Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction

Dietz FR, Gröger H (2008)
SYNLETT 2008(5): 663-666.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Abstract / Bemerkung
A short synthetic route to protected alpha-methyl threonine 5 as a representative example for (protected) alpha-methylated alpha-amino-beta-hydroxy acids bearing a stereogenic quaternary carbon center in a-position was developed. This multistep synthesis is based on the use of an easily accessible prochiral starting material in the presence of an organocatalyst, and allows the access to all four types of stereoisomers. In addition, the first enantioselective acetyl migration in a Steglich rearrangement reaction as a key step in this multistep synthesis of 5 was achieved. The heterocycle 12, which was used in Steglich rearrangement reaction for the first time, turned out to be an efficient organocatalyst leading to an enantioselectivity of up to 63% ee.
Erscheinungsjahr
Zeitschriftentitel
SYNLETT
Band
2008
Zeitschriftennummer
5
Seite
663-666
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Dietz FR, Gröger H. Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT. 2008;2008(5):663-666.
Dietz, F. R., & Gröger, H. (2008). Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT, 2008(5), 663-666. doi:10.1055/s-2008-1032104
Dietz, F. R., and Gröger, H. (2008). Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT 2008, 663-666.
Dietz, F.R., & Gröger, H., 2008. Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT, 2008(5), p 663-666.
F.R. Dietz and H. Gröger, “Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction”, SYNLETT, vol. 2008, 2008, pp. 663-666.
Dietz, F.R., Gröger, H.: Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction. SYNLETT. 2008, 663-666 (2008).
Dietz, Friedrich R., and Gröger, Harald. “Novel catalytic synthetic route to protected alpha-methyl threonine and the first asymmetric acetyl migration in a Steglich rearrangement reaction”. SYNLETT 2008.5 (2008): 663-666.