ChemInform Abstract: REDUCTIVE ALKYLATION OF β-ALKANOLAMINES WITH CARBONYL COMPOUNDS AND SODIUM BOROHYDRIDE

1985 ◽  
Vol 16 (43) ◽  
Author(s):  
J. E. SAAVEDRA
2002 ◽  
Vol 80 (7) ◽  
pp. 779-788 ◽  
Author(s):  
Giancarlo Verardo ◽  
Paola Geatti ◽  
Elena Pol ◽  
Angelo G Giumanini

α-Amino acids and α-amino methyl esters are easily converted to their N-monoalkyl derivatives by a reductive condensation reaction using several carbonyl compounds in the presence of sodium borohydride. This reducing agent has shown a wide versatility with minor but essential procedural variations. The reaction allows the α-monodeuterium labeling of the new N-substituent by use of sodium borodeuteride.Key words: α-amino acid, α-amino methyl esters, sodium borohydride, reductive N-monoalkylation, carbonyl compounds.


2010 ◽  
Vol 40 (7) ◽  
pp. 951-956 ◽  
Author(s):  
Heshmatollah Alinezhad ◽  
Mahmood Tajbakhsh ◽  
Nastaran Mahdavi

Synthesis ◽  
2010 ◽  
Vol 2011 (03) ◽  
pp. 490-496 ◽  
Author(s):  
Mahmood Tajbakhsh ◽  
Rahman Hosseinzadeh ◽  
Heshmatollah Alinezhad ◽  
Somayeh Ghahari ◽  
Akbar Heydari ◽  
...  

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