Structures of peptides from α-amino acids methylated at the α-carbon,
✍ Scribed by C. Toniolo; M. Crisma; F. Formaggio; C. Valle; G. Cavicchioni; G. Precigoux; A. Aubry; J. Kamphuis
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1993
- Tongue
- English
- Weight
- 923 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0006-3525
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## Abstract A new route to completely protected α‐methylated α‐amino acids starting from alanine is described (see __Scheme__). These derivatives, which are obtained __via__ base‐catalyzed opening of the oxazolidinones (2__S__,4__R__)‐ and (2__R__,4__S__)‐2, can be directly employed in peptide synt
The lipophilic, chiral, C h -methylated h-amino acid L-(h Me)Aoc (2-methyl-2-amino-octanoic acid) was prepared using a chemo-enzymatic approach. Two series of terminally protected model peptides, from dimer through to hexamer, containing L-(h Me)Aoc in combination with either Gly or Aib, were synthe
## Abstract For Abstract see ChemInform Abstract in Full Text.