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Nitriles cyano

Ketones Nitriles (cyano compounds) Sulfides Thiols... [Pg.466]

The indium hydride compound, generated in situ from sodium borohydride and a catalytic amount of indium(m) chloride, selectively reduces carbon-carbon double bonds in conjugated alkenes such as a,a-dicyano olefins, a,/3-unsaturated nitriles, cyano esters, cyanophosphonates, diesters, and ketones (Scheme 107).372 This combined reagent system in acetonitrile reduces exclusively the a,/3-carbon-carbon double bond in a,/3,7,<5-unsaturated diaryl ketones, dicarboxylic esters, cyano esters, and dicyano compounds (Scheme 108).373... [Pg.715]

How would you explain the reaction of Grignard reagent (R-Mg-X) on a carbonyl compound and a nitrile (cyano) compound ... [Pg.171]

This chapter explores several different carbon-carbon bond-forming reactions that lead to a variety of functionalized molecules diketones, hydroxy-ketones and hydroxy-aldehydes, keto-esters, keto-aldehydes, keto-nitriles, cyano-esters, hydroxy-nitriles, and cyano-aldehydes and cyano-ketones. The reactions that form these products may be categorized by defining the relevant disconnection. [Pg.1161]

Nitrile CH3CH2 c yj Propanenitrrle Ethyl cyanide -nitrile cyano-... [Pg.1265]

Amine, Alcohol, Aldehyde, Alkane, Alkene, Alkyl Halide, Alkyne, Carboxylic Acid, Epoxide, Ether, Ketone, Nitrile (cyano), Nitro, Phenyl Group (benzene ring) and Thiol. [Pg.252]

See other pages where Nitriles cyano is mentioned: [Pg.49] [Pg.430] [Pg.477] [Pg.397] [Pg.492] [Pg.988] [Pg.1287] [Pg.236] [Pg.95] [Pg.1179] [Pg.592] [Pg.510] [Pg.300] [Pg.129] [Pg.196] [Pg.21] [Pg.733] [Pg.34] [Pg.279] [Pg.984] [Pg.41] [Pg.122] [Pg.3730] [Pg.118] [Pg.179] [Pg.2573] [Pg.288] [Pg.24] [Pg.487] [Pg.1183] [Pg.791] [Pg.430] [Pg.6] [Pg.359] [Pg.104]

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Cyano and Nitrile Complexes

Cyano functional group, nitriles

Cyano group of nitriles

Cyano ketones, from nitriles

Cyano-ketones => nitriles

Cyano-substituted nitrile ylides