Abstract α-Amino nitrile compounds have a profound impact on bio-chemical sciences, as
they have been prepared from inexpensive starting materials and have become valuable …

Nitriles unveil widespread applications in pharmaceuticals, agrochemicals, textiles, rubber,
polymers, and constitute a significant intermediate in several organic transformations …

The cyano group is well known as a versatile intermediate for transformations into a
multitude of useful functional groups such as carboxyl, carbamoyl, aminomethyl, carbonyl …

The one-step conversion of aliphatic carboxylic acids to the corresponding nitriles has been
accomplished via the merger of visible light mediated photoredox and …

A new iridium‐catalyzed reductive Strecker reaction for the direct and efficient formation of α‐
amino nitrile products from a broad range of (hetero) aromatic and aliphatic tertiary amides …

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α-Aminonitriles, which have anticancer, antibacterial, antiviral, and antifungal properties,
have played an important role in pharmacology. Furthermore, they can also be used to …

Alkox-oxylactonization and dearomatization of 3′-hydroxy-[1, 1′-biphenyl]-2-carboxylic
acid simultaneously promoted by hypervalent iodine have been developed using …

A novel nitration (via C (sp3)–N breaking/C (sp2)–N formation with CH3NO2) mediated by
[bis (trifluoroacetoxy) iodo] benzene (PIFA) is described. The NO2 transfer from CH3NO2 to …

Metal-free electrochemical oxidation cyanation and phosphonylation reactions had been
developed, in which 2, 2, 6, 6-tetramethylpiperidinyl-N-oxyl (TEMPO) reduced the electrode …