Explore: Isocyanides

structure and is responsible of the linearity of isocyanides, although the reactivity of isocyanides reflects some carbene character, at least in a formal

the smell of methyl isocyanide, like that of other simple volatile isocyanides, is distinctly penetrating and vile. Methyl isocyanide is mainly used for

π-acceptor than CO and νNO is a diagnostic tool in metal–nitrosyl chemistry. Isocyanides, RNC, are another class of ligands that are capable of π-backbonding

Transition metal isocyanide complexes are coordination compounds containing isocyanide ligands. Several thousand isocyanides are known, but the coordination

reaction, by the reaction of various ketones (or aldehydes), amines, isocyanides and carboxylic acids. These libraries can then be tested with enzymes

The Nef isocyanide reaction is an addition reaction that takes place between isocyanides and acyl chlorides to form imidoyl chloride products, a process

CH3CH(O)CH2 + H2O + KCl The carbylamine reaction for the synthesis of isocyanides from the action of chloroform on a primary amine involves three dehydrohalogenations

yield and good enantioselectivities. For other types of isocyanides, rate of addition of isocyanide to reaction mixture dictates good yields and high selectivities

[page needed][page needed] Isocyanates should not be confused with cyanate esters and isocyanides, very different families of compounds. The cyanate (cyanate ester) functional

as defined by the functional group C≡N-R. tert-Butyl isocyanide, like most alkyl isocyanides, is a reactive colorless liquid with an extremely unpleasant