Process for the synthesis of chirally pure beta-amino-alcohols
A process is provided for preparing chirally pure S-enantiomers of α-amino acids comprising the steps of: a) preparing an organometallic reagent from an alkyl halide of the formula (R)2CH(CH2)nCH2X; b) adding th
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(2008/06/13)
Production of chirally pure α-amino acids and N-sulfonyl α-amino acids
Methods for production of chirally pure α-amino acids and N-sulfonyl α-amino acids are described. An aldehyde and a cyanide salt are reacted with an α-methylbenzylamine to afford product. The product reacts with a strong acid, neutralized, and extracted.
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Page column 21
(2008/06/13)
Synthesis of L α amino acids structurally related to isoleucine
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Praetorius,Flossdorf,Kula
p. 3079 - 3090
(2007/10/05)
Stereochemical aspects of lotaustralin biosynthesis
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Zilg,Conn
p. 3112 - 3115
(2007/10/05)
The synthesis of tenuazonic and congeneric tetramie acids.
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Harris,Fisher,Folkers
p. 478 - 482
(2007/10/05)
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