Author:
Weygand F.,Steglich W.,Fraunberger F.
Subject
General Chemistry,Catalysis
Reference5 articles.
1. Part VII of N-Acyltrihalogenoacetaldimines as Reactive Intermediates in Elimination-Addition-Reactions. – Part VI: , , and , Chem. Ber., in press.
2. Über einen ungewöhnlich leichten Austausch der Sulfonylgruppe gegen nucleophile Reste bei 2.2.2‐Trifluor‐1‐äthansulfonyl‐
N
‐acyl‐äthylaminen
3. Synthese von 3,3,3-Trifluoralanin und 3,3,3-Trifluoralanylpeptiden
4. Synthesis of 3,3,3-Trifluoroalanine and of 3,3,3-Trifluoroalanyl Peptides
5. N
‐Acyl‐trihalogenacetaldimine als reaktive Zwischenstufen bei Eliminierungs‐Additions‐Reaktionen, III. Darstellung und Reaktionen der 1.2.2.2‐Tetrahalogen‐
N
‐acyl‐äthylamine
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1. Synthetic strategies to α-trifluoromethyl and α-difluoromethyl substituted α-amino acids;Chemical Society Reviews;2008
2. Synthese Simple des Analogues Fluores, Phosphones ou Sulfones de L'Acide Aspartique;Phosphorus, Sulfur, and Silicon and the Related Elements;2007-02-15
3. An asymmetric synthesis of both enantiomers of 2,2,2-trifluoro-1-furan-2-yl-ethylamine and 3,3,3-trifluoroalanine from 2,2,2-trifluoro-1-furan-2-yl-ethanone;Tetrahedron: Asymmetry;2001-09
4. Asymmetric reduction of 2-(N-arylimino)-3,3,3-trifluoropropanoic acid esters leading to enantiomerically enriched 3,3,3-trifluoroalanine;Tetrahedron;1996-01
5. Benzotriazole-assisted synthesis of α-acylaminonitriles and a conceptually novel method for peptide elongation;J. Chem. Soc., Perkin Trans. 1;1990