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pro vyhledávání: '"J. Constanze D. Müller-Hartwieg"'
Autor:
Markus Furegati, Cara E. Brocklehurst, Flavio Ossola, Luigi La Vecchia, J. Constanze D. Müller-Hartwieg
Publikováno v:
Helvetica Chimica Acta. 93:314-323
α-Aminomethylation of (R)-DIOZ-alkylated (DIOZ=4-isopropyl-5,5-diphenyloxazolidin-2-one) substrates is a key step in the asymmetric synthesis of β2-amino acids, but it is unfortunately often accompanied by formation of transcarbamation by-products.
Autor:
Cara E. Humphrey, Thomas Leutert, Markus Furegati, Kurt Laumen, Markus Vögtle, Luigi La Vecchia, J. Constanze D. Müller-Hartwieg
Publikováno v:
Organic Process Research & Development. 11:1069-1075
This paper demonstrates how l-m-tyrosine 1 can be synthesized on larger-scale via enzyme-catalyzed kinetic resolution of N-acyl m-tyrosine methyl ester 4. N-Acyl m-tyrosine methyl ester 4 was prepared by a modification of Erlenmeyer’s azalactone sy
Publikováno v:
Journal of Peptide Science. 9:187-199
The synthesis of heterocyclic compounds containing the 7-membered ring system [1,4]diazepane-2,5-dione is described. The aim of this study was to elaborate the solid phase and solution synthesis of eight representatives of the cyclic scaffold and to
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 9(3)
The synthesis of heterocyclic compounds containing the 7-membered ring system [1,4]diazepane-2,5-dione is described. The aim of this study was to elaborate the solid phase and solution synthesis of eight representatives of the cyclic scaffold and to
Autor:
Cara E. Humphrey, Markus Furegati, Kurt Laumen, Luigi La Vecchia, Thomas Leutert, J. Constanze D. Müller-Hartwieg, Markus Vögtle
Publikováno v:
Organic Process Research & Development; Oct2007, Vol. 11 Issue 6, p1069-1075, 7p
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