Dual activity | Diarylalcohols
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2019, Volume 361, Issue 21, pp. 4914 - 4918
Lewis acid‐mediated cyanation of phenol derivatives with N‐cyano‐N‐phenyl‐p‐toluenesulfonamide (NCTS) has been developed. The reaction proceeded efficiently... 
Lewis acid | Phenols | Cyanation | N-Cyano-N-phenyl-p-toluenesulfonamide | ROUTE | RADICAL CYANATION | ELECTROPHILIC CYANATION | ACTIVATION | CHEMISTRY, ORGANIC | HALOGEN | ALKYL IODIDES | BENZONITRILES | MILD | ARYL | CHEMISTRY, APPLIED | PALLADIUM-CATALYZED CYANATION | Nitriles | Regioselectivity
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2012, Volume 51, Issue 48, pp. 11948 - 11959
Journal Article