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Amino acids nitrile metal complexes

The Strecker reaction [1] starting from an aldehyde, ammonia, and a cyanide source is an efficient method for the preparation of a-amino acids. A popular version for asymmetric purposes is based on the use of preformed imines 1 and a subsequent nucleophilic addition of HCN or TMSCN in the presence of a chiral catalyst [2], Besides asymmetric cyanations catalyzed by metal-complexes [3], several methods based on the use of organocatalysts have been developed [4-14]. The general organocatalytic asymmetric hydrocyanation reaction for the synthesis of a-amino nitriles 2 is shown in Scheme 5.1. [Pg.85]


See other pages where Amino acids nitrile metal complexes is mentioned: [Pg.37]    [Pg.599]    [Pg.265]    [Pg.1087]    [Pg.613]    [Pg.869]    [Pg.194]    [Pg.194]    [Pg.246]    [Pg.489]    [Pg.2149]    [Pg.26]    [Pg.58]    [Pg.117]    [Pg.170]    [Pg.194]    [Pg.237]    [Pg.869]    [Pg.494]    [Pg.59]    [Pg.2148]    [Pg.911]    [Pg.7014]    [Pg.113]    [Pg.147]    [Pg.28]    [Pg.192]    [Pg.148]    [Pg.304]    [Pg.17]    [Pg.54]    [Pg.100]    [Pg.205]    [Pg.273]    [Pg.205]    [Pg.109]    [Pg.90]   
See also in sourсe #XX -- [ Pg.2 , Pg.265 ]




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0-Amino nitriles

7-Amino- -nitril

Amino acid complexes

Amino acids metal complexes

Amino complex

Metal complexes acidity

Metal nitriles

Metalated nitrile

Metalation nitriles

Metall-amino

Nitriles acidity

Nitriles complexes

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